U.S. patent application number 16/870851 was filed with the patent office on 2021-01-28 for methods of diagnosing a disease and methods of monitoring treatment of a disease by quantifying a non-reducing end glycan residual compound and comparing to a second biomarker.
This patent application is currently assigned to BIOMARIN PHARMACEUTICAL INC.. The applicant listed for this patent is BIOMARIN PHARMACEUTICAL INC.. Invention is credited to Jim R. BEITEL, Jillian R. BROWN, Brett E. CRAWFORD, Charles A. GLASS, Robin M. JACKMAN.
Application Number | 20210025874 16/870851 |
Document ID | / |
Family ID | 1000005137132 |
Filed Date | 2021-01-28 |
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United States Patent
Application |
20210025874 |
Kind Code |
A1 |
CRAWFORD; Brett E. ; et
al. |
January 28, 2021 |
METHODS OF DIAGNOSING A DISEASE AND METHODS OF MONITORING TREATMENT
OF A DISEASE BY QUANTIFYING A NON-REDUCING END GLYCAN RESIDUAL
COMPOUND AND COMPARING TO A SECOND BIOMARKER
Abstract
Provided herein are methods of diagnosing or monitoring the
treatment of abnormal glycan accumulation or a disorder associated
with abnormal glycan accumulation.
Inventors: |
CRAWFORD; Brett E.; (Poway,
CA) ; BROWN; Jillian R.; (Poway, CA) ; GLASS;
Charles A.; (Novato, CA) ; BEITEL; Jim R.;
(Novato, CA) ; JACKMAN; Robin M.; (San Diego,
CA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
BIOMARIN PHARMACEUTICAL INC. |
Novato |
CA |
US |
|
|
Assignee: |
BIOMARIN PHARMACEUTICAL
INC.
Novato
CA
|
Family ID: |
1000005137132 |
Appl. No.: |
16/870851 |
Filed: |
May 8, 2020 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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15892409 |
Feb 8, 2018 |
10677786 |
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16870851 |
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15097218 |
Apr 12, 2016 |
9915649 |
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15892409 |
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14462285 |
Aug 18, 2014 |
9340822 |
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15097218 |
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13629321 |
Sep 27, 2012 |
8809009 |
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14462285 |
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13550106 |
Jul 16, 2012 |
8771974 |
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13629321 |
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12649110 |
Dec 29, 2009 |
8232073 |
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13550106 |
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61561698 |
Nov 18, 2011 |
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61238079 |
Aug 28, 2009 |
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61164365 |
Mar 27, 2009 |
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61142291 |
Jan 2, 2009 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
C12Q 1/42 20130101; C12Q
1/40 20130101; G01N 2800/56 20130101; G01N 33/5308 20130101; G01N
2400/00 20130101; G01N 2800/044 20130101; C12Q 1/527 20130101; G01N
2333/988 20130101; G01N 2333/924 20130101; G01N 2400/10 20130101;
G01N 2800/042 20130101; G01N 2800/52 20130101; G01N 2800/04
20130101; C12Q 1/34 20130101; G01N 33/6893 20130101; G01N 2800/28
20130101 |
International
Class: |
G01N 33/53 20060101
G01N033/53; C12Q 1/34 20060101 C12Q001/34; C12Q 1/40 20060101
C12Q001/40; G01N 33/68 20060101 G01N033/68; C12Q 1/42 20060101
C12Q001/42; C12Q 1/527 20060101 C12Q001/527 |
Claims
1.-26. (canceled)
27. A method of determining in an individual the presence,
identity, and/or severity of mucopolysaccharidosis (MPS) III, the
method comprising: (a) generating a first biomarker comprising a
glycan residual compound, wherein the first biomarker is generated
by treating a population of glycans, in or isolated from a
biological sample from the individual, with at least one digesting
glycan enzyme, wherein prior to enzyme treatment, the first
biomarker is not present in abundance in samples from individuals
with MPS III relative to individuals without MPS III, and wherein
the first biomarker is a non-reducing end (NRE) biomarker; (b)
generating a second biomarker comprising a glycan residual
compound, wherein the second biomarker is generated by treating a
population of glycans, in or isolated from a biological sample from
the individual, with at least one digesting glycan enzyme, wherein
prior to enzyme treatment, the second biomarker is not present in
abundance in samples from individuals with the MPS III relative to
individuals without the MPS III, and wherein: 1) the second
biomarker is a reducing end biomarker, 2) the second biomarker is
an internal glycan biomarker, or 3) when the MPS III is caused by
an abnormal function of a glycan degradation enzyme in the
individual, the second biomarker is generated by treating the first
biomarker with the glycan degradation enzyme that is functioning
abnormally in the individual; (c) detecting the presence of and/or
measuring the amount of the first and second biomarker produced and
displaying or recording the presence of or a measure of a
population of the first and second biomarkers by using an
analytical instrument; and (d) monitoring and/or comparing the
amounts of the first and second biomarkers in a biological sample;
wherein the presence of and/or measure of the amounts of the first
and second biomarkers are utilized to determine the presence,
identity, and/or severity of MPS III.
28. The method of claim 27, wherein the population of glycans
comprises a glycan selected from the group consisting of
chondroitin sulfate, dermatan sulfate, and heparan sulfate.
29. The method of claim 27, wherein the MPS is MPS IIIA, MPS IIIB,
MPS IIIC, or MPS IIID, and wherein: a. when the MPS is MPS IIIA,
first biomarker is selected from the group consisting of GlcNS,
GlcNS6S-UA2S-GlcNAc6S, GlcNS-UA-GlcNAc, GlcNS-UA2S-GlcNAc6S,
GlcNS6S-UA-GlcNAc6S, GlcNS6S-UA2S-GlcNAc, GlcNS6S-UA-GlcNAc,
GlcNS-UA2S-GlcNAc, GlcNS, GlcNS-UA-GlcNAc6S, GlcNS6S-UA2S-GlcNS6S,
GlcNS-UA-GlcNS, GlcNS-UA2S-GlcNS6S, GlcNS6S-UA-GlcNS6S,
GlcNS6S-UA2S-GlcNS, GlcNS6S-UA-GlcNS, GlcNS-UA2S-GlcNS, GlcNS,
GlcNS-UA-GlcNS6S; b. when the MPS is MPS IIIB, first biomarker is
selected from the group consisting of GlcNAc, GlcNAc-UA2S-GlcNAc6S,
GlcNAc-UA-GlcNAc, GlcNAc-UA2S-GlcNAc, GlcNAc-UA-GlcNAc6S,
GlcNAc-UA2S-GlcNS6S, GlcNAc-UA-GlcNS, GlcNAc-UA2S-GlcNS,
GlcNAc-UA-GlcNS6S; c. when the MPS is MPS IIIC, first biomarker is
selected from the group consisting of GlcN, GlcN6S-UA2S-GlcNAc6S,
GlcN-UA-GlcNAc, GlcN-UA2S-GlcNAc6S, GlcN6S-UA-GlcNAc,
GlcN6S-UA2S-GlcNAc, GlcN6S-UA-GlcNAc, GlcN-UA2S-GlcNAc,
GlcN-UA-GlcNAc6S, GlcN6S-UA2S-GlcNS6S, GlcN-UA-GlcNS,
GlcN-UA2S-GlcNS6S, GlcN6S-UA-GlcNS6S, GlcN6S-UA2S-GlcNS,
GlcN6S-UA-GlcNS, GlcN-UA2S-GlcNS, GlcN-UA-GlcNS6S; and d. when the
MPS is MPS IIID, first biomarker is selected from the group
consisting of GlcN6S, GlcNAc6S, GlcN6S-UA2S-GlcNAc6S,
GlcN6S-UA-GlcNAc, GlcN6S-UA2S-GlcNAc, GlcN6S-UA-GlcNAc6S.
GlcNAc6S-UA2S-GlcNAc6S, GlcNAc6S-UA-GlcNAc, GlcNAc6S-UA2S-GlcNAc,
GlcNAc6S-UA-GlcNAc6S, GlcN6S-UA2S-GlcNS6S, GlcN6S-UA-GlcNS,
GlcN6S-UA2S-GlcNS, GlcN6S-UA-GlcNS6S, GlcNAc6S-UA2S-GlcNS6S,
GlcNAc6S-UA-GlcNS, GlcNAc6S-UA2S-GlcNS, GlcNAc6S-UA-GlcNS6S.
30. The method of claim 29, wherein the MPS is MPS IIIA, and
wherein the first biomarker is selected from the group consisting
of GlcNS and GlcNS-UA2S, -GlcNS.
31. The method of claim 29, wherein the MPS is MPS IIIB, and
wherein the first biomarker is GlcNAc-UA2S-GlcNS.
32. The method of claim 29, wherein the MPS is MPS IIIC, and
wherein the first biomarker is selected from the group consisting
of GlcN-UA2S-GlcNS6S and GlcN6S-UA-GlcNS6S.
33. The method of claim 29, wherein the MPS is MPS IIID, and
wherein the first biomarker is GlcN6S.
34. The method of claim 27, wherein the MPS is MPS IIIA, MPS IIIB,
MPS IIIC, or MPS IIID, and wherein: a. when the MPS is MPS IIIA,
the second biomarker is selected from the group consisting of
GlcNS, GlcNS6S-UA2S-GlcNAc6S, GlcNS-UA-GlcNAc, GlcNS-UA2S-GlcNAc6S,
GlcNS6S-UA-GlcNAc6S, GlcNS6S-UA2S-GlcNAc, GlcNS6S-UA-GlcNAc,
GlcNS-UA2S-GlcNAc, GlcNS, GlcNS-UA-GlcNAc6S, GlcNS6S-UA2S-GlcNS6S,
GlcNS-UA-GlcNS, GlcNS-UA2S-GlcNS6S, GlcNS6S-UA-GlcNS6S,
GlcNS6S-UA2S-GlcNS, GlcNS6S-UA-GlcNS, GlcNS-UA2S-GlcNS, GlcNS,
GlcNS-UA-GlcNS6S, GlcN, GlcN6S-UA2S-GlcNAc6S, GlcN-UA-GlcNAc,
GlcN-UA2S-GlcNAc6S, GlcN6S-UA-GlcNAc, GlcN6S-UA2S-GlcNAc,
GlcN6S-UA-GlcNAc, GlcN-UA2S-GlcNAc, GlcN-UA-GlcNAc6S,
GlcN6S-UA2S-GlcNS6S, GlcN-UA-GlcNS, GlcN-UA2S-GlcNS6S,
GlcN6S-UA-GlcNS6S, GlcN6S-UA2S-GlcNS, GlcN6S-UA-GlcNS,
GlcN-UA2S-GlcNS, GlcN-UA-GlcNS6S, .DELTA.UA-GlcN, .DELTA.UA-GlcN6S,
.DELTA.UA2S-GlcN, .DELTA.UAS-GlcN6S, .DELTA.UA-GlcNAc,
.DELTA.UA-GlcNAc6S, .DELTA.UA2S-GlcNAc, .DELTA.UA2S-GlcNAc6S,
.DELTA.UA-GlcNS, .DELTA.UA-GlcNS6S, .DELTA.UA-GlcNS3S,
.DELTA.UA2S-GlcNS, .DELTA.UA2S-GlcNS6S, .DELTA.UA2S-GlcNS3S,
.DELTA.UA-GlcNS6S3S, .DELTA.UA2S-GlcNS6S3S, .DELTA.UA-GalNAc,
.DELTA.UA-GalNAc4S, .DELTA.UA-GalNAc6S, .DELTA.UA2S-GalNAc,
.DELTA.UA2S-GalNAc4S, .DELTA.UA2S-GalNAc6S, .DELTA.UA-GalNAc4S6S,
.DELTA.UA2S-GalNAc4S6S; b. when the MPS is MPS IIIB, the second
biomarker is selected from the group consisting of IdoA-GlcNS,
IdoA-GlcNS6S, IdoA-GlcNAc, IdoA-GlcNAc6S, IdoA-GalNAc4S,
IdoA-GalNAc6S, IdoA-GalNAc, IdoA-GalNAc4S6S, IdoA2S-GlcNS,
IdoA2S-GlcNS6S, IdoA2S-GlcNAc, IdoA2S-GlcNAc6S, IdoA2S-GalNAc4S,
IdoA2S-GalNAc6S, IdoA2S-GalNAc, IdoA2S-GalNAc4S6S GlcNAc,
GlcNAc-UA2S-GlcNAc6S, GlcNAc-UA-GlcNAc, GlcNAc-UA2S-GlcNAc,
GlcNAc-UA-GlcNAc6S, GlcNAc-UA2S-GlcNS6S, GlcNAc-UA-GlcNS,
GlcNAc-UA2S-GlcNS, GlcNAc-UA-GlcNS6S, GlcA-GlcNAc, GlcA-GlcNS,
GlcA-GlcNAc6S, GlcA-GlcNS6S, GlcA-GalNAc, GlcA-GalNAc4S,
GlcA-GalNAc6S, GlcA-GalNAc4S6S, Gal-GlcNAc, Gal-GlcNAc6S,
Gal6S-GlcNAc, Gal6S-GlcNAc6S, GlcNAc-Gal, GlcNAc-Gal6S,
GlcNAc6S-Gal, GlcNAc6S-Gal6S, .DELTA.UA-GlcN, .DELTA.UA-GlcN6S,
.DELTA.UA2S-GlcN, .DELTA.UAS-GlcN6S, .DELTA.UA-GlcNAc,
.DELTA.UA-GlcNAc6S, .DELTA.UA2S-GlcNAc, .DELTA.UA2S-GlcNAc6S,
.DELTA.UA-GlcNS, .DELTA.UA-GlcNS6S, .DELTA.UA-GlcNS3S,
.DELTA.UA2S-GlcNS, .DELTA.UA2S-GlcNS6S, .DELTA.UA2S-GlcNS3S,
.DELTA.UA-GlcNS6S3S, .DELTA.UA2S-GlcNS6S3S, .DELTA.UA-GalNAc,
.DELTA.UA-GalNAc4S, .DELTA.UA-GalNAc6S, .DELTA.UA2S-GalNAc,
.DELTA.UA2S-GalNAc4S, .DELTA.UA2S-GalNAc6S, .DELTA.UA-GalNAc4S6S,
.DELTA.UA2S-GalNAc4S6S; c. when the MPS is MPS IIIC, the second
biomarker is selected from the group consisting of GlcNAc,
GlcNAc-UA2S-GlcNAc6S, GlcNAc-UA-GlcNAc, GlcNAc-UA2S-GlcNAc,
GlcNAc-UA-GlcNAc6S, GlcNAc-UA2S-GlcNS6S, GlcNAc-UA-GlcNS,
GlcNAc-UA2S-GlcNS, GlcNAc-UA-GlcNS6S, GlcN, GlcN6S-UA2S-GlcNAc6S,
GlcN-UA-GlcNAc, GlcN-UA2S-GlcNAc6S, GlcN6S-UA-GlcNAc,
GlcN6S-UA2S-GlcNAc, GlcN6S-UA-GlcNAc, GlcN-UA2S-GlcNAc,
GlcN-UA-GlcNAc6S, GlcN6S-UA2S-GlcNS6S, GlcN-UA-GlcNS,
GlcN-UA2S-GlcNS6S, GlcN6S-UA-GlcNS6S, GlcN6S-UA2S-GlcNS,
GlcN6S-UA-GlcNS, GlcN-UA2S-GlcNS, GlcN-UA-GlcNS6S, .DELTA.UA-GlcN,
.DELTA.UA-GlcN6S, .DELTA.UA2S-GlcN, .DELTA.UAS-GlcN6S,
.DELTA.UA-GlcNAc, .DELTA.UA-GlcNAc6S, .DELTA.UA2S-GlcNAc,
.DELTA.UA2S-GlcNAc6S, .DELTA.UA-GlcNS, .DELTA.UA-GlcNS6S,
.DELTA.UA-GlcNS3S, .DELTA.UA2S-GlcNS, .DELTA.UA2S-GlcNS6S,
.DELTA.UA2S-GlcNS3S, .DELTA.UA-GlcNS6S3S, .DELTA.UA2S-GlcNS6S3S,
.DELTA.UA-GalNAc, .DELTA.UA-GalNAc4S, .DELTA.UA-GalNAc6S,
.DELTA.UA2S-GalNAc, .DELTA.UA2S-GalNAc4S, .DELTA.UA2S-GalNAc6S,
.DELTA.UA-GalNAc4S6S, .DELTA.UA2S-GalNAc4S6S; and d. when the MPS
is MPS IIID, the second biomarker is selected from the group
consisting of GlcNAc, GlcNAc-UA2S-GlcNAc6S, GlcNAc-UA-GlcNAc,
GlcNAc-UA2S-GlcNAc, GlcNAc-UA-GlcNAc6S, GlcNAc-UA2S-GlcNS6S,
GlcNAc-UA-GlcNS, GlcNAc-UA2S-GlcNS, GlcNAc-UA-GlcNS6S, GlcN,
GlcN6S-UA2S-GlcNAc6S, GlcN-UA-GlcNAc, GlcN-UA2S-GlcNAc6S,
GlcN6S-UA-GlcNAc6S, GlcN6S-UA2S-GlcNAc, GlcN6S-UA-GlcNAc,
GlcN-UA2S-GlcNAc, GlcN-UA-GlcNAc6S, GlcN6S-UA2S-GlcNS6S,
GlcN-UA-GlcNS, GlcN-UA2S-GlcNS6S, GlcN6S-UA-GlcNS6S,
GlcN6S-UA2S-GlcNS, GlcN6S-UA-GlcNS, GlcN-UA2S-GlcNS,
GlcN-UA-GlcNS6S, GlcN6S, GlcNAc6S, GlcN6S-UA2S-GlcNAc6S,
GlcN6S-UA-GlcNAc, GlcN6S-UA2S-GlcNAc, GlcN6S-UA-GlcNAc6S,
GlcNAc6S-UA2S-GlcNAc6S, GlcNAc6S-UA-GlcNAc, GlcNAc6S-UA2S-GlcNAc,
GlcNAc6S-UA-GlcNAc6S, GlcN6S-UA2S-GlcNS6S, GlcN6S-UA-GlcNS,
GlcN6S-UA2S-GlcNS, GlcN6S-UA-GlcNS6S, GlcNAc6S-UA2S-GlcNS6S,
GlcNAc6S-UA-GlcNS, GlcNAc6S-UA2S-GlcNS, GlcNAc6S-UA-GlcNS,
.DELTA.UA-GlcN, .DELTA.UA-GlcN6S, .DELTA.UA2S-GlcN,
.DELTA.UAS-GlcN6S, .DELTA.UA-GlcNAc, .DELTA.UA-GlcNAc6S,
.DELTA.UA2S-GlcNAc, .DELTA.UA2S-GlcNAc6S, .DELTA.UA-GlcNS,
.DELTA.UA-GlcNS6S, .DELTA.UA-GlcNS3S, .DELTA.UA2S-GlcNS,
.DELTA.UA2S-GlcNS6S, .DELTA.UA2S-GlcNS3S, .DELTA.UA-GlcNS6S3S,
.DELTA.UA2S-GlcNS6S3S, .DELTA.UA-GalNAc, .DELTA.UA-GalNAc4S,
.DELTA.UA-GalNAc6S, .DELTA.UA2S-GalNAc, .DELTA.UA2S-GalNAc4S,
.DELTA.UA2S-GalNAc6S, .DELTA.UA-GalNAc4S6S,
.DELTA.UA2S-GalNAc4S6S.
35. The method of claim 34, wherein the MPS is MPS IIIA, the first
biomarker is GlcNS, and the second biomarker is
GlcNS-UA2S-GlcNS.
36. The method of claim 34, wherein the MPS is MPS IIIC, and
wherein the first biomarker is GlcN-UA2S-GlcNS6S and the second
biomarker is GlcN6S-UA-GlcNS6S.
37. The method of claim 27, wherein the at least one digesting
glycan enzyme is selected from the group consisting of N-sulfatase,
heparin lyase, hexosaminidase, deacetylase, 6-O sulfatase, N-acetyl
glucosaminidase, glucosamine N-acetyltransferase and N-acetyl
transferase.
38. A method of determining in an individual the presence,
identity, and/or severity of mucopolysaccharidosis (MPS) III, the
method comprising: (a) generating a first biomarker comprising a
glycan residual compound, wherein the first biomarker is generated
by treating a population of glycans, in or isolated from a
biological sample from the individual, with at least one digesting
glycan enzyme, wherein prior to enzyme treatment, the first
biomarker is not present in abundance in samples from individuals
with MPS III relative to individuals without MPS III, and wherein
the first biomarker is a non-reducing end (NRE) biomarker; (b)
generating a second biomarker comprising a glycan residual
compound, wherein the second biomarker is generated by treating a
population of glycans, in or isolated from a biological sample from
the individual, with at least one digesting glycan enzyme, wherein
prior to enzyme treatment, the second biomarker is not present in
abundance in samples from individuals with the MPS III relative to
individuals without the MPS III, and wherein: 1) the second
biomarker is an NRE biomarker different from the first biomarker,
2) the second biomarker is a reducing end biomarker, 3) the second
biomarker is an internal glycan biomarker, or 4) when the MPS III
is caused by an abnormal function of a glycan degradation enzyme in
the individual, the second biomarker is generated by treating the
first biomarker with the glycan degradation enzyme that is
functioning abnormally in the individual; (c) detecting the
presence of and/or measuring the amount of the first and second
biomarker produced and displaying or recording the presence of or a
measure of a population of the first and second biomarkers by using
an analytical instrument; and (d) monitoring and/or comparing the
amounts of the first and second biomarkers in a biological sample;
wherein the presence of and/or measure of the amounts of the first
and second biomarkers are utilized to determine the presence,
identity, and/or severity of MPS III.
Description
CROSS-REFERENCE
[0001] This application is a divisional of U.S. application Ser.
No. 15/892,409, filed Feb. 8, 2018, which is a continuation
application of U.S. application Ser. No. 15/097,218, filed Apr. 12,
2016, now U.S. Pat. No. 9,915,649, issued on Mar. 13, 2018, which
is a continuation of U.S. application Ser. No. 14/462,285, filed
Aug. 18, 2014, now U.S. Pat. No. 9,340,822, issued on May 17, 2016,
which is a continuation of U.S. application Ser. No. 13/629,321,
filed Sep. 27, 2012, now U.S. Pat. No. 8,809,009, issued on Aug.
19, 2014, which claims the benefit of U.S. Provisional Application
No. 61/561,698, filed Nov. 18, 2011, and is a continuation-in-part
of U.S. application Ser. No. 13/550,106, filed Jul. 16, 2012, now
U.S. Pat. No. 8,771,974, issued on Jul. 8, 2014, which is a
continuation of U.S. application Ser. No. 12/649,110, filed Dec.
29, 2009, now U.S. Pat. No. 8,232,073, issued on Jul. 31, 2012,
which claims the benefit of U.S. Provisional Application No.
61/238,079, filed Aug. 28, 2009, U.S. Provisional Application No.
61/164,365, filed Mar. 27, 2009, and U.S. Provisional Application
No. 61/142,291, filed Jan. 2, 2009; each of which is incorporated
by reference herein in its entirety.
BACKGROUND OF THE INVENTION
[0002] Many human diseases are caused by or correlated with changes
in glycosylation. In order to use these changes as biomarkers of
disease, analytical methods are used to quantify the changes. The
published methods use antibodies, chromatography and/or mass
spectrometry techniques to resolve and quantify the intact or
partially intact glycans. These methods are challenging due to the
complexity and number of possible glycan structures present in
biological samples. In a single disease state there can be
thousands of different novel glycan structures that are present;
however, each on their own is a weak marker of disease.
SUMMARY OF THE INVENTION
[0003] Described herein are populations of glycans that are
transformed into populations of biomarkers using glycan degradation
enzymes. In some embodiments, described herein are populations of
glycosaminoglycans that are transformed into populations of
oligosaccharides using glycosaminoglycan lyases. Further described
herein are the use of analytical instruments to characterize the
population of biomakers (i.e., non-reducing end glycan residual
compounds, such as monosaccharides) in order to provide relevant
information about the population of biomarkers, the population of
biomarkers and the biological sample that provided the population
of biomarkers. In some embodiments, described herein are the use of
analytical instruments to characterize the population of
oligosaccharides in order to provide relevant information about the
population of oligosaccharides, the population of
glycosaminoglycans and the biological sample that provided the
population of glycosaminoglycans.
[0004] Provided in certain embodiments herein are methods of
detecting glycan accumulation and/or abnormal glycan biosynthesis
and/or degradation in a biological sample, the method comprising:
[0005] a. transforming a glycan of a biological sample with a
glycan degradation enzyme to liberate a glycan residual compound
from the non-reducing end of the glycan; [0006] b. measuring the
amount of the glycan residual compound liberated by the functioning
glycan degradation enzyme with an analytical device.
[0007] In some embodiments, a method described herein comprises a
method of diagnosing an individual as having a disease or condition
associated with abnormal glycan biosynthesis, degradation, or
accumulation, the method comprising: [0008] a. generating a
biomarker comprising of one or more non-reducing end glycan
residual compound, wherein the biomarker is generated by treating a
population of glycans, in or isolated from a biological sample from
the individual, with at least one digesting glycan enzymes, wherein
prior to enzyme treatment, the biomarker is not present in
abundance in samples from individuals with the disease or condition
relative to individuals without the disease or condition, and
[0009] b. using an analytical instrument to detect the presence of
and/or measure the amount of the biomarker produced and displaying
or recording the presence of or a measure of a population of the
biomarker.
[0010] In some embodiments, the presence of and/or measure the
amount of the biomarker is utilized to determine the presence,
identity, and/or severity of the disease or condition.
[0011] Provided in certain embodiments herein is a method of
diagnosing an individual as having a disease or condition
associated with abnormal glycan biosynthesis, degradation, or
accumulation, the method comprising: [0012] a. transforming a
glycan of a biological sample with a glycan degradation enzyme to
liberate a glycan residual compound from the non-reducing end of
the glycan; [0013] b. measuring the amount of the glycan residual
compound liberated by the functioning glycan degradation enzyme
with an analytical device; and [0014] c. determining whether the
amount of liberated glycan residue is abnormal.
[0015] In some embodiments, provided herein is a method of
monitoring the treatment of a disorder associated with the abnormal
degradation, biosynthesis and/or accumulation of glycans, the
method comprising: [0016] a. following administration of an agent
for treating a disorder associated with the abnormal degradation,
biosynthesis and/or accumulation of glycans to an individual in
need thereof, using an analytical instrument to measure the amount
of a population of a biomarker comprising a non-reducing end glycan
residual compounds present in a transformed biological sample, the
biomarker being generated by treating a population of glycans, in
or isolated from a biological sample from the individual, with at
least one digesting glycan enzyme(s), wherein prior to enzyme
treatment, the biomarker is not present in abundance in samples
from individuals with the disease or condition relative to
individuals without the disease or condition, and [0017] b.
determining whether or not the amount of biomarker has decreased or
increased at a slower rate compared to the amount or rate of
increase prior to administration of the agent for treating a
disorder associated with the abnormal degradation, biosynthesis
and/or accumulation of glycans.
[0018] In some embodiments, the disorder associated with the
abnormal degradation, biosynthesis and/or accumulation of glycans
is a lysosomal storage disease, a cancerous disease, an
inflammatory disease, an infectious disease, a central nervous
system disease, or a cardiovascular disease. In some embodiments,
the normally functioning glycan degradation enzyme is a
glycosidase, sulfatase, phosphorylase, deacetylase, or a
combination thereof. In some embodiments, the normally functioning
glycan degradation enzyme is a glycosidase is selected from an
exo-glycosidase and an endo-glycosidase. In some embodiments, the
glycan residual compound is a monosaccharide, sulfate, phosphate,
acetate, or a combination thereof.
[0019] In some embodiments, transforming a glycan of a biological
sample with a normally functioning glycan degradation enzyme
comprises transforming a glycan of a biological sample with a
plurality of normally functioning glycan degradation enzymes. In
some embodiments, the glycan is treated with a plurality of
normally functioning glycan degradation enzymes concurrently,
sequentially, or a combination thereof. In some embodiments, prior
to measuring the amount of a population of non-reducing end glycan
residual compounds, the non-reducing end glycan residual compounds
are labeled with a detectable label. In some embodiments, the
detectable label is a mass label, a radioisotope label, a
fluorescent label, a chromophore label, or affinity label. In some
embodiments, the amount of liberated glycan is measured using
UV-Vis spectroscopy, IR spectroscopy, mass spectrometry, or a
combination thereof.
[0020] Provided in certain embodiments herein is a method of
diagnosing an individual as having a disease or condition
associated with abnormal glycan biosynthesis, degradation, or
accumulation, the method comprising: [0021] a. generating a
biomarker comprising of one or more non-reducing end glycan
residual compound, wherein the biomarker is generated by treating a
population of glycans, in or isolated from a biological sample from
the individual, with at least one digesting glycan enzymes, wherein
prior to enzyme treatment, the biomarker is not present in
abundance in samples from individuals with the disease or condition
relative to individuals without the disease or condition, and
[0022] b. using an analytical instrument to detect the presence of
and/or measure the amount of the biomarker produced and displaying
or recording the presence of or a measure of a population of the
biomarker; wherein the presence of and/or measure the amount of the
biomarker is utilized to determine the presence, identity, and/or
severity of the disease or condition.
[0023] In some embodiments, the disease or disorder is caused by an
abnormally functioning glycan degradation enzyme and wherein the
abnormally functioning glycan degradation enzyme and the normally
functioning glycan degradation enzyme are of the same type. In some
embodiments, the abnormally functioning glycan degradation enzyme
functions abnormally as a result of being present in an abnormally
low amount, functioning improperly, or a combination thereof. In
some embodiments, the abnormal glycan accumulation comprises the
accumulation of abnormal amounts of glycans. In some embodiments,
the abnormal glycan accumulation comprises the accumulation of
abnormal amounts of normal glycans. In some embodiments, the
abnormal glycan accumulation comprises the accumulation of abnormal
amounts of abnormal glycans.
[0024] In some embodiments, the normally functioning glycan
degradation enzyme is a glycosidase, sulfatase, phosphorylase,
deacetylase, or a combination thereof. In some embodiments, the
normally functioning glycan degradation enzyme is a glycosidase
selected from an exo-glycosidase and an endo-glycosidase. In some
embodiments, the glycosidase is an exo-glycosidase selected from
the group consisting of a galactosidase, and a glucuronidase.
[0025] In some embodiments, the glycan residual compound is a
monosaccharide. In some embodiments, the glycan residual compound
is sulfate, phosphate, acetate, or a combination thereof. In some
embodiments, a biological sample is purified prior to transforming
a glycan thereof. In some embodiments, the process of purifying a
biological sample comprises removing monosaccharides therefrom,
removing sulfates therefrom, removing phosphates therefrom,
removing acetate therefrom, or a combination thereof. In some
embodiments, transforming a glycan of a biological sample with a
normally functioning glycan degradation enzyme comprises
transforming a glycan of a biological sample with a plurality of
normally functioning glycan degradation enzymes. In some
embodiments, the glycan is treated with a plurality of normally
functioning glycan degradation enzymes concurrently, sequentially,
or a combination thereof.
[0026] In some embodiments, the disorder associated with an
abnormal glycan accumulation is MPS I, MPS II, MPS IIIA, MPS IVA,
MPSVI, or Fabry Disease. In some embodiments, determining whether
the amount of liberated glycan residue is abnormal comprises
labeling the glycan residue with a detectable label and measuring
the amount of labeled glycan residue with an analytical instrument.
In some embodiments, the detectable label is a mass label, a
radioisotope label, a fluorescent label, a chromophore label, or
affinity label. In some embodiments, the amount of liberated glycan
is measured using UV-Vis spectroscopy, IR spectroscopy, mass
spectrometry, or a combination thereof.
[0027] Provided herein, in certain embodiments, is a method of
diagnosing an individual as having a disease or condition (e.g.,
associated with abnormal glycan biosynthesis, degradation, or
accumulation), the method comprising: [0028] a. generating a first
biomarker comprising a glycan residual compound, wherein the first
biomarker is generated by treating a population of glycans, in or
isolated from a biological sample from the individual, with at
least one digesting glycan enzyme, wherein prior to enzyme
treatment, the first biomarker is not present in abundance in
samples from individuals with the disease or condition relative to
individuals without the disease or condition, [0029] b. generating
a second biomarker comprising a glycan residual compound, wherein
the second biomarker is generated by treating a population of
glycans, in or isolated from a biological sample from the
individual, with at least one digesting glycan enzyme in the same
or different digestion step as provided in step (a), wherein prior
to enzyme treatment, the second biomarker is not present in
abundance in samples from individuals with the disease or condition
relative to individuals without the disease or condition, [0030] c.
using an analytical instrument to detect the presence of and/or
measure the amount of the first and second biomarker produced and
displaying or recording the presence of or a measure of a
population of the first and second biomarkers, and [0031] d.
monitoring and/or comparing the amounts of the first and second
biomarkers in a biological sample; wherein the presence of and/or
measure of the amounts of the first and second biomarkers are
utilized to determine the presence, identity, and/or severity of
the disease or condition.
[0032] In some embodiments, the first biomarker is a non-reducing
end glycan residual compound. In some embodiments, the disease or
disorder is caused by an abnormally functioning glycan degradation
enzyme and wherein the abnormally functioning glycan degradation
enzyme and the digesting glycan enzyme are of the same type. In
some embodiments, the non-reducing end glycan residual compound is
a monosaccharide. In some embodiments, the non-reducing end glycan
residual compound is not a monosaccharide.
[0033] In some embodiments, the second biomarker is derived or
generated from the reducing end of the same glycan from which the
first non-reducing end glycan residual compound biomarker was
generated. In some embodiments, the second biomarker is derived or
generated from the internal oligosaccharide structures of the same
glycan from which the first non-reducing end glycan residual
compound biomarker was generated. In some embodiments, the disease
or disorder is caused by the abnormal function of a glycan
degradation enzyme in the individual, and wherein the second
biomarker can be generated by treating the first non-reducing end
glycan residual compound biomarker with the glycan degradation
enzyme that is functioning abnormally in the individual.
[0034] In some embodiments, the disease or condition associated
with abnormal glycan biosynthesis, degradation, or accumulation is
a lysosomal storage disease. In some embodiments, the lysosomal
storage disease is Mucopolysaccharidosis. In some embodiments, the
Mucopolysaccharidosis is MPS I, II, IIIA, IIIB, IIIC, IIID, IVA,
IVB, VI, or VII. In some embodiments, the disease or condition
associated with abnormal glycan biosynthesis, degradation, or
accumulation is Metachromatic Leukodystrophy or Krabbe disease. In
some embodiments, the disease or condition associated with abnormal
glycan biosynthesis, degradation, or accumulation is
Gangliosidosis. In some embodiments, the Gangliosidosis is Tay
Sachs, Sandhoff, AB Variant, or GM-1 Gangliosidoses.
[0035] In some embodiments, the presence of and/or measure of the
first non-reducing end glycan residual compound biomarker in
combination with or in relation to the second biomarker is utilized
to monitor the treatment of a disorder associated with the abnormal
biosynthesis of glycans. In some embodiments, the presence of
and/or measure of the first non-reducing end glycan residual
compound biomarker in combination with or in relation to the second
biomarker is utilized to monitor the treatment of a disorder
associated with the abnormal degradation or accumulation of
glycans. In some embodiments, the treatment is enzyme replacement
therapy. In some embodiments, the absence of an increase in the
second biomarker combined with a reduction in the non-reducing end
glycan residual compound biomarker indicates a positive response to
treatment of the disorder associated with abnormal degradation or
accumulation of glycans.
[0036] In some instances, a method described herein comprises
utilization of a first biomarker that is a non-reducing end glycan
biomarker, e.g., as set forth in US 2010/0184013, which is
incorporated by reference herein in its entirety. In certain
embodiments, the first biomarker is a C4-C5 non-reducing end
saturated oligosaccharide. In some embodiments, the non-reducing
end residue of the first biomarker (e.g., one or more disaccharide
and/or one or more trisaccharide) are free of carbon-carbon
unsaturation.
[0037] In some embodiments, the abnormal glycan accumulation or
disorder associated therewith is caused by an abnormally
functioning glycan degradation enzyme and wherein the abnormally
functioning glycan degradation enzyme and glycan degradation enzyme
are of the same type (e.g., the glycan degradation utilized in the
transformation process is a functioning glycan degradation enzyme
whereas the abnormally functioning enzyme is not, such as due to
deletions, insertions, substitutions, or other modifications to the
enzyme sequence). In certain embodiments, the abnormally
functioning glycan degradation enzyme functions abnormally as a
result of being present in an abnormally low amount, functioning
improperly, or a combination thereof. In some embodiments, the
abnormal glycan accumulation comprises the accumulation of abnormal
amounts of glycans. In certain embodiments, the abnormal glycan
accumulation comprises the accumulation of abnormal amounts of
normal glycans. In some embodiments, the abnormal glycan
accumulation comprises the accumulation of abnormal amounts of
abnormal glycans.
[0038] In certain embodiments, the biomarker is not present in the
original biological sample. In some embodiments, the biomarker is
not present in the biological sample after isolating a population
of glycans therefrom (e.g., prior to transformation of the glycan
according to a process described herein).
[0039] In certain embodiments, the normally functioning glycan
degradation enzyme is a glycosidase, sulfatase, phosphorylase,
deacetylase or a combination thereof. In some embodiments, the
normally functioning glycan degradation enzyme is a glycosidase
selected from an exo-glycosidase and an endo-glycosidase. In
certain embodiments, the glycosidase is an exo-glycosidase selected
from the group consisting of a galactosidase, and a glucuronidase.
In some embodiments, the generated biomarker is a glycan residual
compound. In some embodiments, the glycan residual compound is a
monosaccharide. In certain embodiments, the glycan residual
compound is sulfate, phosphate, acetate, or a combination thereof.
In certain embodiments, the glycan residual compound has a
molecular weight of less than 2000 g/mol, less than 1500 g/mol,
less than 1000 g/mol, less than 500 g/mol, less than 400 g/mol,
less than 300 g/mol, less than 260 g/mol, less than 200 g/mol, less
than 100 g/mol, or the like (e.g., prior to tagging with any
detectable label that may be included in a process described
herein).
[0040] In some embodiments, any process described herein further
comprises purifying a biological sample prior to transforming a
glycan thereof. In some embodiments, the process of purifying a
biological sample comprises removing monosaccharides therefrom,
removing sulfates therefrom, removing phosphates therefrom,
removing acetate therefrom, or a combination thereof.
[0041] In certain embodiments, transforming a glycan of a
biological sample with a normally functioning glycan degradation
enzyme comprises transforming a glycan of a biological sample with
a plurality of normally functioning glycan degradation enzymes. In
some embodiments, the glycan is treated with a plurality of
normally functioning glycan degradation enzymes concurrently,
sequentially, or a combination thereof.
[0042] In specific embodiments, a disorder associated with an
abnormal glycan accumulation is any disorder described in Tables
1-4 (e.g., MPS I) and the normally functioning glycan degradation
enzyme is any enzyme described in Tables 1-4 (e.g.,
L-iduronidase).
[0043] In some embodiments, determining whether the amount of
liberated glycan residue is abnormal comprises labeling the glycan
residue with a detectable label and measuring the amount of labeled
glycan residue with an analytical instrument. In certain
embodiments, the detectable label is a mass label, a radioisotope
label, a fluorescent label, a chromophore label, or affinity label.
In some embodiments, the amount of liberated glycan is measured
using UV-V is spectroscopy, IR spectroscopy, mass spectrometry, or
a combination thereof.
[0044] Provided in some embodiments herein is a method of
monitoring the treatment of a disorder associated with the abnormal
degradation, biosynthesis and/or accumulation of glycans, the
methods comprising: [0045] a. following administration of an agent
for treating a disorder associated with the abnormal degradation,
biosynthesis and/or accumulation of glycans to an individual in
need thereof, using an analytical instrument to measure the amount
of a population of a non-reducing end glycan residual compounds
present in a transformed biological sample that has been prepared
by: [0046] treating a population of glycans, in or isolated from a
biological sample taken from the individual, with at least one
normally functioning glycan degradation enzyme to liberate
non-reducing end glycan residual compound; [0047] b. determining
whether or not the amount of liberated non-reducing end glycan
residue has decreased or increased at a slower rate compared to the
amount or rate of increase prior to administration of the agent for
treating a disorder associated with the abnormal degradation,
biosynthesis and/or accumulation of glycans.
[0048] In some embodiments, the disorder associated with the
abnormal degradation, biosynthesis and/or accumulation of glycans
is a lysosomal storage disease, a cancerous disease, or an
infectious disease. In certain embodiments, the normally
functioning glycan degradation enzyme is a glycosidase, sulfatase,
phosphorylase, deacetylase, or a combination thereof. In some
embodiments, the normally functioning glycan degradation enzyme is
a glycosidase selected from an exo-glycosidase and an
endo-glycosidase. In certain embodiments, the glycan residual
compound is a monosaccharide, sulfate, phosphate, acetate, or a
combination thereof. In some embodiments, transforming a glycan of
a biological sample with a normally functioning glycan degradation
enzyme comprises transforming a glycan of a biological sample with
a plurality of normally functioning glycan degradation enzymes. In
certain embodiments, the glycan is treated with a plurality of
normally functioning glycan degradation enzymes concurrently,
sequentially, or a combination thereof.
[0049] In some embodiments, prior to measuring the amount of a
population of non-reducing end glycan residual compounds, the
non-reducing end glycan residual compounds are labeled with a
detectable label. In certain embodiments, the detectable label is a
mass label, a radioisotope label, a fluorescent label, a
chromophore label, or affinity label. In some embodiments, the
amount of liberated glycan is measured using UV-Vis spectroscopy,
IR spectroscopy, mass spectrometry, or a combination thereof.
BRIEF DESCRIPTION OF THE DRAWINGS
[0050] The novel features of the invention are set forth with
particularity in the appended claims. A better understanding of the
features and advantages of the present invention will be obtained
by reference to the following detailed description that sets forth
illustrative embodiments, in which the principles of the invention
are utilized, and the accompanying drawings of which:
[0051] FIG. 1 illustrates compounds present in a normal biological
sample not subject to an enzymatic glycan residual liberation
process described herein.
[0052] FIG. 2 illustrates compounds present in a normal biological
subject to an enzymatic glycan residual liberation process
described herein.
[0053] FIG. 3 illustrates compounds present in a biological sample
of an individual suffering from a disorder associated with abnormal
glycan accumulation not subject to an enzymatic glycan residual
liberation process described herein.
[0054] FIG. 4 illustrates compounds present in a biological sample
of an individual suffering from a disorder associated with abnormal
glycan accumulation subject to an enzymatic glycan residual
liberation process described herein.
[0055] FIG. 5 illustrates a scheme for determining non-reducing
ends and internal disaccharide. Eliminative depolymerization of a
heparan sulfate oligosaccharide with heparan lyase results in the
release of internal disaccharide residues (dashed arrows) that
contain an unsaturated uronic acid moiety (dotted circles). Because
of its terminal location, the non-reducing end liberated from the
left end of the chain as drawn lacks the .DELTA.4,5-double bond and
is 18 amu larger than a corresponding internal disaccharide.
Reductive amination with aniline ([12C.sub.6]An) facilitates
separation of the various disaccharides by LC/MS, yielding the m/z
values for the molecular ions indicated within the parentheses. The
glycan structures are graphically represented by geometric symbols,
which are defined in the lower part of the FIG. 43. To simplify the
representation of constituent oligosaccharides from
glycosaminoglycans, we use a Disaccharide Structure Code (DSC)15.
In DSC, a uronic acid is designated as U, G, I, or D for an
unspecified hexuronic acid, D-glucuronic acid, L-iduronic acid, or
.DELTA.4,5-unsaturated uronic acid, respectively. The hexosamines
are designated in upper case for glucosamine and lower case for
galactosamine, and the N-substituent is either H, A, S or R for
hydrogen, acetate, sulfate, or some other substituent,
respectively. The presence and location of ester linked sulfate
groups are depicted by the number of the carbon atom on which the
sulfate group is located or by 0 if absent. For example, I2S6
refers to a disaccharide composed of 2-sulfoiduronic
acid-N-sulfoglucosamine-6-sulfate, whereas D2S6 refers to same
disaccharide, but bearing a .DELTA.4,5-double bond in the uronic
acid.
[0056] FIG. 6 illustrates MPS Non-reducing end carbohydrates. The
defective enzyme for each MPS subclass is displayed along with the
liberated NRE carbohydrates characteristic of MPS I, II, IIIA,
IIIB, IIIC, IIID, VI and VII using geometric symbols. The matrices
show all NRE carbohydrates that are theoretically possible for each
MPS subclass using the DSC. The boxes with a black background and
whiteface font depict structures that were detected and whose
identities were confirmed by their co-chromatography and identical
mass spectra as standards, as well as their sensitivity to
exoglycosidases or propionic acid anhydride. Suspected structures
shown in boxes with a gray background are implied from the liquid
chromatography/mass spectra data, i.e. their size and content of
sulfate and acetate groups are consistent with the proposed
structures. The structures in boxes with a white background are
theoretically possible, but have not been observed. The m/z values
for both the free molecular ions and adduction ions formed with the
ion pairing reagent dibutylamine (DBA) are listed. The single
letter designations for the variously modified sugars are described
in FIG. 5. The glycan structures are graphically represented by
geometric symbols, which are defined in the lower part of the
figure
[0057] FIG. 7 illustrates analysis of non-reducing ends found in
MPS I and Sanfilippo heparan sulfate. (a) Depolymerized heparan
sulfate from MPS I fibroblasts (GM01391) was tagged with
[12C6]aniline and mixed with standard [13C6]aniline-labeled
unsaturated disaccharides and I0S0. The sample was analyzed by
LC/MS and the extracted ion current for all known NRE and internal
disaccharides was recorded: peak 1, D0A0; peak 2, D0S0; peak 3,
D0A6; peak 4, D0S6; peak 5, D2A0; peak 6, D2S0; and peak 7, D2S6.
The asterisk marks the [12C6]aniline tagged NRE, which comigrated
with [13C6]aniline-labeled I0S0 standard (inset). (b) Mass spectrum
for the I0S0 peak shown in panel A. GAGs purified from (c) MPS IIIA
(GM00643), (d) MPS IIIB (GM01426), (e) MPS IIIC (GM05157) and (f)
MPS IIID (GM17495) fibroblasts were subjected to NRE analysis. For
simplicity, only the extracted ion current for m/z values
corresponding to monosaccharide and trisaccharide (dp3) NREs are
shown for each sample. When the NRE structure was identified by
comparison with commercially available standards, the name is
indicated in DSC and glycan symbols. The dp3(0Ac,4S) NRE residues
in the MPS IIIA and the MPS IIIC samples were detected as adduction
ions with the ion pairing reagent ([M-2H+DBA]-1); hence their m/z
values were increased by 129 amu (see FIG. 6). The insets in panels
c and f show the mass spectra for the monosaccharide biomarkers S0
and H6, respectively, and the corresponding [13C6]aniline tagged
standards (arrows in panels c and f).
[0058] FIG. 8 illustrates systematic diagnostic screening of GAG
samples for various MPS disorders. Shown is a flow chart for MPS
discovery based on the detection of diagnostic non-reducing end
glycans present in GAG samples extracted from patient or animal
model sources. The detection criteria are based on NRE size
(monosaccharide, disaccharide and trisaccharide), m/z value, and
structural features (number of acetates (Ac) or sulfates (S)). For
a complete unknown, portions of the sample are analyzed in parallel
for heparan sulfate and chondroitin/dermatan sulfate NREs.
[0059] FIG. 9 illustrates a comparison of total heparan sulfate to
N-sulfoglucosamine (S0) in MPS IIIA samples. (a) Heparan sulfate
from normal (black bars) and MPS IIIA (light grey bars) urine was
analyzed. The individual disaccharides and NRE N-sulfoglucosamine
(S0) was quantitated relative to standards. Since trisaccharide
standards are not available, the values of the extracted ion
current for S0U2S0 are shown. (b) Analysis of normal (black bars)
and MPS IIIA (light grey bars) brain heparan sulfate as in panel A.
(c) MPS IIIA cells underwent enzyme replacement by incubation with
0.06 mU/ml of sulfamidase for 48 hours prior to GAG extraction and
subsequent analysis. The amount of heparan sulfate (black bars),
the monosaccharide biomarker S0 (light grey bars), and the
trisaccharide biomarker S0U2S0 (dark grey bars) were measured and
compared to samples from cells without enzyme supplementation. The
bars represent the average.+-.standard deviation, n=3.
[0060] FIG. 10 illustrates a structural comparison of MPS I NRE
biomarker with I0S0 standard. Tandem mass spectrometry was carried
out on [.sup.13C.sub.6]aniline-tagged I0S0 standard. The
predominant daughter ions and their assignments based on m/z values
are indicated in the mass spectrum (a). A schematic representation
of the primary inter-ring cleavage of I0S0 is also shown. The m/z
values are shown next to each fragment ion. After labeling with
[.sup.12C.sub.6]aniline, the putative I0S0 NRE found in heparan
sulfate from cultured fibroblasts from a MPS I patient (GM01391)
was also subjected to tandem mass spectrometry (b). The m/z values
shown in each CID spectrum are consistent with the difference in
mass between [.sup.13C.sub.6]aniline and [.sup.12C.sub.6]aniline.
Identity between the standard and the MPS I NRE is indicated by the
similar CID spectra.
[0061] FIG. 11 illustrates analysis of non-reducing end structures
found in MPS I, MPS II and MPS VII. GAG samples purified from (a,d)
MPS I (GM01391), (b,e) MPS II (GM00615) and (c,f) MPS VII (GM02784)
fibroblasts were subjected to enzymatic depolymerization with
heparan lyase (a,b,c) or chondroitinase ABC (d,e,f) followed by
GRIL-LC/MS analysis. The accumulative extracted ion current for m/z
values corresponding to heparan sulfate and chondroitin/dermatan
sulfate NRE structures detected in each sample is shown. In the
absence of authentic standards, the relative abundance of the
individual biomarkers cannot be derived from these spectra due to
differences in ionization efficiencies. The identification of the
uronic acids is based on chromatographic separation of isobaric
species (e.g. G0S0 and G0S6 resolve from I0S0 and I0S6,
respectively), differential sensitivity to .alpha.-L-iduronidase,
and inference based on the nature of the enzyme deficiency in the
cells. Putative structures are indicated by both DSC and glycan
symbols as well as their m/z values. In cases where two isobaric
species could not be discriminated by CID analysis (I0a4/I0a6 in
panel d and I2a4/I2a6 in panel e), both species are shown.
[0062] FIG. 12 illustrates removal of the non-reducing end
biomarker in MPS I by .alpha.-iduronidase treatment. An equal
amount of heparan sulfate isolated from fibroblasts of a patient
with MPS I (GM01391) was treated with recombinant
.alpha.-iduronidase or with BSA. The samples were then tagged with
[.sup.12C.sub.6] aniline, mixed with 10 pmole of
[.sup.13C.sub.6]aniline-labeled I0S0 standard, and analyzed by
GRIL-LC/MS. The mass spectrum for the BSA-treated samples shows the
MPS I NRE and the I0S0 standard (a). The mass spectrum of the
iduronidase-treated sample shows the loss of the MPS I biomarker
(b). The m/z values for all species detected are indicated above
the major peaks.
[0063] FIG. 13 illustrates removal of the non-reducing end
biomarker found in MPS II by Iduronate-2-sulfatase. Equal amounts
of heparan sulfate isolated from fibroblasts from an MPS II patient
(GM00615) were treated with either BSA or recombinant
iduronate-2-sulfatase prior to NRE analysis. The accumulative
extracted ion current for m/z values corresponding to 2-O-sulfated
and non-2-O-sulfated NRE species for the BSA-treated sample (black
trace) and the iduronate-2-sulfatase-treated sample (red trace) are
shown in the chromatogram. The NRE structures consistent with the
m/z values for the species detected after each treatment are
shown.
[0064] FIG. 14 illustrates GRIL-LC/MS analysis of MPS VI
chondroitin sulfate NRE. GAG purified from MPS VI (GM00519)
fibroblasts was enzymatically depolymerized with chondroitinase ABC
followed by GRIL-LC/MS analysis. The accumulative extracted ion
current for m/z values corresponding to NRE monosaccharide
structures GaINAc6S (a6) and GaINAc4S (a4) standards labeled with
[.sup.13C.sub.6] aniline are shown (bottom red trace) and the
endogenous a4 labeled with [.sup.12C.sub.6] aniline detected in the
MPS VI sample is shown (top black trace). The mass spectrum are
indicated for the a4 peak in the top trace is shown in the inset
with the m/z values for the isotopic clusters for the endogenous
[.sup.12C.sub.6]aniline-tagged a4 (m/z=377.11) and the
[.sup.13C.sub.6]aniline-labeled a4 standard (m/z=383.13).
[0065] FIG. 15 illustrates removal of the non-reducing end
biomarker in MPS IIIA by sulfamidase. Heparan sulfate purified from
fibroblasts from two MPS IIIA patients (GM00643 and GM00934) was
treated with either BSA (black bars) or sulfamidase (light grey
bars) prior to GRIL-LC/MS analysis. [.sup.13C.sub.6]aniline-labeled
S0 standard (10 pmol) was added to each sample and used to
calculate the recovery of S0.
[0066] FIG. 16 illustrates CID analysis of NRE trisaccharides found
in Sanfilippo sub-classes. Representative trisaccharide NRE
structures detected in heparan sulfate from fibroblasts of MPS
IIIA, MPS IIIB and MPS IIIC patients were subjected to collision
induced dissociation. The most likely structures are indicated
along with the product ions detected. The structural parameters for
each parent ion are displayed below each structure. To confirm the
presence of an unsubstituted glucosamine residue in the MPS IIIC
trisaccharides, aniline-labeled samples were acylated with
propionic anhydride (PA), which reacts with both primary and
secondary amines. The solid arrows point out primary and secondary
amines susceptible to acylation by propionic anhydride. All of the
MPS IIIC trisaccharides gained mass consistent with the addition of
two propionyl groups. In contrast, the MPS IIIA and IIB
trisaccharides picked up a single propionyl group due to
proprionylation at the bridging secondary amine derived from
reductive amination with aniline. Thus, the addition of a second
proprionate group to MPS IIIC trisaccharides is consistent with
their containing an unsubstituted glucosamine unit. Due to the
detection of only two product ions for the MPS IIIC NRE
trisaccharide, two potential structures are possible.
DETAILED DESCRIPTION OF THE INVENTION
[0067] While preferred embodiments of the present invention have
been shown and described herein, such embodiments are provided by
way of example only. Numerous variations, changes, and
substitutions will now occur to those skilled in the art without
departing from the invention. It should be understood that various
alternatives to the embodiments of the invention described herein
may be employed in practicing the invention. It is intended that
the following claims define the scope of the invention and that
methods and structures within the scope of these claims and their
equivalents be covered thereby.
[0068] Glycosaminoglycans comprise a reducing end and a
non-reducing end. Normal biological processes degrade
glycosaminoglycans (such as heparan sulfate which has a normal
component of about 50-80 kDa) into monosaccharides. Disorders
associated with abnormal glycosaminoglycan degradation,
biosynthesis, and/or accumulation can result in an accumulation of
glycosaminoglycans and fragments thereof.
[0069] Many human diseases are caused by or correlated with changes
in glycosaminoglycans. In order to use these changes as biomarkers
of disease, analytical methods are used to quantify the changes.
Some methods use antibodies, chromatography and/or mass
spectrometry techniques to resolve and quantify the intact or
partially intact glycans. The use of such methods are challenging
due to the complexity and number of possible glycan structures
present in biological samples. To address the complexity, methods
have been developed which employ glycan digesting enzymes to
liberate and quantify homogenous oligosaccharides generated from
the polymeric glycosaminoglycans. The use of individual
oligosaccharides as the biomarker of disease may not be sufficient.
As a result, an opportunity exists to combine oligosaccharide
biomarkers to provide the necessary insight related to presence of
disease, prediction of severity, and characterization of the
response to treatment.
[0070] Provided herein is a method of detecting abnormal glycan
accumulation, e.g., in human disease. In some instances, the
process described herein includes a strategy to quantify the
changes by measuring the abundance of all glycans with a disease
related glycan residual compound on the non-reducing end of glycans
from a biological sample (e.g., monosaccharides and/or their
modifications such as sulfation, acetylation, phosphorylation, or
the like).
[0071] Provided in certain embodiments herein are methods of
detecting glycan accumulation in a biological sample, the method
comprising: [0072] a. transforming a glycan of a biological sample
with a normally functioning glycan degradation enzyme to liberate a
glycan residual compound from the non-reducing end of the glycan;
[0073] b. measuring the amount of the glycan residual compound
liberated by the functioning glycan degradation enzyme with an
analytical device.
[0074] In certain embodiments, the method is associated with
diagnosing an individual with abnormal glycan accumulation, or a
disorder associated therewith.
[0075] Therefore, in specific embodiments, provided herein is a
method of diagnosing an individual as having an abnormal glycan
accumulation or a disorder associated with an abnormal glycan
accumulation, the method comprising: [0076] a. transforming a
glycan of a biological sample with a normally functioning glycan
degradation enzyme to liberate a glycan residual compound from the
non-reducing end of the glycan; [0077] b. measuring the amount of
the glycan residual compound liberated by the functioning glycan
degradation enzyme with an analytical device; and [0078] c.
determining whether the amount of liberated glycan residue is
abnormal.
[0079] In certain instances, methods of detecting abnormal glycan
accumulation works based on the observation that altered glycans
generated in a disease state are caused by an alteration in the
activity of a biosynthetic enzyme (e.g., via increased expression,
increased activity, increased substrate, or the like) that leads to
the production of thousands of unique structures.
[0080] For example, in certain instances, the induction of an alpha
2,3 sialyltransferase leads to the novel expression of thousands of
different glycans (potentially from multiple glycan classes) that
present a non-reducing terminal alpha 2,3 linked sialic acid. By
quantifying a limited set of these novel structures using current
methods, only a fraction of the disease related structures are
measured. Instead, as provided in certain embodiments herein, if a
sample containing glycans (crude or purified for a specific glycan
class) is treated with an alpha 2,3 sialidase to liberate the
non-reducing end sialic acid, the free sialic acid (non-reducing
end glycan residual) can be measured. This signal would represent a
larger portion of the thousands of altered glycan structures that
are made in the disease state due to the altered expression of the
alpha 2,3 sialyltransferase. Furthermore, in certain embodiments,
depending on the signal (i.e., measurement) of the sialic acid
liberated, a determination is made as to whether or not the
accumulation of sialic acid is abnormal and/or whether or not such
levels of accumulated sialic acid is associated with a
disorder.
[0081] Another example of the process includes a method involving a
biological sample containing glycans (purified or not) that is
treated with an exo-glycosidase (for example a
.beta.-galactosidase). In some of such embodiments, enzymatic
treatment cleaves non-reducing end monosaccharides within the
chosen enzymes specificity (e.g., .beta.-linked galactose residues)
and liberates them as free monosaccharide (e.g., galactose). In
various embodiments, the free monosaccharide is isolated and
quantified by any analytical method (HPLC, MS, GC, etc), and any
disease that presents changes in the levels of non-reducing end
.beta.-linked galactose residues is detected or diagnosed.
[0082] Similar methods are also optionally utilized in methods of
monitoring and/or determining the therapeutic of a treatment or
treatment regimen, particularly in the treatment of a disorder
associated with abnormal glycan accumulation. For example, provided
in certain embodiments herein is a method of monitoring the
treatment of disorders associated with the abnormal degradation,
biosynthesis and/or accumulation of glycans, the methods
comprising: [0083] a. following administration of an agent for
treating a disorder associated with the abnormal degradation,
biosynthesis and/or accumulation of glycans to an individual in
need thereof, using an analytical instrument to measure the amount
of a population of a non-reducing end glycan residue present in a
transformed biological sample that has been prepared by: [0084]
treating a population of glycans, in or isolated from a biological
sample taken from the individual, with at least one normally
functioning glycan degradation enzyme to liberate non-reducing end
glycan residue; [0085] b. determining whether or not the amount of
liberated non-reducing end glycan residue has decreased or
increased at a slower rate compared to the amount or rate of
increase prior to administration of the agent for treating a
disorder associated with the abnormal degradation, biosynthesis
and/or accumulation of glycans.
[0086] In some embodiments, any process described herein comprises:
[0087] a. comparing an amount of a population of one or more glycan
residual compound present in a transformed biological sample to an
amount of a population of one or more glycan residual compound
present in a control biological sample that has been treated in a
manner substantially similar to the transformed biological
sample.
[0088] In certain embodiments, a control biological sample utilized
in any process described herein was provided from an individual
that does not suffer from a disorder being diagnosed. In other
embodiments, a control biological sample is taken from an
individual suffering from a disorder being diagnosed. In certain
embodiments, the result obtained from the control biological sample
is stored in a database. In such cases a test sample is optionally
compared to a plurality of control data in a database. Moreover in
certain embodiments, any diagnostic process described herein is
optionally utilized alone or in combination with other diagnostic
techniques. Other diagnostic techniques include, by way of
non-limiting example, symptom analysis, biopsies, detection of
accumulation of other compounds in biological samples, or the like.
In some embodiments, control biological samples are optionally
taken from the same individual at substantially the same time,
simply from a different location (e.g., one inflamed/arthritic
synovial joint fluid vs the contralateral non-arthritic synovial
joint). In other embodiments, control biological samples are
optionally taken from the same individual at different points in
time (e.g., before therapy and after therapy if the method being
utilized is a method of monitoring a treatment therapy).
[0089] In some embodiments, provided herein is a method of
monitoring the treatment of a disorder associated with the abnormal
degradation, biosynthesis and/or accumulation of glycans, the
method comprising: [0090] a. following administration of an agent
for treating a disorder associated with the abnormal degradation,
biosynthesis and/or accumulation of glycans to an individual in
need thereof, using an analytical instrument to measure the amount
of a population of a biomarker comprising a non-reducing end glycan
residual compounds present in a transformed biological sample, the
biomarker being generated by treating a population of glycans, in
or isolated from a biological sample from the individual, with at
least one digesting glycan enzyme(s), wherein prior to enzyme
treatment, the biomarker is not present in abundance in samples
from individuals with the disease or condition relative to
individuals without the disease or condition, and [0091] b.
determining whether or not the amount of biomarker has decreased or
increased at a slower rate compared to the amount or rate of
increase prior to administration of the agent for treating a
disorder associated with the abnormal degradation, biosynthesis
and/or accumulation of glycans.
[0092] In some embodiments, the disorder associated with the
abnormal degradation, biosynthesis and/or accumulation of glycans
is a lysosomal storage disease, a cancerous disease, an
inflammatory disease, an infectious disease, a central nervous
system disease, or a cardiovascular disease.
[0093] In some embodiments, the normally functioning glycan
degradation enzyme is a glycosidase, sulfatase, phosphorylase,
deacetylase, or a combination thereof. In some embodiments, the
normally functioning glycan degradation enzyme is a glycosidase is
selected from an exo-glycosidase and an endo-glycosidase. In some
embodiments, the glycan residual compound is a monosaccharide,
sulfate, phosphate, acetate, or a combination thereof. In some
embodiments, transforming a glycan of a biological sample with a
normally functioning glycan degradation enzyme comprises
transforming a glycan of a biological sample with a plurality of
normally functioning glycan degradation enzymes. In some
embodiments, the glycan is treated with a plurality of normally
functioning glycan degradation enzymes concurrently, sequentially,
or a combination thereof.
[0094] In some embodiments, prior to measuring the amount of a
population of non-reducing end glycan residual compounds, the
non-reducing end glycan residual compounds are labeled with a
detectable label. In some embodiments, the detectable label is a
mass label, a radioisotope label, a fluorescent label, a
chromophore label, or affinity label. In some embodiments, the
amount of liberated glycan is measured using UV-Vis spectroscopy,
IR spectroscopy, mass spectrometry, or a combination thereof.
[0095] Provided in certain embodiments herein are: [0096] a.
Methods using a non-reducing end (NRE) glycan biomarker along with
at least one other glycan biomarkers (e.g., a non-reducing end
glycan biomarker, a reducing end biomarker, and/or an internal
glycan biomarker). In some instances, the use of the two biomarkers
provides a very valuable tool that provides detailed information
about disease severity and/or the response to therapy. In various
aspects, the biomarkers detected and/or analyzed according to the
processed described herein are compared in any suitable manner,
e.g., in a ratio or simultaneous comparison. [0097] b. Methods
using at least two different glycan biomarkers (e.g., wherein each
biomarker is individually selected from a non-reducing end glycan
biomarker, a reducing end biomarker, and an internal glycan
biomarker) to identifying or diagnosing diseases caused by
deficiencies in the accumulation and/or biosynthesis of
glycosaminoglycans. In certain aspects, such methods comprise
comparing the amounts of such biomarkers to each other. In specific
embodiments, the comparison involves determining ratios of the
biomarkers, wherein the biomarkers are glycan fragments generated
by glycosaminoglycan lyase digestion.
[0098] Provided in certain embodiments herein is a method of
diagnosing an individual as having a disease or condition
associated with abnormal glycan biosynthesis, degradation, or
accumulation, the method comprising: [0099] a. generating a
biomarker comprising of one or more non-reducing end glycan
residual compound, wherein the biomarker is generated by treating a
population of glycans, in or isolated from a biological sample from
the individual, with at least one digesting glycan enzymes, wherein
prior to enzyme treatment, the biomarker is not present in
abundance in samples from individuals with the disease or condition
relative to individuals without the disease or condition, and
[0100] b. using an analytical instrument to detect the presence of
and/or measure the amount of the biomarker produced and displaying
or recording the presence of or a measure of a population of the
biomarker; wherein the presence of and/or measure the amount of the
biomarker is utilized to determine the presence, identity, and/or
severity of the disease or condition.
[0101] In some embodiments, the disease or disorder is caused by an
abnormally functioning glycan degradation enzyme and wherein the
abnormally functioning glycan degradation enzyme and the normally
functioning glycan degradation enzyme are of the same type. In some
embodiments, the abnormally functioning glycan degradation enzyme
functions abnormally as a result of being present in an abnormally
low amount, functioning improperly, or a combination thereof. In
some embodiments, the abnormal glycan accumulation comprises the
accumulation of abnormal amounts of glycans. In some embodiments,
the abnormal glycan accumulation comprises the accumulation of
abnormal amounts of normal glycans. In some embodiments, the
abnormal glycan accumulation comprises the accumulation of abnormal
amounts of abnormal glycans.
[0102] In some embodiments, the normally functioning glycan
degradation enzyme is a glycosidase, sulfatase, phosphorylase,
deacetylase, or a combination thereof. In some embodiments, the
normally functioning glycan degradation enzyme is a glycosidase
selected from an exo-glycosidase and an endo-glycosidase. In some
embodiments, the glycosidase is an exo-glycosidase selected from
the group consisting of a galactosidase, and a glucuronidase. In
some embodiments, the glycan residual compound is a monosaccharide.
In some embodiments, the glycan residual compound is sulfate,
phosphate, acetate, or a combination thereof.
[0103] In some embodiments, a biological sample is purified prior
to transforming a glycan thereof. In some embodiments, the process
of purifying a biological sample comprises removing monosaccharides
therefrom, removing sulfates therefrom, removing phosphates
therefrom, removing acetate therefrom, or a combination thereof. In
some embodiments, transforming a glycan of a biological sample with
a normally functioning glycan degradation enzyme comprises
transforming a glycan of a biological sample with a plurality of
normally functioning glycan degradation enzymes. In some
embodiments, the glycan is treated with a plurality of normally
functioning glycan degradation enzymes concurrently, sequentially,
or a combination thereof.
[0104] In some embodiments, the disorder associated with an
abnormal glycan accumulation is MPS I, MPS II, MPS IIIA, MPS IVA,
MPSVI, or Fabry Disease.
[0105] In some embodiments, determining whether the amount of
liberated glycan residue is abnormal comprises labeling the glycan
residue with a detectable label and measuring the amount of labeled
glycan residue with an analytical instrument. In some embodiments,
the detectable label is a mass label, a radioisotope label, a
fluorescent label, a chromophore label, or affinity label. In some
embodiments, the amount of liberated glycan is measured using
UV-Vis spectroscopy, IR spectroscopy, mass spectrometry, or a
combination thereof.
[0106] Provided herein, in certain embodiments, is a method of
diagnosing an individual as having a disease or condition (e.g.,
associated with abnormal glycan biosynthesis, degradation, or
accumulation), the method comprising: [0107] a. generating a first
biomarker comprising a glycan residual compound, wherein the first
biomarker is generated by treating a population of glycans, in or
isolated from a biological sample from the individual, with at
least one digesting glycan enzyme, wherein prior to enzyme
treatment, the first biomarker is not present in abundance in
samples from individuals with the disease or condition relative to
individuals without the disease or condition, [0108] b. generating
a second biomarker comprising a glycan residual compound, wherein
the second biomarker is generated by treating a population of
glycans, in or isolated from a biological sample from the
individual, with at least one digesting glycan enzyme in the same
or different digestion step as provided in step (a), wherein prior
to enzyme treatment, the second biomarker is not present in
abundance in samples from individuals with the disease or condition
relative to individuals without the disease or condition, [0109] c.
using an analytical instrument to detect the presence of and/or
measure the amount of the first and second biomarker produced and
displaying or recording the presence of or a measure of a
population of the first and second biomarkers, and [0110] d.
monitoring and/or comparing the amounts of the first and second
biomarkers in a biological sample; wherein the presence of and/or
measure of the amounts of the first and second biomarkers are
utilized to determine the presence, identity, and/or severity of
the disease or condition.
[0111] In some embodiments, the first biomarker is a non-reducing
end glycan residual compound. In some embodiments, the disease or
disorder is caused by an abnormally functioning glycan degradation
enzyme and wherein the abnormally functioning glycan degradation
enzyme and the digesting glycan enzyme are of the same type. In
some embodiments, the non-reducing end glycan residual compound is
a monosaccharide. In some embodiments, the non-reducing end glycan
residual compound is not a monosaccharide.
[0112] In some embodiments, the second biomarker is derived or
generated from the reducing end of the same glycan from which the
first non-reducing end glycan residual compound biomarker was
generated. In some embodiments, the second biomarker is derived or
generated from the internal oligosaccharide structures of the same
glycan from which the first non-reducing end glycan residual
compound biomarker was generated. In some embodiments, the disease
or disorder is caused by the abnormal function of a glycan
degradation enzyme in the individual, and wherein the second
biomarker can be generated by treating the first non-reducing end
glycan residual compound biomarker with the glycan degradation
enzyme that is functioning abnormally in the individual.
[0113] In some embodiments, the disease or condition associated
with abnormal glycan biosynthesis, degradation, or accumulation is
a lysosomal storage disease. In some embodiments, the lysosomal
storage disease is Mucopolysaccharidosis. In some embodiments, the
Mucopolysaccharidosis is MPS I, II, IIIA, IIIB, IIIC, IIID, IVA,
IVB, VI, or VII. In some embodiments, the disease or condition
associated with abnormal glycan biosynthesis, degradation, or
accumulation is Metachromatic Leukodystrophy or Krabbe disease. In
some embodiments, the disease or condition associated with abnormal
glycan biosynthesis, degradation, or accumulation is
Gangliosidosis. In some embodiments, the Gangliosidosis is Tay
Sachs, Sandhoff, AB Variant, or GM-1 Gangliosidoses.
[0114] In some embodiments, the presence of and/or measure of the
first non-reducing end glycan residual compound biomarker in
combination with or in relation to the second biomarker is utilized
to monitor the treatment of a disorder associated with the abnormal
biosynthesis of glycans. In some embodiments, the presence of
and/or measure of the first non-reducing end glycan residual
compound biomarker in combination with or in relation to the second
biomarker is utilized to monitor the treatment of a disorder
associated with the abnormal degradation or accumulation of
glycans. In some embodiments, the treatment is enzyme replacement
therapy. In some embodiments, the absence of an increase in the
second biomarker combined with a reduction in the non-reducing end
glycan residual compound biomarker indicates a positive response to
treatment of the disorder associated with abnormal degradation or
accumulation of glycans.
Glycan Accumulation:
[0115] In various instances, glycan accumulation occurs in a
biological sample as a result natural glycan biosynthetic and/or
degradation processes. In some instances, abnormal glycan
accumulation occurs in a biological sample as a result of a
disorder or disease within an individual from which the biological
sample is obtained.
[0116] In certain embodiments, abnormal glycan accumulation that is
observable by methods described herein is associated with the
accumulation of glycans in a manner that does not normally occur in
individuals who are not in a disease state.
[0117] In some embodiments, such accumulation includes the
accumulation of abnormal glycans. In certain instances, these
abnormal glycans include glycans that are not normally produced in
an individual, or a particular biological sample thereof, in the
absence of a particular disease state. Therefore, in some
embodiments, abnormal glycan accumulation includes the accumulation
of glycans, the glycans being abnormal themselves, especially in
any significant quantity. In other words, such glycans are abnormal
glycans in individuals or particular biological samples thereof
when such individuals are in a non-diseased, normal, or wild type
state.
[0118] In some embodiments, such accumulation includes the abnormal
accumulation of glycans. In some instances, these glycans are
glycans that normally occur in individuals in a non-diseased state,
but at lower or higher levels or are abnormal only due to the
location wherein they are produced. Therefore, in some embodiments,
abnormal glycan accumulation includes the accumulation of abnormal
amounts of glycans or the location thereof, the glycans being
normally occurring or abnormal glycans. In other words, the amount
of glycan accumulation is abnormal in individuals, or particular
biological samples thereof, when such individuals are in a
non-diseased, normal, or wild type state.
Biological Sample:
[0119] Biological samples suitable for analysis according to the
methods and processes described herein include, by way of
non-limiting example, blood, serum, urine, hair, saliva, skin,
tissue, plasma, cerebrospinal fluid (CSF), amniotic fluid, nipple
aspirate, sputum, tears, lung aspirate, semen, feces, synovial
fluid, nails, or the like. In specific embodiments, the biological
samples suitable for analysis according to the methods and
processes described herein include, by way of non-limiting example,
urine, serum, plasma, or CSF. In certain embodiments, processes for
detecting glycan in a sample comprise providing, from the
individual, a test biological sample that comprises glycan. In some
embodiments, providing a test biological sample from an individual
includes obtaining the sample from the individual or obtaining the
sample from another source (e.g., from a technician or institution
that obtained the sample from the individual). In some embodiments,
the biological sample is obtained from any suitable source, e.g.,
any tissue or cell (e.g., urine, serum, plasma, or CSF) of an
individual. In certain embodiments, the tissue and/or cell from
which the glycans are recovered is obtained from liver tissue or
cells, brain tissue or cells, kidney tissue or cells, or the
like.
[0120] In certain embodiments, a biological sample according to any
process described herein is taken from any individual. In some
embodiments, the individual is an individual suspected of suffering
from a disorder associated with abnormal glycan accumulation,
biosynthesis, and/or degradation. In certain embodiments, the
individual is a newborn or fetus.
[0121] In some embodiments, provided herein is a composition
comprising isolated glycans, wherein the glycans were isolated from
a biological sample, and one or more glycan degradation enzyme. In
certain embodiments, the composition further comprises one or more
biomarker generated according to any method described herein (e.g.,
wherein the biomarker is a non-reducing end glycan residual
compound). In certain embodiments, provided herein is a biomarker
described herein (e.g., a labeled or non-labeled non-reducing end
glycan residual compound) and an analytical instrument or
chromatographic resin.
Degradation Enzymes:
[0122] In certain embodiments, any suitable enzyme is optionally
utilized in order to remove a glycan residual compound from the
non-reducing end of a glycan. In certain disorders, e.g., as
described herein, various types of abnormal glycan accumulation
occurs. In certain instances, this type of glycan accumulation is
detected and/or measured utilizing any suitable enzyme, e.g., as
described herein. For example, Tables 1-4 illustrate various
enzymes that are utilized in various embodiments of the processes
described herein. Any enzyme with the desired specificity is
optionally utilized in any process herein (i.e., to liberate the
non-reducing end structures). Enzymes suitable for use in the
processes described herein include, by way of non-limiting example,
eukaryotic, prokaryotic, native, or recombinant enzymes.
[0123] In certain embodiments, a disorder associated with abnormal
glycan accumulation includes a disorder associated therewith is
caused by an abnormally functioning glycan degradation enzyme. In
various embodiments, the abnormally functioning glycan degradation
enzyme functions abnormally as a result of being present in an
abnormally low amount, functioning improperly, or a combination
thereof. For example, an abnormally functioning glycan degradation
enzyme functions abnormally as a result of being present in an
amount of less than 50%, less than 40%, less than 30%, less than
20%, less than 10%, or less than 5% than is present in an
individual with normal amounts of the glycan degradation enzyme
(e.g., an individual in a non-diseased, normal, or wild type
state). In further or alternative embodiments, abnormally
functioning glycan degradation enzymes are present in a normal
amount, but do not function properly in degrading glycans. For
example, such enzymes may be have amino acid substitutions in the
sequences thereof that reduce or eliminate the glycan degradative
properties of the enzyme.
[0124] In some embodiments, wherein abnormal glycan accumulation
results, at least partially from, an abnormally functioning glycan
degradation enzyme, a normally functioning glycan degradation is
optionally utilized, particularly wherein the abnormally
functioning glycan degradation enzyme and the normally functioning
glycan degradation enzyme are of the same type.
[0125] Normally functioning glycan degradation enzymes that are
used in various embodiments described herein include, by way of
non-limiting example, glycosidases, sulfatases, phosphorylases,
deacetylases, sialidases, or combinations thereof. In more specific
embodiments, a normally functioning glycan degradation enzyme is a
glycosidase, e.g., an exo-glycosidase or an endo-glycosidase. In
more specific embodiments, the glycosidase is an exo-glycosidase,
e.g., galactosidase, and a glucuronidase. In some embodiments, such
enzymes serve to remove various glycan residual compounds, such as,
monosaccharides, sulfate, phosphate, acetate, sialic acid, or
combinations thereof, which are detected and/or measured in methods
described herein.
[0126] In certain embodiments, one or normally functioning glycan
degradation enzyme is optionally utilized to liberate a targeted
glycan residual compound. Multiple enzyme treatments of glycans
within a biological sample are useful in various embodiments, e.g.,
wherein a particular enzyme is unable to liberate a targeted
residual glycan compound without first modifying the non-reducing
end of the glycan. For example, a first enzyme is optionally
utilized to remove a sulfate so that a second enzyme can be
utilized to remove a monosaccharide. In various embodiments, the
glycans are treated with a plurality of normally functioning glycan
degradation enzymes concurrently, sequentially, or a combination
thereof.
[0127] Various enzymes that are used in various embodiments of the
methods described herein include, by way of non-limiting example, a
glycosidase. Non-limiting examples of glycosidase that are
optionally utilized in the methods described herein include, by way
of non-limiting example, enzymes categorized as 3.2.1.X by BRENDA
(the comprehensive Enzyme Information System) including 3.2.1.1
alpha-amylase, 3.2.1.B1 extracellular agarase, 3.2.1.2
beta-amylase, 3.2.1.3 glucan 1,4-alpha-glucosidase, 3.2.1.4
cellulase, 3.2.1.5 licheninase, 3.2.1.6 endo-1,3(4)-beta-glucanase,
3.2.1.7 inulinase, 3.2.1.8 endo-1,4-beta-xylanase, 3.2.1.9
amylopectin-1,6-glucosidase, 3.2.1.10 oligo-1,6-glucosidase,
3.2.1.11 dextranase, 3.2.1.12 cycloheptaglucanase, 3.2.1.13
cyclohexaglucanase, 3.2.1.14 chitinase, 3.2.1.15 polygalacturonase,
3.2.1.16 alginase, 3.2.1.17 lysozyme, 3.2.1.18 exo-alpha-sialidase,
3.2.1.19 heparinase, 3.2.1.20 alpha-glucosidase, 3.2.1.21
beta-glucosidase, 3.2.1.22 alpha-galactosidase, 3.2.1.23
beta-galactosidase, 3.2.1.24 alpha-mannosidase, 3.2.1.25
beta-mannosidase, 3.2.1.26 beta-fructofuranosidase, 3.2.1.27
alpha-1,3-glucosidase, 3.2.1.28 alpha,alpha-trehalase, 3.2.1.29
chitobiase, 3.2.1.30 beta-D-acetylglucosaminidase, 3.2.1.31
beta-glucuronidase, 3.2.1.32 xylan endo-1,3-beta-xylosidase,
3.2.1.33 amylo-alpha-1,6-glucosidase, 3.2.1.34 chondroitinase,
3.2.1.35 hyaluronoglucosaminidase, 3.2.1.36 hyaluronoglucuronidase,
3.2.1.37 xylan 1,4-beta-xylosidase, 3.2.1.38 beta-D-fucosidase,
3.2.1.39 glucan endo-1,3-beta-D-glucosidase, 3.2.1.40
alpha-L-rhamnosidase, 3.2.1.41 pullulanase, 3.2.1.42
GDP-glucosidase, 3.2.1.43 beta-L-rhamnosidase, 3.2.1.44
fucoidanase, 3.2.1.45 glucosylceramidase, 3.2.1.46
galactosylceramidase, 3.2.1.47
galactosylgalactosylglucosylceramidase, 3.2.1.48 sucrose
alpha-glucosidase, 3.2.1.49 alpha-N-acetylgalactosaminidase,
3.2.1.50 alpha-N-acetylglucosaminidase, 3.2.1.51
alpha-L-fucosidase, 3.2.1.52 beta-N-acetylhexosaminidase, 3.2.1.53
beta-N-acetylgalactosaminidase, 3.2.1.54 cyclomaltodextrinase,
3.2.1.55 alpha-N-arabinofuranosidase, 3.2.1.56
glucuronosyl-disulfoglucosamine glucuronidase, 3.2.1.57
isopullulanase, 3.2.1.58 glucan 1,3-beta-glucosidase, 3.2.1.59
glucan endo-1,3-alpha-glucosidase, 3.2.1.60 glucan
1,4-alpha-maltotetraohydrolase, 3.2.1.61 mycodextranase, 3.2.1.62
glycosylceramidase, 3.2.1.63 1,2-alpha-L-fucosidase, 3.2.1.64
2,6-beta-fructan 6-levanbiohydrolase, 3.2.1.65 levanase, 3.2.1.66
quercitrinase, 3.2.1.67 galacturan 1,4-alpha-galacturonidase,
3.2.1.68 isoamylase, 3.2.1.69 amylopectin 6-glucanohydrolase,
3.2.1.70 glucan 1,6-alpha-glucosidase, 3.2.1.71 glucan
endo-1,2-beta-glucosidase, 3.2.1.72 xylan 1,3-beta-xylosidase,
3.2.1.73 licheninase, 3.2.1.74 glucan 1,4-beta-glucosidase,
3.2.1.75 glucan endo-1,6-beta-glucosidase, 3.2.1.76 L-iduronidase,
3.2.1.77 mannan 1,2-(1,3)-alpha-mannosidase, 3.2.1.78 mannan
endo-1,4-beta-mannosidase, 3.2.1.79 alpha-L-arabinofuranoside
hydrolase, 3.2.1.80 fructan beta-fructosidase, 3.2.1.81
beta-agarase, 3.2.1.82 exo-poly-alpha-galacturonosidase, 3.2.1.83
kappa-carrageenase, 3.2.1.84 glucan 1,3-alpha-glucosidase, 3.2.1.85
6-phospho-beta-galactosidase, 3.2.1.86 6-phospho-beta-glucosidase,
3.2.1.87 capsular-polysaccharide endo-1,3-alpha-galactosidase,
3.2.1.88 beta-L-arabinosidase, 3.2.1.89 arabinogalactan
endo-1,4-beta-galactosidase, 3.2.1.90 arabinogalactan
endo-1,3-beta-galactosidase, 3.2.1.91 cellulose
1,4-beta-cellobiosidase, 3.2.1.92 peptidoglycan
beta-N-acetylmuramidase, 3.2.1.93 alpha,alpha-phosphotrehalase,
3.2.1.94 glucan 1,6-alpha-isomaltosidase, 3.2.1.95 dextran
1,6-alpha-isomaltotriosidase, 3.2.1.96 mannosylglycoprotein
endo-beta-N-acetylglucosaminidase, 3.2.1.97 glycopeptide
alpha-N-acetylgalactosaminidase, 3.2.1.98 glucan
1,4-alpha-maltohexaosidase, 3.2.1.99 arabinan
endo-1,5-alpha-L-arabinosidase, 3.2.1.100 mannan
1,4-mannobiosidase, 3.2.1.101 mannan endo-1,6-alpha-mannosidase,
3.2.1.102 blood-group-substance endo-1,4-beta-galactosidase,
3.2.1.103 keratan-sulfate endo-1,4-beta-galactosidase, 3.2.1.104
steryl-beta-glucosidase, 3.2.1.105 3alpha(S)-strictosidine
beta-glucosidase, 3.2.1.106 mannosyl-oligosaccharide glucosidase,
3.2.1.107 protein-glucosylgalactosylhydroxylysine glucosidase,
3.2.1.108 lactase, 3.2.1.109 endogalactosaminidase, 3.2.1.110
mucinaminylserine mucinaminidase, 3.2.1.111 1,3-alpha-L-fucosidase,
3.2.1.112 2-deoxyglucosidase, 3.2.1.113 mannosyl-oligosaccharide
1,2-alpha-mannosidase, 3.2.1.114 mannosyl-oligosaccharide
1,3-1,6-alpha-mannosidase, 3.2.1.115 branched-dextran
exo-1,2-alpha-glucosidase, 3.2.1.116 glucan
1,4-alpha-maltotriohydrolase, 3.2.1.117 amygdalin beta-glucosidase,
3.2.1.118 prunasin beta-glucosidase, 3.2.1.119 vicianin
beta-glucosidase, 3.2.1.120 oligoxyloglucan beta-glycosidase,
3.2.1.121 polymannuronate hydrolase, 3.2.1.122 maltose-6'-phosphate
glucosidase, 3.2.1.123 endoglycosylceramidase, 3.2.1.124
3-deoxy-2-octulosonidase, 3.2.1.125 raucaffricine beta-glucosidase,
3.2.1.126 coniferin beta-glucosidase, 3.2.1.127
1,6-alpha-L-fucosidase, 3.2.1.128 glycyrrhizinate
beta-glucuronidase, 3.2.1.129 endo-alpha-sialidase, 3.2.1.130
glycoprotein endo-alpha-1,2-mannosidase, 3.2.1.131 xylan
alpha-1,2-glucuronosidase, 3.2.1.132 chitosanase, 3.2.1.133 glucan
1,4-alpha-maltohydrolase, 3.2.1.134 difructose-anhydride synthase,
3.2.1.135 neopullulanase, 3.2.1.136 glucuronoarabinoxylan
endo-1,4-beta-xylanase, 3.2.1.137 mannan
exo-1,2-1,6-alpha-mannosidase, 3.2.1.138 anhydrosialidase,
3.2.1.139 alpha-glucuronidase, 3.2.1.140 lacto-N-biosidase,
3.2.1.141 4-alpha-D-{(1->4)-alpha-D-glucano}trehalose
trehalohydrolase, 3.2.1.142 limit dextrinase, 3.2.1.143
poly(ADP-ribose) glycohydrolase, 3.2.1.144 3-deoxyoctulosonase,
3.2.1.145 galactan 1,3-beta-galactosidase, 3.2.1.146
beta-galactofuranosidase, 3.2.1.147 thioglucosidase, 3.2.1.148
ribosylhomocysteinase, 3.2.1.149 beta-primeverosidase, 3.2.1.150
oligoxyloglucan reducing-end-specific cellobiohydrolase, 3.2.1.151
xyloglucan-specific endo-beta-1,4-glucanase, 3.2.1.152
mannosylglycoprotein endo-beta-mannosidase, 3.2.1.153 fructan
beta-(2,1)-fructosidase, 3.2.1.154 fructan beta-(2,6)-fructosidase,
3.2.1.155 xyloglucan-specific exo-beta-1,4-glucanase, 3.2.1.156
oligosaccharide reducing-end xylanase, 3.2.1.157 iota-carrageenase
3.2.1.158 alpha-agarase, 3.2.1.159 alpha-neoagaro-oligosaccharide
hydrolase, 3.2.1.160 xyloglucan-specific exo-beta-1,4-glucanase,
3.2.1.161 beta-apiosyl-beta-glucosidase, 3.2.1.162
lambda-carrageenase, 3.2.1.163 1,6-alpha-D-mannosidase, 3.2.1.164
galactan endo-1,6-beta-galactosidase, 3.2.1.165
exo-1,4-beta-D-glucosaminidase, or a combination thereof.
[0128] Other enzymes that are used in various embodiments of the
methods described herein include, by way of non-limiting example, a
sulfatase including, e.g., enzymes categorized as 3.1.6.X by BRENDA
(the comprehensive Enzyme Information System) including 3.1.6.1
arylsulfatase, 3.1.6.2 steryl-sulfatase, 3.1.6.3 glycosulfatase,
3.1.6.4 N-acetylgalactosamine-6-sulfatase, 3.1.6.5 sinigrin
sulfohydrolase; myrosulfatase, 3.1.6.6 choline-sulfatase, 3.1.6.7
cellulose-polysulfatase, 3.1.6.8 cerebroside-sulfatase, 3.1.6.9
chondro-4-sulfatase, 3.1.6.10 chondro-6-sulfatase, 3.1.6.11 di
sulfoglucosamine-6-sulfatase, 3.1.6.12
N-acetylgalactosamine-4-sulfatase, 3.1.6.13 iduronate-2-sulfatase,
3.1.6.14 N-acetylglucosamine-6-sulfatase, 3.1.6.15
N-sulfoglucosamine-3-sulfatase, 3.1.6.16 monomethyl-sulfatase,
3.1.6.17 D-lactate-2-sulfatase, 3.1.6.18 glucuronate-2-sulfatase,
3.10.1.1 N-sulfoglucosamine sulfohydrolase, or combinations
thereof.
[0129] Certain enzymes that are used in various embodiments of the
methods described herein include, by way of non-limiting example, a
deacetylase, e.g., an exo-deacetylase, including, by way of
non-limiting example, the alpha-glucosaminide N-acetyltransferase
(2.3.1.78) or similar enzymes.
[0130] Certain enzymes that are used in various embodiments of the
methods described herein include, by way of non-limiting example, a
carbohydrate phosphatase including, e.g., 3.1.3.1 alkaline
phosphatase, 3.1.3.2 acid phosphatase, 3.1.3.B2 diacylglycerol
pyrophosphate phosphatase, 3.1.3.3 phosphoserine phosphatase,
3.1.3.4 phosphatidate phosphatase, 3.1.3.5 5'-nucleotidase, 3.1.3.6
3'-nucleotidase, 3.1.3.7 3'(2'),5'-bisphosphate nucleotidase,
3.1.3.8 3-phytase, 3.1.3.9 glucose-6-phosphatase, 3.1.3.10
glucose-1-phosphatase, 3.1.3.11 fructose-bisphosphatase, 3.1.3.12
trehalose-phosphatase, 3.1.3.13 bisphosphoglycerate phosphatase,
3.1.3.14 methylphosphothioglycerate phosphatase, 3.1.3.15
histidinol-phosphatase, 3.1.3.16 phosphoprotein phosphatase,
3.1.3.17 [phosphorylase] phosphatase, 3.1.3.18 phosphoglycolate
phosphatase, 3.1.3.19 glycerol-2-phosphatase, 3.1.3.20
phosphoglycerate phosphatase, 3.1.3.21 glycerol-1-phosphatase,
3.1.3.22 mannitol-1-phosphatase, 3.1.3.23 sugar-phosphatase,
3.1.3.24 sucrose-phosphate phosphatase, 3.1.3.25 inositol-phosphate
phosphatase, 3.1.3.26 4-phytase, 3.1.3.27
phosphatidylglycerophosphatase, 3.1.3.28 ADP-phosphoglycerate
phosphatase, 3.1.3.29 N-acylneuraminate-9-phosphatase, 3.1.3.30
3'-phosphoadenylylsulfate 3'-phosphatase, 3.1.3.31 nucleotidase,
3.1.3.32 polynucleotide 3'-phosphatase, 3.1.3.33 polynucleotide
5'-phosphatase, 3.1.3.34 deoxynucleotide 3'-phosphatase, 3.1.3.35
thymidylate 5'-phosphatase, 3.1.3.36 phosphoinositide
5-phosphatase, 3.1.3.37 sedoheptulose-bisphosphatase, 3.1.3.38
3-phosphoglycerate phosphatase, 3.1.3.39
streptomycin-6-phosphatase, 3.1.3.40
guanidinodeoxy-scyllo-inositol-4-phosphatase, 3.1.3.41
4-nitrophenylphosphatase, 3.1.3.42 [glycogen-synthase-D]
phosphatase, 3.1.3.43 [pyruvate dehydrogenase
(acetyl-transferring)]-phosphatase, 3.1.3.44 [acetyl-CoA
carboxylase]-phosphatase, 3.1.3.45
3-deoxy-manno-octulosonate-8-phosphatase, 3.1.3.46
fructose-2,6-bisphosphate 2-phosphatase, 3.1.3.47
[hydroxymethylglutaryl-CoA reductase (NADPH)]-phosphatase, 3.1.3.48
protein-tyrosine-phosphatase, 3.1.3.49 [pyruvate
kinase]-phosphatase, 3.1.3.50 sorbitol-6-phosphatase, 3.1.3.51
dolichyl-phosphatase, 3.1.3.52 [3-methyl-2-oxobutanoate
dehydrogenase (2-methylpropanoyl-transferring)]-phosphatase,
3.1.3.53 [myosin-light-chain] phosphatase, 3.1.3.54
fructose-2,6-bisphosphate 6-phosphatase, 3.1.3.55
caldesmon-phosphatase, 3.1.3.56 inositol-polyphosphate
5-phosphatase, 3.1.3.57 inositol-1,4-bisphosphate 1-phosphatase,
3.1.3.58 sugar-terminal-phosphatase, 3.1.3.59
alkylacetylglycerophosphatase, 3.1.3.60 phosphoenolpyruvate
phosphatase, 3.1.3.61 inositol-1,4,5-trisphosphate 1-phosphatase,
3.1.3.62 multiple inositol-polyphosphate phosphatase, 3.1.3.63
2-carboxy-D-arabinitol-1-phosphatase, 3.1.3.64
phosphatidylinositol-3-phosphatase, 3.1.3.65
inositol-1,3-bisphosphate 3-phosphatase, 3.1.3.66
phosphatidylinositol-3,4-bisphosphate 4-phosphatase, 3.1.3.67
phosphatidylinositol-3,4,5-trisphosphate 3-phosphatase, 3.1.3.68
2-deoxyglucose-6-phosphatase, 3.1.3.69 glucosylglycerol
3-phosphatase, 3.1.3.70 mannosyl-3-phosphoglycerate phosphatase,
3.1.3.71 2-phosphosulfolactate phosphatase, 3.1.3.72 5-phytase,
3.1.3.73 alpha-ribazole phosphatase, 3.1.3.74 pyridoxal
phosphatase, 3.1.3.75 phosphoethanolamine/phosphocholine
phosphatase, 3.1.3.76 lipid-phosphate phosphatase, 3.1.3.77
acireductone synthase, 3.1.3.78
phosphatidylinositol-4,5-bisphosphate 4-phosphatase, or 3.1.3.79
mannosylfructose-phosphate phosphatase, or a combination
thereof.
[0131] In some embodiments, processes described herein include
incubation and digestion with a first enzyme to clear a specific
non-reducing end structure, incubation and digestion with a second
enzyme. In certain embodiments, this multi-enzyme approach is
useful in order to reduce the background. For example, in MPS II
treating the sample with an iduronidase and/or glucuronidase to
clear all non-sulfated non-reducing end uronic acids (this enzyme
will not cleave sulfated iduronic acids) before 2-O sulfatase
treatment. This approach will clear all non-sulfated non-reducing
end uronic acids so that upon desulfation with the 2-O sulfatase
the newly releasable uronic acids will be those that were
previously sulfated (and therefore resistant to the action of the
iduronidase and/or glucuronidase).
Glycan Residual Compounds:
[0132] Glycan residual compounds detected, measured, analyzed,
and/or otherwise characterized according to any process described
herein include any suitable glycan residue that is liberated from
the non-reducing end of a glycan (e.g., a glycan obtained from a
biological sample of an individual). In specific instances, glycan
residual compounds including, e.g., oligosaccharides,
monosaccharides, sulfate, phosphate, sialic acid, acetate, or the
like.
Specific glycan residual compounds useful in any process herein are
described in Tables 1-4.
[0133] In some embodiments, the generated biomarker is a glycan
residual compound. In some embodiments, the glycan residual
compound is a monosaccharide. In certain embodiments, the glycan
residual compound is sulfate, phosphate, acetate, or a combination
thereof. In certain embodiments, the glycan residual compound has a
molecular weight of less than 2000 g/mol, less than 1500 g/mol,
less than 1000 g/mol, less than 500 g/mol, less than 400 g/mol,
less than 300 g/mol, less than 260 g/mol, less than 200 g/mol, less
than 100 g/mol, or the like (e.g., prior to tagging with any
detectable label that may be included in a process described
herein).
Biomarker Ratios:
[0134] In various aspects provided herein, the simultaneous
measurement or ratios of various biomarkers (e.g., saturated
non-reducing end structures or internal unsaturated disaccharides
generated by enzymatic depolymerization of glycosaminoglycans)
reveals information about disease severity and response to therapy.
Depending on the specific disease being diagnosed or otherwise
analyzed, these comparisons (e.g., simultaneous measurement or
ratios) use varying saturated and unsaturated structures.
[0135] For example, in some embodiments, one or more of the
biomarkers used in any process described herein includes one of the
saturated biomarkers (glycan fragments) set forth in Table 1. In
specific embodiments, the disorder being diagnosed or otherwise
analyzed is MPS I. In some embodiments, the first and second
biomarkers are biomarkers of Table 1. In other embodiments, the
first biomarker is a biomarker of Table 1 and the second biomarker
is a biomarker of Table 9, 3, 4, or 6. In further or alternative
embodiments, both the first and second biomarkers are from Table
1.
TABLE-US-00001 TABLE 1 HS derived CS/DS derived IdoA-GlcNS
IdoA-GalNAc4S IdoA-GlcNS6S IdoA-GalNAc6S IdoA-GlcNAc IdoA-GalNAc
IdoA-GlcNAc6S IdoA-GalNAc4S6S
[0136] In further embodiments, one or more of the biomarkers used
in any process described herein includes one of the saturated
biomarkers (glycan fragments) set forth in Table 2. In specific
embodiments, the disorder being diagnosed or otherwise analyzed is
MPS II. In some embodiments, the first biomarker is a biomarker of
Table 2 and the second biomarker is a biomarker of Table 1. In
other embodiments, the first biomarker is a biomarker of Table 2
and the second biomarker is a biomarker of Table 9. In further or
alternative embodiments, both the first and second biomarkers are
from Table 2.
TABLE-US-00002 TABLE 2 HS derived CS/DS derived IdoA2S-GlcNS
IdoA2S-GalNAc4S IdoA2S-GlcNS6S IdoA2S-GalNAc6S IdoA2S-GlcNAc
IdoA2S-GalNAc IdoA2S-GlcNAc6S IdoA2S-GalNAc4S6S
[0137] In further embodiments, one or more of the biomarkers used
in any process described herein includes one of the saturated
biomarkers (glycan fragments) set forth in Table 3. In specific
embodiments, the disorder being diagnosed or otherwise analyzed is
MPS IIIA. In some embodiments, the first biomarker is a biomarker
of Table 3 and the second biomarker is a biomarker of Table 5. In
other embodiments, the first biomarker is a biomarker of Table 3
and the second biomarker is a biomarker of Table 9. In further or
alternative embodiments, both the first and second biomarkers are
from Table 3.
TABLE-US-00003 TABLE 3 HS derived GlcNS
GlcNS+/-6S-UA+/-2S-GlcNAc+/-6S GlceNS+/-6S-UA+/-2S-GlcNS+/-6S
[0138] In further embodiments, one or more of the biomarkers used
in any process described herein includes one of the saturated
biomarkers (glycan fragments) set forth in Table 4. In specific
embodiments, the disorder being diagnosed or otherwise analyzed is
MPS IIIB. In some embodiments, the first biomarker is a biomarker
of Table 4 and the second biomarker is a biomarker of Table 1, 2,
or 8. In other embodiments, the first biomarker is a biomarker of
Table 4 and the second biomarker is a biomarker of Table 9. In
further or alternative embodiments, both the first and second
biomarkers are from Table 4.
TABLE-US-00004 TABLE 4 HS derived GlcNAc GlcNAc-UA+/-2S-GlcNAc+/-6S
GlcNAc-UA+/-2S-GlcNS+/-6S
[0139] In further embodiments, one or more of the biomarkers used
in any process described herein includes one of the saturated
biomarkers (glycan fragments) set forth in Table 5. In specific
embodiments, the disorder being diagnosed or otherwise analyzed is
MPS IIIC. In some embodiments, the first biomarker is a biomarker
of Table 5 and the second biomarker is a biomarker of Table 4. In
other embodiments, the first biomarker is a biomarker of Table 5
and the second biomarker is a biomarker of Table 9. In further or
alternative embodiments, both the first and second biomarkers are
from Table 5.
TABLE-US-00005 TABLE 5 HS derived GlcN
GlcN+/-6S-UA+/-2S-GlcNAc+/-6S GlcN+/-6S-UA+/-2S-GlcNS+/-6S
[0140] In further embodiments, one or more of the biomarkers used
in any process described herein includes one of the saturated
biomarkers (glycan fragments) set forth in Table 6. In specific
embodiments, the disorder being diagnosed or otherwise analyzed is
MPS IIID. In some embodiments, the first biomarker is a biomarker
of Table 6 and the second biomarker is a biomarker of Table 4 or 5.
In other embodiments, the first biomarker is a biomarker of Table 6
and the second biomarker is a biomarker of Table 9. In further or
alternative embodiments, both the first and second biomarkers are
from Table 6.
TABLE-US-00006 TABLE 6 HS derived GlcN6S GlcNAc6S
GlcN6S-UA+/-2S-GlcNAc+/-6S GlcNAc6S-UA+/-2S-GlcNAc+/-6S
GlcN6S-UA+/-2S-GlcNS+/-6S GlcNAc6S-UA+/-2S-GlcNS+/-6S
[0141] In further embodiments, one or more of the biomarkers used
in any process described herein includes one of the saturated
biomarkers (glycan fragments) set forth in Table 7. In specific
embodiments, the disorder being diagnosed or otherwise analyzed is
MPS VI. In some embodiments, the first biomarker is a biomarker of
Table 7 and the second biomarker is a biomarker of Table 8. In
other embodiments, the first biomarker is a biomarker of Table 7
and the second biomarker is a biomarker of Table 9. In further or
alternative embodiments, both the first and second biomarkers are
from Table 7.
TABLE-US-00007 TABLE 7 CS derived GalNAc4S GalNAc4S-UA-GalNAc
GalNAc4S-UA-GalNAc4S GalNAc4S-UA-GalNAc6S GalNAc4S-UA-GalNAc4S6S
GalNAc4S-UA2S-GalNAc GalNAc4S-UA2S-GalNAc4S GalNAc4S-UA2S-GalNAc6S
GalNAc4S-UA2S-GalNAc4S6S
[0142] In further embodiments, one or more of the biomarkers used
in any process described herein includes one of the saturated
biomarkers (glycan fragments) set forth in Table 8. In specific
embodiments, the disorder being diagnosed or otherwise analyzed is
MPS VII. In some embodiments, the first biomarker is a biomarker of
Table 8 and the second biomarker is a biomarker of Table 3, 4, 6,
or 7. In other embodiments, the first biomarker is a biomarker of
Table 8 and the second biomarker is a biomarker of Table 9. In
further or alternative embodiments, both the first and second
biomarkers are from Table 1.
TABLE-US-00008 TABLE 8 HS derived CS derived KS derived GlcA-GlcNAc
GlcA-GalNAc Gal-GlcNAc GlcA-GlcNS GlcA-GalNAc4S Gal-GlcNAc6S
GlcA-GlcNAc6S GlcA-GalNAc6S Gal6S-GlcNAc GlcA-GlcNS6S
GlcA-GalNAc4S6S Gal6S-GlcNAc6S GlcNAc-Gal GlcNAc-Gal6S GlcNAc6S-Gal
GlcNAc6S-Gal6S
[0143] In further embodiments, one or more of the biomarkers used
in any process described herein includes one of the unsaturated
biomarkers (glycan fragments) set forth in Table 9. In further or
alternative embodiments, both the first and second biomarkers are
from Table 9.
TABLE-US-00009 TABLE 9 HS derived CS derived .DELTA.UA-GlcN
.DELTA.UA-GalNAc .DELTA.UA-GlcN6S .DELTA.UA-GalNAc4S
.DELTA.UA2S-GlcN .DELTA.UA-GalNAc6S .DELTA.UAS-GlcN6S
.DELTA.UA2S-GalNAc .DELTA.UA-GlcNAc .DELTA.UA2S-GalNAc4S
.DELTA.UA-GlcNAc6S .DELTA.UA2S-GalNAc6S .DELTA.UA2S-GlcNAc
.DELTA.UA-GalNAc4S6S .DELTA.UA2S-GlcNAc6S .DELTA.UA2S-GalNAc4S6S
.DELTA.UA-GlcNS .DELTA.UA-GlcNS6S .DELTA.UA-GlcNS3S
.DELTA.UA2S-GlcNS .DELTA.UA2S-GlcNS6S .DELTA.UA2S-GlcNS3S
.DELTA.UA-GlcNS6S3S .DELTA.UA2S-GlcNS6S3S
[0144] In further embodiments, one or more of the biomarkers used
in any process described herein includes one of the saturated
biomarkers (glycan fragments) set forth in Table 10. In specific
embodiments, the disorder being diagnosed or otherwise analyzed is
MPS IVA. In some embodiments, the first biomarker is a biomarker of
Table 10 and the second biomarker is a biomarker of Table 8. In
other embodiments, the first biomarker is a biomarker of Table 10
and the second biomarker is a biomarker of Table 9. In further or
alternative embodiments, both the first and second biomarkers are
from Table 10.
TABLE-US-00010 TABLE 10 KS derived CS Derived Gal6S GalNAc6S
Gal6S-GlcNAc GalNAc6S4S Gal6S-GlcNAc6S GalNAc6S-UA-GalNAc
Gal6S-GlcNAc-Gal GalNAc6S-UA-GalNAc4S Gal6S-GlcNAc-Gal6S
GalNAc6S-UA-GalNAc6S Gal6S-GlcNAc6S-Gal GalNAc6S-UA-GalNAc4S6S
Gal6S-GlcNAc6S-Gal6S GalNAc6S-UA25-GalNAc GalNAc6S-UA2S-GalNAc4S
GalNAc6S-UA2S-GalNAc6S GalNAc6S-UA2S-GalNAc4S6S
GalNAc6S4S-UA-GalNAc GalNAc6S4S-UA-GalNAc4S GalNAc6S4S-UA-GalNAc6S
GalNAc6S4S-UA-GalNAc4S6S GalNAc6S4S-UA25-GalNAc
GalNAc6S4S-UA2S-GalNAc4S GalNAc6S4S-UA2S-GalNAc6S
GalNAc6S4S-UA2S-GalNAc4S6S
[0145] In further embodiments, one or more of the biomarkers used
in any process described herein includes one of the saturated
biomarkers (glycan fragments) set forth in Table 11. In specific
embodiments, the disorder being diagnosed or otherwise analyzed is
MPS IVB. In some embodiments, the first biomarker is a biomarker of
Table 11 and the second biomarker is a biomarker of Table 8. In
other embodiments, the first biomarker is a biomarker of Table 11
and the second biomarker is a biomarker of Table 9. In further or
alternative embodiments, both the first and second biomarkers are
from Table 11.
TABLE-US-00011 TABLE 11 KS derived CS Derived Glyco-lipid derived
Gal GalNAc Gal-GalNAc-Gal-Glu Gal-GlcNAc GalNAc4S Gal-GalNAc-Gal-
Glu + 1 Sialic acid Gal-GlcNAc6S GalNAc-UA-GalNAc Gal-GalNAc-Gal-
Glu + 2 Sialic acids Gal-GlcNAc-Gal GalNAc-UA-GalNAc4S
Gal-GalNAc-Gal- Glu + 3 Sialic acids Gal-GlcNAc-Gal6S
GalNAc-UA-GalNAc6S Gal-GlcNAc6S-Gal GalNAc-UA-GalNAc4S6S
Gal-GlcNAc6S- GalNAc-UA25-GalNAc Gal6S GalNAc-UA2S-GalNAc4S
GalNAc-UA2S-GalNAc6S GalNAc-UA25- GalNAc4S6S GalNAc4S-UA-GalNAc
GalNAc4S-UA-GalNAc4S GalNAc4S-UA-GalNAc6S GalNAc4S-UA- GalNAc4S6S
GalNAc4S-UA25-GalNAc GalNAc4S-UA2S- GalNAc4S GalNAc4S-UA2S-
GalNAc6S GalNAc4S-UA2S- GalNAc4S6S
[0146] As used herein, IdoA and are iduronic acid (e.g.,
.alpha.-L-iduronic acid) saccharide residues. As used herein, GlcA
and are glucuronic acid (e.g., .beta.-L-glucuronic acid) saccharide
residues. As used herein, are unsaturated uronic acids (UA), such
as IdoA and GlcA. As used herein, GlcN and are glucosamine (e.g.,
2-deoxy-2-amino-.beta.-D-glucopyranosyl) saccharide residues. As
used herein, GlcN(Ac)1 and are a glucosamine (e.g.,
2-deoxy-2-amino-.beta.-D-glucopyranosyl) saccharide residue wherein
the 2-amino group is acetylated. As used herein, Gal and
.largecircle. is a galactose saccharide residue. In various
specific instances, iduronic acid, glucuronic acid, glucosamine,
and/or galactose saccharide residues are saturated at 4 and 5
carbons of the non-reducing end saccharide residue, or are free of
carbon-carbon unsaturation. In other instances, any one or more of
the saccharide residues is unsaturated, e.g., at the 4 and 5 carbon
positions of the saccharide residue at the non-reducing end of an
oligosaccharide provided herein. The symbolic nomenclature used
herein follows the "Symbol and Text Nomenclature for Representation
of Glycan Structure" as promulgated by the Nomenclature Committee
for the Consortium for Functional Glycomics, as amended on October
2007.
[0147] As an illustrative example of non-reducing end saccharide
residues that are saturated and unsaturated at the C4 and C5
positions, an L-iduronic acid (IdoA) residue that is saturated at
the C4 and C5 positions has a structure as follows:
##STR00001##
whereas an L-iduronic acid (IdoA) residue at the non-reducing end
of the oligosaccharide that is unsaturated at the C4 and C5
positions may have a structure as follows:
##STR00002##
or the like. Oligosaccharides having non-reducing end saccharide
residues that are saturated at the C4 and C5 position are referred
to herein as "C4-C5 non-reducing end saturated
oligosaccharides".
Ratios of NRE Biomarkers:
[0148] In certain embodiments, a method provided for herein
comprises comparing a first biomarker that is an NRE biomarker to a
second biomarker that is a different NRE biomarker. In some
embodiments, the first biomarker is specific to a particular
disease (e.g., MPS disease or other disease associated with altered
GAG synthesis or degradation). In certain embodiments, the second
biomarker is an NRE biomarker that would not be expected for the
particular disease (e.g., according to the tables provided
herein).
[0149] In some embodiments, a method described herein is used in
concert with an ERT therapy. In some of such embodiments, the
method is utilized to monitor the efficacy of an ERT therapy.
[0150] In certain aspects, by examining the ratio of abundance of a
disease specific NRE(s) to the NRE(s) that are generated after the
action of an enzyme replacement therapy (ERT) in use, one can
verify that the ERT is acting in the desired cellular compartment
(the lysosome). In some instances, this is important in order to
ensure that a reduction in the glycan substrate in response to
treatment reflects the beneficial action of the ERT in the lysosome
or the non-therapeutically beneficial action of the enzyme outside
of the lysosome. This is especially important in therapeutic
approaches that require sampling fluids for biomarker analysis
through the same port that the ERT was delivered--such as
intrathecal delivery of ERT. If the ERT is acting outside of the
cell (in blood, CSF, or in a sampling port) the subsequent
lysosomal enzymes will not efficiently degrade the resulting
glycan. This leads to the elimination of the disease specific NRE
and generation of a NRE typically associated with a different
disease.
[0151] For example, in one specific embodiment, the disease being
diagnosed or otherwise analyzed is MPS II. In some of such
instances, the first biomarker is an MPS II disease specific NRE
biomarker, such as IdoA2S-GlcN(+/-NS, +/-6S). If the ERT
(2-sulfatase) acts in the lysosome, this NRE is 2-O desulfated
producing IdoA-GlcN(+/-NS, +/-6S) which is rapidly eliminated by
the subsequent lysosomal enzymes that are functional in MPS II
patients. In contrast, if the ERT acts outside of the lysosome, the
first biomarker (the MPS II NRE biomarker) [IdoA2S-GlcN(+/-NS,
+/-6S)] is eliminated and the second biomarker (e.g., an MPS I NRE,
such as [IdoA-GlcN(+/-NS, +/-6S)]) is generated (the extracellular
action NRE, EANRE). In some instances, because the other lysosomal
enzymes are not present in significant active quantities outside of
the lysosome, the MPS I markers are stable. In some cases the NREs
can be converted to other NRE structures through the action of
other endogenous enzymes. In some aspects, using such techniques
and by simultaneous monitoring of the MPS II and MPS I NREs, the
severity of disease and specific response to therapy are
determined. Similar methods for the other MPS disorders, or any
other disorder involving abnormal glycan accumulation,
biosynthesis, and/or degradation are contemplated herein.
[0152] In exemplary embodiments, the generation of an MPS I NRE
biomarker in an MPS II patient after ERT treatment indicates that
the ERT is not effectively acting in the lysosome. In various
aspects, the disease specific NRE and EANRE ratios that are
relevant to each disease are different for each disease class
dependent on the NRE of the target disease and the relevant EANREs
that are generated by the ERT. In specific exemplary embodiments
methods described herein utilize the following specific first and
second biomarkers when utilized with the denoted disease: [0153]
MPS I [0154] Disease specific NREs (saturated fragments) [0155]
Disaccharides IdoA-GlcN(+/-NS, +/-6S) [0156] EANREs [0157] Mono and
trisaccharides from the MPS IIIA and MPS IIIB family [0158] MPS II
[0159] Disease specific NREs (saturated fragments) [0160]
Disaccharides IdoA2S-GlcN(+/-NS, +/-6S) [0161] EANREs [0162]
Disaccharides from the MPS I family [0163] MPS IIIA [0164] Disease
specific NREs (saturated fragments) [0165] Trisaccharides:
GlcNS-GlcA/IdoA(+/-2S)-GlcN(+/-NS, +/-6S) [0166] EANREs [0167]
Disaccharides from the MPS IIIC family [0168] MPS IIIB [0169]
Disease specific NREs (saturated fragments) [0170] Trisaccharides:
GlcNAc-GlcA/IdoA(+/-2S)-GlcN(+/-NS, +/-6 S) [0171] EANREs [0172]
Disaccharides from the MPS I, II and VII families [0173] MPS IIIC
[0174] Disease specific NREs (saturated fragments) [0175]
Trisaccharides: GlcN-GlcA/IdoA(+/-2S)-GlcN(+/-NS, +/-6S) [0176]
EANREs [0177] Disaccharides from the MPS IIIB family [0178] MPS
IIID [0179] Disease specific NREs (saturated fragments) [0180]
Trisaccharides: GlcN(+/-NS)6S-GlcA/IdoA(+/-2S)-GlcN(+/-NS, +/-6S)
[0181] EANREs [0182] Disaccharides from the MPS IIIA and IIIB
families [0183] MPS IVA [0184] Disease specific NREs (saturated
fragments) [0185] KS derived mono-, di, and trisaccharides: Gal6S,
Gal6S-GlcNAc(+/-6S), Gal6S-UA(+/-2S)-Gal(+/-6S) [0186] CS derived
mono-, di, and trisaccharides: GalNAc6S(+/-4S),
GalNAc6S(+/-4S)-UA(+/-2S)-GalNAc(+/-4S, +/-6S) [0187] EANREs [0188]
Mono and disaccharides from the MPS IVB family [0189] MPS VI [0190]
Disease specific NREs (saturated fragments) [0191] CS derived mono
and trisaccharides: GalNAc4S, GalNAc4S-UA(+/-2S)-GalNAc(+/-4S,
+/-6S) [0192] EANREs [0193] NREs from hexosaminidase deficiencies
[0194] MPS VII [0195] Disease specific NREs (saturated fragments)
[0196] Disaccharides: GlcA-GlcN(+/-NS, +/-6S) [0197] EANREs [0198]
Disaccharides from the MPS IIIA, IIIB, and IIID families
Ratios of NRE and Non-NRE Biomarkers:
[0199] In certain embodiments, a method provided for herein
comprises comparing a first biomarker that is an NRE biomarker to a
second biomarker that is a non-NRE biomarker (e.g., a reducing end
or internal glycan residual biomarker). In some embodiments, the
first biomarker is specific to a particular disease (e.g., MPS
disease). In specific embodiments, the second biomarker is an
internal biomarker (e.g., from Table 9). In more specific
embodiments, such methods are utilized in combination with a
therapy for the treatment of a disorder associated with abnormal
glycan biosynthesis, degradation, and/or accumulation.
[0200] In certain embodiments, the second biomarker is a non-NRE
marker (e.g., rather than an EANRE discussed above). Because the
non-therapeutic action of the ERT only eliminates the specific NRE
structure, but does not reduce the level of the accumulating
glycan, ratios of the disease specific NRE to other non-NRE
structures can also be used to determine the site of action of the
ERT.
[0201] In an exemplary embodiment, wherein the disease being
diagnosed or otherwise analyzed is MPS II, a disease specific NRE
is IdoA2S-GlcN(+/-NS, +/-6S). If the ERT (2-sulfatase) acts in the
lysosome, this NRE is 2-O desulfated producing a GAG fragment that
terminates with IdoA-GlcN(+/-NS, +/-6S). That fragment is rapidly
eliminated by the subsequent lysosomal enzymes that are functional
in MPS II patients. In contrast, if the ERT acts outside of the
lysosome, the abundance of internal HS fragments liberated by lyase
digestion remain constant. Therefore, by simultaneous monitoring of
the MPS II and internal HS derived structures such as
.DELTA.UA-GlcNAc or .DELTA.UA-GlcNS the true lysosomal activity of
the treatment can be measured.
[0202] In some embodiments, a method described herein is utilized
to determine the severity of a disease described herein. In some of
such embodiments, the ratios of abundance of different biomarkers
(e.g., NRE biomarkers) may be analyzed and utilized to determine
disease severity and/or response to therapy.
[0203] For example, each MPS class has a number of specific NRE
structures that accumulate. In some embodiments, the ratio of the
different specific structures change as the disease severity
changes. For example in MPS II there are a number of HS derived
NREs (IdoA2S-GlcNS, IdoA2S-GlcNS6S, IdoA2S-GlcNAc, IdoA2S-GlcNAc6S)
and CS/DS derived NREs (IdoA2S-GalNAc4S, IdoA2S-GalNAc6S,
IdoA2S-GalNAc, IdoA2S-GalNAc4S6S) which are found in different
abundance depending on the severity of disease. By monitoring the
ratio of these distinct NRE structures, information about the
severity of the disease and response to therapy can be
obtained.
[0204] In some embodiments, a method described herein is utilized
to identify disease. In specific embodiments, ratios of NRE
biomarkers or Internal GAG lyase generated biomarkers are utilized
in such methods. In specific instances, the ratios of abundance of
different NRE and internal unsaturated saccharides generated after
lyase digestion can be used to indicate the presence of human
disease.
[0205] In specific embodiments, a method described herein is
utilized to identify Schneckenbecken dysplasia (which leads to
reduced UDP sugar donors which alters ratios of glycosaminoglycan
lyase generated fragments originating from HS, CS, and DS). In
other exemplary embodiments, a deficiency in an enzyme required for
the 2-O sulfation of heparan sulfate can be identified by examining
the ratio of unsaturated 2-O sulfated disaccharides (generated by
lyase digestion) to non-2-O sulfated disaccharides. In some
instances, a reduction in this ratio indicates the disruption of
heparan sulfate 2-O sulfation and the presence of human disease. In
further exemplary embodiments, a deficiency in the biosynthesis of
4-O sulfated chondroitin and dermatan sulfate can be identified by
examining the ratio of unsaturated 4-O sulfated disaccharides
(generated after lyase digestion to non-4-O sulfated
disaccharides). In some instances, a reduction in this ratio
indicates the disruption of chondroitin sulfate 4-O sulfation and
the presence of human disease. In still further exemplary
embodiments, a deficiency in PAPs (3-prime-phosphoadenosine
5-prime-phosphosulfate) synthesis or transport can be identified in
changes in the ratio of abundance or ratios of lyase generated
glycosaminoglycan fragments.
Disorders:
[0206] In certain embodiments, a disorder associated with abnormal
glycan accumulation includes a disorder associated therewith is
caused by an abnormally functioning glycan degradation enzyme. In
various embodiments, the abnormally functioning glycan degradation
enzyme functions abnormally as a result of being present in an
abnormally low amount, functioning improperly, or a combination
thereof. For example, an abnormally functioning glycan degradation
enzyme functions abnormally as a result of being present in an
amount of less than 50%, less than 40%, less than 30%, less than
20%, less than 10%, or less than 5% than is present in an
individual with normal amounts of the glycan degradation enzyme
(e.g., an individual in a non-diseased, normal, or wild type
state). In further or alternative embodiments, abnormally
functioning glycan degradation enzymes are present in a normal
amount, but do not function properly in degrading glycans. For
example, such enzymes may be have amino acid substitutions in the
sequences thereof that reduce or eliminate the glycan degradative
properties of the enzyme.
[0207] MPS I is a human genetic disease caused by a deficiency in
the lysosomal enzyme L-iduronidase. This enzyme is required in the
lysosome to degrade glycans that contain iduronic acid. Due to this
enzymatic deficiency, glycans with an iduronic acid on the
non-reducing end accumulate to high levels (including heparan
sulfate and dermatan sulfate). In certain embodiments, using the
method described herein, MPS I is diagnosed in an individual from a
biological sample taken therefrom. For example, in some
embodiments, a biological sample is optionally placed into a
defined MW cut off spin column (retains large molecules when spun),
optionally washed (e.g., with water or buffer) to remove free
monosaccharides, then treated with an iduronidase (e.g., to
liberate a glycan residual compound iduronic acid). In certain
embodiments, after incubation, the liberated iduronic acid is
isolated, e.g., by washing the free monosaccharide through the
defined MW cut off membrane (or other methods). In some of such
embodiments, the monosaccharide would be in the flow through. The
isolated monosaccharide solution is optionally dried or otherwise
treated to concentrate the sample and subsequently analyzed for
iduronic acid content by any suitable analytical technique (e.g.,
HPLC, MS, GC, or the like with or without chemical or enzymatic
derivatization before detection). This method can be used to detect
MPS I disease, measure disease severity, or to measure response to
therapy.
[0208] MPS II is a human genetic disease caused by a deficiency in
the lysosomal enzyme 2-sulfatase. This enzyme is required in the
lysosome to degrade glycans that contain 2-O sulfated uronic acids.
Due to this enzymatic deficiency, glycans with a 2-sulfated uronic
acid on the non-reducing end accumulate to high levels (including
heparan sulfate and dermatan sulfate). In certain embodiments,
using the method described herein, MPS II is diagnosed in an
individual from a biological sample taken therefrom. For example,
in some embodiments, a biological sample is optionally placed in to
a defined MW cut off spin column (retains large molecules when
spun), optionally washed (e.g., with 1 or more volumes of water or
buffer to remove free sulfate), and treated with a 2-sulfatase
(e.g., to liberate a glycan residual compound sulfate). In some
embodiments, after incubation, the liberated sulfate is optionally
isolated by washing the free monosaccharide (e.g., through a
defined MW cut off membrane or by any other suitable method). In
some of such embodiments, the free sulfate is in the flow through.
In certain embodiments, the resulting isolated solution is
optionally dried or otherwise treated to concentrate the sample and
subsequently analyzed for sulfate content by any suitable
analytical technique (e.g., HPLC, MS, GC, pH detection, or the like
with or without chemical or enzymatic derivatization before
detection). This method can be used to detect MPS II disease,
measure disease severity, or to measure response to therapy. In
other exemplary embodiments, following treatment with a
2-sulfatase, the resulting 2-O desulfated non-reducing end uronic
acid residues is optionally liberated with an iduronidase or
glucuronidase. In some of such embodiments, the resulting liberated
monosaccharide is optionally isolated, e.g., by washing free
monosaccharide (e.g., through the defined MW cut off membrane or
any other suitable method). In some of such embodiments, free
iduronic or glucuronic acid is in the flow through. In certain
embodiments, the resulting isolated solution is optionally dried or
otherwise treated to concentrate the sample and subsequently
analyzed for monosaccharide content by any suitable analytical
technique (e.g., HPLC, MS, GC, or the like with or without chemical
or enzymatic derivatization before detection). This method can be
used to detect MPS II disease, measure disease severity, or to
measure response to therapy.
[0209] MPS IIIA is a human genetic disease caused by a deficiency
in the lysosomal enzyme N-sulfatase. This enzyme is required in the
lysosome to degrade glycans that contain N-sulfated glucosamine
residues. Due to this enzymatic deficiency, glycans with N-sulfated
glucosamine residues on the non-reducing end accumulate to high
levels (including heparan sulfate). In certain embodiments, using
the method described herein, MPS IIIA is diagnosed in an individual
from a biological sample taken therefrom. For example, in some
embodiments, a biological sample is optionally placed in to a
defined MW cut off spin column (retains large molecules when spun),
optionally washed (e.g., with 1 or more volumes of water or buffer)
to remove free sulfate, and treated with an N-sulfatase. In certain
embodiments, after incubation, the liberated sulfate is optionally
isolated, e.g., by washing the free monosaccharide (such as through
a defined MW cut off membrane or any other suitable method). In
some of such embodiments, free sulfate for detection and/or
quantitation in the flow through. In certain embodiments, the
resulting isolated solution is optionally dried or otherwise
treated to concentrate the sample and subsequently analyzed for
sulfate content by any suitable analytical technique (e.g., HPLC,
MS, GC, pH detection, or the like with or without chemical or
enzymatic derivatization before detection). This method can be used
to detect MPS IIIA disease, measure disease severity, or to measure
response to therapy. In further or alternative embodiments,
following treatment with an N-sulfatase, the resulting N-desulfated
non-reducing end glucosamine residues is optionally liberated with
a hexosaminidase. In some of such embodiments, liberated
monosaccharide is optionally isolated (e.g., by washing the free
monosaccharide, such as through the defined MW cut off membrane or
any other suitable method). In some of such embodiments, free
glucosamine for detection and/or quantitation is present in the
flow through. In certain embodiments, the resulting isolated
solution is optionally dried or otherwise treated to concentrate
the sample and subsequently analyzed for monosaccharide content by
any suitable analytical technique (e.g., HPLC, MS, GC, or the like
with or without chemical or enzymatic derivatization before
detection). This method can be used to detect MPS IIIA disease,
measure disease severity, or to measure response to therapy.
[0210] As discussed above, in certain embodiments, using the method
described herein, MPS IIIA is diagnosed in an individual from a
biological sample taken therefrom. For example, in some
embodiments, a biological sample is optionally placed in to a
defined MW cut off spin column (retains large molecules when spun),
optionally washed (e.g., with 1 or more volumes of water or buffer)
to remove free monosaccharide, and treated with an N-sulfo
glucosaminidase such as a heparin lyase. In some embodiments,
liberated sulfated monosaccharide is optionally isolated, e.g., by
washing the free monosaccharide (such as through the defined MW cut
off membrane or by any other suitable method). In some of such
embodiments, free N-sulfated glucosamine for detection and/or
quantitation is present in the flow through. In certain
embodiments, the resulting isolated solution is optionally dried or
otherwise treated to concentrate the sample and subsequently
analyzed for monosaccharide content by any suitable analytical
technique (e.g., HPLC, MS, GC, or the like with or without chemical
or enzymatic derivatization before detection). This method can be
used to detect MPS IIIA disease, measure disease severity, or to
measure response to therapy.
[0211] As discussed above, in certain embodiments, using the method
described herein, MPS IIIA is diagnosed in an individual from a
biological sample taken therefrom. For example, in some
embodiments, a biological sample is optionally placed in to a
defined MW cut off spin column (retains large molecules when spun),
optionally washed (e.g., with 1 or more volumes of water or buffer)
to remove free monosaccharide, and treated with an N-sulfatase. In
certain embodiments, the resulting glycan is subsequently treated
such that the N-desulfated non-reducing end glucosamine residues is
acetylated (e.g., with an N-acetyl transferase) and subsequently
liberated with a hexosaminidase. In some of such embodiments, the
resulting liberated monosaccharide is optionally isolated, e.g., by
washing the free monosaccharide (e.g., through a defined MW cut off
membrane or any other suitable methods). In some of such
embodiments, free N-acetyl glucosamine for detection and/or
quantitation is present in the flow through. In certain
embodiments, the resulting isolated composition is optionally dried
or otherwise treated to concentrate the sample and subsequently
analyzed for monosaccharide content by any suitable analytical
technique (e.g., HPLC, MS, GC, or the like with or without chemical
or enzymatic derivatization before detection). This method can be
used to detect MPS IIIA disease, measure disease severity, or to
measure response to therapy.
[0212] MPS IIIB is a human genetic disease caused by a deficiency
in the enzyme N-acetyl glucosaminidase. This enzyme is required in
the lysosome to degrade glycans that contain N-acetyl glucosamine
residues. Due to this enzymatic deficiency, glycans with a N-acetyl
glucosamine residue on the non-reducing end accumulate to high
levels (including heparan sulfate). In certain embodiments, using
the method described herein, MPS IIIB is diagnosed in an individual
from a biological sample taken therefrom. For example, in some
embodiments, a biological sample is optionally placed in to a
defined MW cut off spin column (retains large molecules when spun),
optionally washed (e.g., with 1 or more volumes of water or buffer
to remove free N-acetyl glucosamine), and treated with a-acetyl
glucosaminidase or a heparin lyase (e.g., to liberate a glycan
residual compound N-acetyl glucosamine). In some embodiments, after
incubation, the liberated N-acetyl glucosamine is optionally
isolated by washing the free monosaccharide (e.g., through a
defined MW cut off membrane or by any other suitable method). In
some of such embodiments, the free monosaccharide is in the flow
through. In certain embodiments, the resulting isolated solution is
optionally dried or otherwise treated to concentrate the sample and
subsequently analyzed for monosaccharide content by any suitable
analytical technique (e.g., HPLC, MS, GC, pH detection, or the like
with or without chemical or enzymatic derivatization before
detection). This method can be used to detect MPS IIIB disease,
measure disease severity, or to measure response to therapy.
[0213] As discussed above, in certain embodiments, using the method
described herein, MPS IIIA is diagnosed in an individual from a
biological sample taken therefrom. For example, in some
embodiments, a biological sample is optionally placed in to a
defined MW cut off spin column (retains large molecules when spun),
optionally washed (e.g., with 1 or more volumes of water or buffer)
to remove free acetate, and treated with a deacetylase. The
liberated acetate is optionally isolated, e.g., by washing the free
acetate (such as through the defined MW cut off membrane or any
other suitable method). In some of such embodiments, the free
acetate for detection and/or quantitation is present the flow
through. In some embodiments, the resulting isolated solution is
optionally dried or otherwise treated to concentrate the sample and
subsequently analyzed for acetate content by any suitable
analytical technique (e.g., HPLC, MS, GC, pH detection, or the like
with or without chemical or enzymatic derivatization before
detection). This method can be used to detect MPS IIIB disease,
measure disease severity, or to measure response to therapy.
[0214] MPS IIIC is a human genetic disease caused by a deficiency
in the enzyme N-acetyltransferase. This enzyme is required in the
lysosome to degrade glycans that contain glucosamine residues. Due
to this enzymatic deficiency, glycans with a glucosamine residue on
the non-reducing end accumulate to high levels (including heparan
sulfate). In certain embodiments, using the method described
herein, MPS IIIC is diagnosed in an individual from a biological
sample taken therefrom. For example, in some embodiments, a
biological sample is optionally placed in to a defined MW cut off
spin column (retains large molecules when spun), optionally washed
(e.g., with 1 or more volumes of water or buffer to remove free
glucosamine), and treated with a hexosaminidase or heparin lyase
(e.g., to liberate a glycan residual compound glucosamine). In some
embodiments, after incubation, the liberated glucosamine is
optionally isolated by washing the free glucosamine (e.g., through
a defined MW cut off membrane or by any other suitable method). In
some of such embodiments, the free glucosamine for detection and/or
quantitation is present in the flow through. In certain
embodiments, the resulting isolated solution is optionally dried or
otherwise treated to concentrate the sample and subsequently
analyzed for monosaccharide content by any suitable analytical
technique (e.g., HPLC, MS, GC, pH detection, or the like with or
without chemical or enzymatic derivatization before detection).
This method can be used to detect MPS IIIC disease, measure disease
severity, or to measure response to therapy.
[0215] As discussed above, in certain embodiments, using the method
described herein, MPS IIIC is diagnosed in an individual from a
biological sample taken therefrom. For example, in some
embodiments, a biological sample is optionally placed in to a
defined MW cut off spin column (retains large molecules when spun),
optionally washed (e.g., with 1 or more volumes of water or buffer
to remove free glucosamine and/or N-acetyl glucosamine), and
treated with a glucosamine N-acetyltransferase followed by a
hexosaminidase (e.g., to liberate a glycan residual compound
N-acetyl glucosamine). In some embodiments, after incubation, the
liberated N-acetyl glucosamine is optionally isolated by washing
the free N-acetyl glucosamine (e.g., through a defined MW cut off
membrane or by any other suitable method). In some of such
embodiments, the free N-acetyl glucosamine for detection and/or
quantitation is present in the flow through. In certain
embodiments, the resulting isolated solution is optionally dried or
otherwise treated to concentrate the sample and subsequently
analyzed for monosaccharide content by any suitable analytical
technique (e.g., HPLC, MS, GC, pH detection, or the like with or
without chemical or enzymatic derivatization before detection).
This method can be used to detect MPS IIIC disease, measure disease
severity, or to measure response to therapy.
[0216] MPS IIID is a human genetic disease caused by a deficiency
in the enzyme glucosamine 6-O sulfatase. This enzyme is required in
the lysosome to degrade glycans that contain 6-O-sulfated
glucosamine residues. Due to this enzymatic deficiency, glycans
with a 6-O-sulfated N-acetyl glucosamine residue on the
non-reducing end accumulate to high levels (including heparan
sulfate). In certain embodiments, using the method described
herein, MPS IIIC is diagnosed in an individual from a biological
sample taken therefrom. For example, in some embodiments, a
biological sample is optionally placed in to a defined MW cut off
spin column (retains large molecules when spun), optionally washed
(e.g., with 1 or more volumes of water or buffer to remove free
sulfate), and treated with a 6-O-sulfatase (e.g., to liberate a
glycan residual compound sulfate). In some embodiments, after
incubation, the liberated sulfate is optionally isolated by washing
the free sulfate (e.g., through a defined MW cut off membrane or by
any other suitable method). In some of such embodiments, the free
sulfate for detection and/or quantitation is present in the flow
through. In certain embodiments, the resulting isolated solution is
optionally dried or otherwise treated to concentrate the sample and
subsequently analyzed for sulfate content by any suitable
analytical technique (e.g., HPLC, MS, GC, pH detection, or the like
with or without chemical or enzymatic derivatization before
detection). This method can be used to detect MPS IIID disease,
measure disease severity, or to measure response to therapy.
[0217] As discussed above, in certain embodiments, using the method
described herein, MPS IIID is diagnosed in an individual from a
biological sample taken therefrom. For example, in some
embodiments, a biological sample is optionally placed in to a
defined MW cut off spin column (retains large molecules when spun),
optionally washed (e.g., with 1 or more volumes of water or buffer
to remove free sulfate and/or N-acetyl glucosamine), and treated
with a 6-O-sulfatase and a hexosaminidase (e.g., to liberate a
glycan residual compound N-acetyl glucosamine). In some
embodiments, after incubation, the liberated N-acetyl glucosamine
is optionally isolated by washing the free N-acetyl glucosamine
(e.g., through a defined MW cut off membrane or by any other
suitable method). In some of such embodiments, the free
monosaccharide for detection and/or quantitation is present in the
flow through. In certain embodiments, the resulting isolated
solution is optionally dried or otherwise treated to concentrate
the sample and subsequently analyzed for monosaccharide content by
any suitable analytical technique (e.g., HPLC, MS, GC, or the like
with or without chemical or enzymatic derivatization before
detection). This method can be used to detect MPS IIID disease,
measure disease severity, or to measure response to therapy.
[0218] As discussed above, in certain embodiments, using the method
described herein, MPS IIID is diagnosed in an individual from a
biological sample taken therefrom. For example, in some
embodiments, a biological sample is optionally placed in to a
defined MW cut off spin column (retains large molecules when spun),
optionally washed (e.g., with 1 or more volumes of water or buffer
to remove free sulfate and/or N-acetyl glucosamine 6-O sulfate),
and treated with a hexosaminidase or heparin lyase (e.g., to
liberate a glycan residual compound N-acetyl glucosamine 6-O
sulfate). In some embodiments, after incubation, the liberated
N-acetyl glucosamine 6-O sulfate is optionally isolated by washing
the free N-acetyl glucosamine 6-O sulfate (e.g., through a defined
MW cut off membrane or by any other suitable method). In some of
such embodiments, the free monosaccharide for detection and/or
quantitation is present in the flow through. In certain
embodiments, the resulting isolated solution is optionally dried or
otherwise treated to concentrate the sample and subsequently
analyzed for monosaccharide content by any suitable analytical
technique (e.g., HPLC, MS, GC, pH detection, or the like with or
without chemical or enzymatic derivatization before detection).
This method can be used to detect MPS IIID disease, measure disease
severity, or to measure response to therapy.
[0219] MPS IVA is a human genetic disease caused by a deficiency in
the enzyme lysosomal enzyme galactose/N-acetyl galactosamine 6-O
sulfatase. This enzyme is required in the lysosome to degrade
glycans that contain 6-O-sulfated galactose and 6-O sulfated
N-acetyl galactosamine residues. Due to this enzymatic deficiency,
glycans with 6-O-sulfated galactose and 6-O sulfated N-acetyl
galactosamine residues on the non-reducing end accumulate to high
levels (including chondroitin and keratan sulfate). In certain
embodiments, using the method described herein, MPS IVA is
diagnosed in an individual from a biological sample taken
therefrom. For example, in some embodiments, a biological sample is
optionally placed in to a defined MW cut off spin column (retains
large molecules when spun), optionally washed (e.g., with 1 or more
volumes of water or buffer to remove free monosaccharide), and
treated with a galactose 6-O-sulfatase and/or an N-acetyl
galactosamine 6-O sulfatase and a galactosidase and/or
hexosaminidase (e.g., to liberate a glycan residual compound Gal
and/or GalNAc). In some embodiments, after incubation, the
liberated monosaccharide is optionally isolated by washing the free
monosaccharide (e.g., through a defined MW cut off membrane or by
any other suitable method). In some of such embodiments, the free
monosaccharide for detection and/or quantitation is present in the
flow through. In certain embodiments, the resulting isolated
solution is optionally dried or otherwise treated to concentrate
the sample and subsequently analyzed for monosaccharide content by
any suitable analytical technique (e.g., HPLC, MS, GC, or the like
with or without chemical or enzymatic derivatization before
detection). This method can be used to detect MPS IVA disease,
measure disease severity, or to measure response to therapy.
[0220] As discussed above, in certain embodiments, using the method
described herein, MPS IVA is diagnosed in an individual from a
biological sample taken therefrom. For example, in some
embodiments, a biological sample is optionally placed in to a
defined MW cut off spin column (retains large molecules when spun),
optionally washed (e.g., with 1 or more volumes of water or buffer
to remove free sulfate), and treated with a 6-O-sulfatase capable
of desulfating 6-O-sulfated galactose and/or 6-O sulfated N-acetyl
galactosamine residues (e.g., to liberate a glycan residual
compound sulfate). In some embodiments, after incubation, the
liberated sulfate is optionally isolated by washing the free
sulfate (e.g., through a defined MW cut off membrane or by any
other suitable method). In some of such embodiments, the free
sulfate for detection and/or quantitation is present in the flow
through. In certain embodiments, the resulting isolated solution is
optionally dried or otherwise treated to concentrate the sample and
subsequently analyzed for sulfate content by any suitable
analytical technique (e.g., HPLC, MS, GC, pH detection, or the like
with or without chemical or enzymatic derivatization before
detection). This method can be used to detect MPS IVA disease,
measure disease severity, or to measure response to therapy.
[0221] MPS IVB is a human genetic disease caused by a deficiency in
the enzyme lysosomal .beta.-galactosidase. This enzyme is required
in the lysosome to degrade glycans that contain galactose residues.
Due to this enzymatic deficiency, glycans with .beta.-galactose
residues on the non-reducing end accumulate to high levels
(including keratan sulfate and other glycans). In certain
embodiments, using the method described herein, MPS IVB is
diagnosed in an individual from a biological sample taken
therefrom. For example, in some embodiments, a biological sample is
optionally placed in to a defined MW cut off spin column (retains
large molecules when spun), optionally washed (e.g., with 1 or more
volumes of water or buffer to remove free monosaccharide), and
treated with a galactosidase (e.g., to liberate a glycan residual
compound Gal). In some embodiments, after incubation, the liberated
monosaccharide is optionally isolated by washing the free
monosaccharide (e.g., through a defined MW cut off membrane or by
any other suitable method). In some of such embodiments, the free
monosaccharide for detection and/or quantitation is present in the
flow through. In certain embodiments, the resulting isolated
solution is optionally dried or otherwise treated to concentrate
the sample and subsequently analyzed for monosaccharide content by
any suitable analytical technique (e.g., HPLC, MS, GC, or the like
with or without chemical or enzymatic derivatization before
detection). This method can be used to detect MPS IVB disease,
measure disease severity, or to measure response to therapy.
[0222] MPS VI is a human genetic disease caused by a deficiency in
the enzyme 4-O sulfatase that desulfates N-acetyl galactosamine.
This enzyme is required in the lysosome to degrade glycans that
contain 4-O-sulfated N-acetyl galactosamine residues. Due to this
enzymatic deficiency, glycans with 4-O-sulfated N-acetyl
galactosamine residues on the non-reducing end accumulate to high
levels (including chondroitin sulfate). In certain embodiments,
using the method described herein, MPS VI is diagnosed in an
individual from a biological sample taken therefrom. For example,
in some embodiments, a biological sample is optionally placed in to
a defined MW cut off spin column (retains large molecules when
spun), optionally washed (e.g., with 1 or more volumes of water or
buffer to remove free sulfate), and treated with a 4-O-sulfatase
that can desulfate 4-O-sulfated N-acetyl galactosamine residues
(e.g., to liberate a glycan residual compound sulfate). In some
embodiments, after incubation, the liberated sulfate is optionally
isolated by washing the free sulfate (e.g., through a defined MW
cut off membrane or by any other suitable method). In some of such
embodiments, the free sulfate for detection and/or quantitation is
present in the flow through. In certain embodiments, the resulting
isolated solution is optionally dried or otherwise treated to
concentrate the sample and subsequently analyzed for sulfate
content by any suitable analytical technique (e.g., HPLC, MS, GC,
pH detection, or the like with or without chemical or enzymatic
derivatization before detection). This method can be used to detect
MPS VI disease, measure disease severity, or to measure response to
therapy.
[0223] As discussed above, in certain embodiments, using the method
described herein, MPS VI is diagnosed in an individual from a
biological sample taken therefrom. For example, in some
embodiments, a biological sample is optionally placed in to a
defined MW cut off spin column (retains large molecules when spun),
optionally washed (e.g., with 1 or more volumes of water or buffer
to remove free N-acetyl galactosamine), and treated with a
4-O-sulfatase that is capable of desulfating 4-O-sulfated N-acetyl
galactosamine residues then treated with a hexosaminidase (e.g., to
liberate a glycan residual compound N-acetyl galactosamine). In
some embodiments, after incubation, the liberated N-acetyl
galactosamine is optionally isolated by washing the free
monosaccharide (e.g., through a defined MW cut off membrane or by
any other suitable method). In some of such embodiments, the free
monosaccharide for detection and/or quantitation is present in the
flow through. In certain embodiments, the resulting isolated
solution is optionally dried or otherwise treated to concentrate
the sample and subsequently analyzed for monosaccharide content by
any suitable analytical technique (e.g., HPLC, MS, GC, or the like
with or without chemical or enzymatic derivatization before
detection). This method can be used to detect MPS VI disease,
measure disease severity, or to measure response to therapy.
[0224] MPS VII is a human genetic disease caused by a deficiency in
the lysosomal enzyme beta-glucuronidase. This enzyme is required in
the lysosome to degrade glycans that contain glucuronic acid
residues. Due to this enzymatic deficiency, glycans with glucuronic
acid residues on the non-reducing end accumulate to high levels
(including chondroitin sulfate, heparan sulfate and others). In
certain embodiments, using the method described herein, MPS VII is
diagnosed in an individual from a biological sample taken
therefrom. For example, in some embodiments, a biological sample is
optionally placed in to a defined MW cut off spin column (retains
large molecules when spun), optionally washed (e.g., with 1 or more
volumes of water or buffer to remove free glucuronic acid), and
treated with a glucuronidase (e.g., to liberate a glycan residual
compound glucuronic acid). In some embodiments, after incubation,
the liberated monosaccharide is optionally isolated by washing the
free monosaccharide (e.g., through a defined MW cut off membrane or
by any other suitable method). In some of such embodiments, the
free monosaccharide for detection and/or quantitation is present in
the flow through. In certain embodiments, the resulting isolated
solution is optionally dried or otherwise treated to concentrate
the sample and subsequently analyzed for monosaccharide content by
any suitable analytical technique (e.g., HPLC, MS, GC, pH
detection, or the like with or without chemical or enzymatic
derivatization before detection). This method can be used to detect
MPS VII disease, measure disease severity, or to measure response
to therapy.
[0225] Methods described herein can also be used to define the
relative presence of different glycan classes.
[0226] Fabry Disease is a human genetic disease caused by a
deficiency in the lysosomal .alpha.-galactosidase. Due to this
enzymatic deficiency, glycans with non-reducing end terminal
.alpha.-galactose residues are abundant. In certain embodiments,
using the method described herein, Fabry Disease is diagnosed in an
individual from a biological sample taken therefrom. For example,
in some embodiments, a biological sample is optionally placed in to
a defined MW cut off spin column (retains large molecules when
spun), optionally washed (e.g., with 1 or more volumes of water or
buffer to remove free monosaccharide), and treated with a
galactosidase that is capable of liberating a non-reducing end
monosaccharide (e.g., to liberate a glycan residual compound). In
some embodiments, after incubation, the liberated glycan residual
compound is optionally isolated by washing the free glycan residual
compound (e.g., through a defined MW cut off membrane or by any
other suitable method). In some of such embodiments, the free
glycan residual compound for detection and/or quantitation is
present in the flow through. In certain embodiments, the resulting
isolated solution is optionally dried or otherwise treated to
concentrate the sample and subsequently analyzed for glycan
residual compound content by any suitable analytical technique
(e.g., HPLC, MS, GC, pH detection, or the like with or without
chemical or enzymatic derivatization before detection). This method
can be used to detect Fabry Disease, measure disease severity, or
to measure response to therapy.
[0227] In some embodiments, as described in Table 1, other enzymes
and processes are optionally utilized to diagnose other lysosomal
storage diseases (LSDs). As described in the table, the appropriate
enzyme(s) can be selected as appropriate for the specific
disease.
Oncology--Melanoma and Neuroblastoma Via Sialic Acid
[0228] A hallmark of cancer is altered glycosylation. The changes
in glycosylation are a reflection of changes in enzymes and factors
that regulate the biosynthesis, turnover, presentation, stability,
solubility, and degradation of glycans. Many of these changes
result in glycans being produced that have altered structures. The
methods described here are utilized in various embodiments to
evaluate those structural changes (e.g., measure abnormal glycan
accumulation) that are present on the non-reducing end of the
glycans present in individuals suffering from a cancerous
disease.
[0229] Some examples of cancerous diseases suitable for diagnosis
and/or monitoring therapy according to methods described herein
include, by way of non-limiting example, melanoma and
neuroblastoma. In some instances, such cancers have alterations in
the biosynthesis, turnover, presentation, stability, solubility, or
degradation of gangliosides. In some instances, these sialic acid
modified glycolipids are detected and/or otherwise characterized or
analyzed in a biological sample (e.g., serum) of patients with
these tumor types. In some embodiments, the abundance of the
heterogeneous population of gangliosides is quantified to measuring
sialic acid or other glycan residual released from gangliosides in
the blood.
[0230] Due to this enzymatic alteration, gangliosides and other
glycans are present in the body at high levels. In certain
embodiments, using the method described herein, cancer (e.g.,
melanoma or neuroblastoma) is diagnosed in an individual from a
biological sample taken therefrom. For example, in some
embodiments, a biological sample is optionally placed in to a
defined MW cut off spin column (retains large molecules when spun),
optionally washed (e.g., with 1 or more volumes of water or buffer
to remove free sialic acid), and treated with a sialidase that can
liberate sialic acid (e.g., to liberate a glycan residual compound
sialic acid). In some embodiments, after incubation, the liberated
sialic acid is optionally isolated by washing the free sialic acid
(e.g., through a defined MW cut off membrane or by any other
suitable method). In some of such embodiments, the free sialic acid
for detection and/or quantitation is present in the flow through.
In certain embodiments, the resulting isolated solution is
optionally dried or otherwise treated to concentrate the sample and
subsequently analyzed for sialic acid content by any suitable
analytical technique (e.g., HPLC, MS, GC, pH detection, or the like
with or without chemical or enzymatic derivatization before
detection). This method can be used to detect cancer (e.g.,
melanoma or neuroblastoma) disease, measure disease severity, or to
measure response to therapy.
Oncology--Myeloma Via Heparan Sulfate Nonreducing Ends
[0231] An example of a human cancer that is diagnosed and/or
monitored according to the methods described herein (i.e., by
analyzing with such a method the altered degradation of a glycan)
is multiple myeloma. In certain instances, multiple myeloma
commonly produces heparanase. Heparanase is an endoglycosidase that
cleaved heparan sulfate into smaller fragments, exposing novel
non-reducing end structures. In certain embodiments described
herein, the presence of these novel non-reducing end structures are
detected using any method described herein (e.g., by incubating a
biological sample with various glycosidases or sulfatases to detect
the presence of novel glycan non-reducing ends).
[0232] Due to this enzymatic alteration, glycans (including heparan
sulfate and others) are present in the body at high levels. In
certain embodiments, using the method described herein, cancer
(e.g., multiple myeloma) is diagnosed in an individual from a
biological sample taken therefrom. For example, in some
embodiments, a biological sample is optionally placed in to a
defined MW cut off spin column (retains large molecules when spun),
optionally washed (e.g., with 1 or more volumes of water or buffer
to remove free monosaccharides and/or sulfate), and treated with a
sulfatase, iduronidase, glucuronidase, hexosaminidase, or lyase
that is capable of liberating a non-reducing end monosaccharide or
sulfate. In some embodiments, after incubation, the liberated
glycan residual compound is optionally isolated by washing the free
glycan residual compound (e.g., through a defined MW cut off
membrane or by any other suitable method). In some of such
embodiments, the free glycan residual compound for detection and/or
quantitation is present in the flow through. In certain
embodiments, the resulting isolated solution is optionally dried or
otherwise treated to concentrate the sample and subsequently
analyzed for glycan residual compound content by any suitable
analytical technique (e.g., HPLC, MS, GC, pH detection, or the like
with or without chemical or enzymatic derivatization before
detection). This method can be used to detect cancer (e.g.,
multiple myeloma) disease, measure disease severity, or to measure
response to therapy.
Oncology--Adenocarcinoma
[0233] Adenocarcinoma is associated with changes in glycosylation
including increased sialylation and fucosylation. The described
method can be used to measure disease by analyzing glycans (total
or purified or enriched for specific glycan classes) from a patient
for the amount of nonreducing end terminal sialic acid or fucose,
by measuring the release of these glycan residuals after treatment
with a sialidase or fucosidase.
Other Applications
[0234] As described in Tables 12-15, various diseases associated
with changes in glycosylation are optionally diagnosed and/or
monitored according to methods described herein. Various disorders
include, by way of non-limiting example, lysosomal storage disease,
cancer, neurological disease (dementia, Alzheimer's, etc), liver
disease, bone disease, infectious diseases, and the like.
[0235] Provided herein are methods of diagnosing individuals
(including, e.g., a disease state or the severity of a disease
states) with a lysosomal storage disease (LSD) or methods of
monitoring the treatment of a lysosomal storage disease (LSD).
Provided in Table 10 are specific embodiments of disease that are
optionally diagnosed and/or monitored according to various
embodiments described herein. Table 12 also illustrates various
non-limiting embodiments of specific enzyme(s) that are optionally
utilized to treat a biological sample from an individual suffering
from or suspected (e.g., through a pre- or preliminary screening
process) of suffering from an LSD. Moreover, Table 12 further
illustrates various glycan residual compounds that are liberated in
various embodiments described herein, such liberated glycan
residual compounds optionally being detected and/or measured in
order to diagnose and/or monitor a lysosomal storage disease
(LSD).
TABLE-US-00012 TABLE 12 Exemplary LSD Uses Primary Secondary Glycan
Non-Reducing Releasing Releasing Residual Disease End Structure
Enzyme Enzyme Compound MPS I IdoA iduronidase IdoA MPS II IdoA-2-O
sufate 2-sulfatase Sulfate and GlcA-2-O sufate MPS II IdoA-2-O
sufate 2-sulfatase Iduronidase IdoA and/or and GlcA-2-O and/or GlcA
sufate glucuronidase MPS IIIA GlcN-N-sulfate N-sulfatase Sulfate
MPS IIIA GlcN-N-sulfate N-sulfatase hexosaminidase GlcN MPS IIIA
GlcN-N-sulfate N-sulfatase Heparin lyase GlcN MPS IIIA
GlcN-N-sulfate N-sulfatase N-acetyl GlcNAc transferase and
hexosaminidase MPS IIIA GlcN-N-sulfate Heparin lyase GlcN-N-sulfate
MPS IIIB GlcNAc hexosaminidase GlcNAc MPS IIIB GlcNAc Deacetylase
acetate MPS IIIB GlcNAc Heparin lyase GlcNAc MPS IIIC GlcNAc-6-O
6-O sulfatase Sulfate sulfate MPS IIIC GlcNAc-6-O 6-O sulfatase
hexosaminidase GlcNAc sulfate MPS IIIC GlcNAc-6-O 6-O sulfatase
Heparin lyase GlcNAc sulfate MPS IIIC GlcNAc-6-O Heparin lyase
GlcNAc-6-O sulfate sulfate MPS IIID GlcN hexosaminidase GlcN MPS
IIID GlcN Heparin lyase GlcN MPS IIID GlcN N-acetyl hexosaminidase
GlcNAc transferase MPS IVA Gal-6-O sulfate 6-O sulfatase Sulfate
and GalNAc-6-O sulfate MPS IVA Gal-6-O sulfate galactosidase
Gal-6-O sulfate and GalNAc-6-O sulfate MPS IVA Gal-6-O sulfate
N-acetyl GalNAc-6-O and GalNAc-6-O galactosidase sulfate sulfate
MPS IVA Gal-6-O sulfate hexosaminidase GalNAc-6-O and GalNAc-6-O
sulfate sulfate MPS IVA Gal-6-O sulfate 6-O sulfatase galactosidase
Gal and GalNAc-6-O sulfate MPS IVA Gal-6-O sulfate 6-O sulfatase
N-acetyl GalNAc and GalNAc-6-O galactosidase sulfate MPS IVA
Gal-6-O sulfate Any GalNAc-6-O and GalNAc-6-O combination of
sulfate (+/-4-O sulfate (+/-4-O- Chondroitin sulfate) sulfate)
lyase A and/or B and/or C activities) MPS IVA Gal-6-O sulfate 6-O
sulfatase Any GalNAc (+/-4- and GalNAc-6-O combination of O
sulfate) sulfate (+/-4-O- Chondroitin sulfate) lyase A and/or B
and/or C activities) MPS IVB Gal Galactosidase Gal MPS VI
GalNAc-4-O 4-O sulfatase Sulfate sulfate MPS VI GalNAc-4-O 4-O
sulfatase hexosaminidase GalNAc sulfate MPS VI GalNAc-4-O 4-O
sulfatase Chondroitin GalNAc sulfate lyase MPS VI GalNAc-4-O
Chondroitin GalNAc-4-O sulfate lyase sulfate MPS VII GlcA .beta.-
GlcA glucuronidase Alpha Mannosidosis Mannose Manosidase Man
Aspartylglucosaminuria GlcNAc hexosaminidase GlcNAc Fabry Galactose
galactosidase Gal Fucosidosis Fucose fucosidase Fuc
Galactosialidosis Galactose and/or Galactosidase Gal and/or Sialic
acid and/or sialidase Sialic acid Gaucher glucose glucosidase
glucose GM1 gangliosidosis Beta-Galactose Beta- galactose
Galactosidase GM1 gangliosidosis Beta-Galactose Beta-
Hexosaminidase GalNAc Galactosidase GM2 activator GalNAc
hexosaminidase GalNAc deficiency Sialidosis Sialic acid Sialidase
Sialic acid Sialidosis Sialic acid Alpha 2,3 Sialic acid Sialidase
Sialidosis Sialic acid Alphas 2,6 Sialic acid Sialidase Sialidosis
Sialic acid Alphas 2,8 Sialic acid Sialidase Krabbe Galactose
galactosidase Galactose Metachromatic Sulfated 3-O sulfatase
Sulfate Leukodystrophy galactosylceramide Metachromatic Sulfated
3-O sulfatase galactosidase Galactose Leukodystrophy
galactosylceramide Mucolipidosis II Broad range of Any listed Any
glycans enzyme monosaccharide or sulfate Mucolipidosis III Broad
range of Any listed Any glycans enzyme monosaccharide or sulfate
Mucolipidosis IV Broad range of Any listed Any glycans enzyme
monosaccharide or sulfate Multiple Sulfatase Sulfated glycans
sulfatase sulfate Deficiency Multiple Sulfatase Sulfated glycans
sulfatase Any monosaccharide Deficiency glycosidase Multiple
Sulfatase Sulfated glycans Any Sulfated Deficiency glycosidase
monosaccharide Glycogen Storage glucose glucosidase glucose Disease
(Pompe) Sandhoff GalNAc hexosaminidase GalNAc Tay-Sachs GalNAc
hexosaminidase GalNAc AB Variant GalNAc hexosaminidase GalNAc
Schindler Disease Alpha-GalNAc hexosaminidase GalNAc Salla Disease
Sialic acid none Sialic Acid Alpha Mannosidosis Alpha mannose
mannosidase Mannose Beta Mannosidosis Beta mannose mannosidase
Mannose Globoid cell galactose galactosidase galactose
leukodystrophy
[0236] Provided herein are methods of diagnosing individuals
(including, e.g., a disease state or the severity of a disease
states) with a cancerous disease state or methods of monitoring the
treatment of a cancer. Provided in Table 13 are specific
embodiments of disease that are optionally diagnosed and/or
monitored according to various embodiments described herein. Table
13 also illustrates various non-limiting embodiments of specific
enzyme(s) that are optionally utilized to treat a biological sample
from an individual suffering from or suspected of (e.g., through a
pre- or preliminary screening process) suffering from a cancerous
disease state. Moreover, Table 13 further illustrates various
glycan residual compounds that are liberated in various embodiments
described herein, such liberated glycan residual compounds
optionally being detected and/or measured in order to diagnose
and/or monitor a cancerous disease state.
TABLE-US-00013 TABLE 13 Exemplary Oncology Uses Non- Glycan
Reducing Primary Secondary Residual End Liberating Liberating Com-
Cancer Type Structure Enzyme Enzyme pound Melanoma Sialic Sialidase
Sialic Acid acid Melanoma Sialic Alpha 2,8 Sialic Acid Sialidase
acid Melanoma Sialic Alpha 2,3 Sialic Acid Sialidase acid Melanoma
Sialic Alpha 2,6 Sialic Acid Sialidase acid Melanoma GalNAc Hexos-
GalNAc aminidase Melanoma GalNAc Sialidase Hexos- GalNAc aminidase
Melanoma Sialic Hexos- Sialidase Sialic Acid aminidase acid
Melanoma Galactose galactosidase Galactose Melanoma Galactose
sialidase galactosidase Galactose Melanoma Fucose fucosidase Fucose
Melanoma Galactose Galactosidase Galactose Melanoma GlcNAc hexos-
GlcNAc aminidase Melanoma Sulfate Sulfatase Sulfate Melanoma
Sulfated Sulfatase hexos- GlcNAc hexose aminidase or GalNAc
Melanoma Sulfated Sulfatase Iduronidase or IdoA or uronic
glucouronidase GlcA acid Neuroblastoma Sialic Sialidase Sialic Acid
acid Neuroblastoma Sialic Alpha 2,8 Sialic Acid Sialidase acid
Neuroblastoma Sialic Alpha 2,3 Sialic Acid Sialidase acid
Neuroblastoma Sialic Alpha 2,6 Sialic Acid Sialidase acid
Neuroblastoma GalNAc Hexos- GalNAc aminidase Neuroblastoma GalNAc
Sialidase Hexos- GalNAc aminidase Neuroblastoma Sialic Hexos-
Sialidase Sialic acid aminidase acid Neuroblastoma Galactose
galactosidase Galactose Neuroblastoma Galactose sialidase
galactosidase Galactose Neuroblastoma Fucose fucosidase Fucose
Neuroblastoma Galactose Galactosidase Galactose Neuroblastoma
GlcNAc hexos- GlcNAc aminidase Neuroblastoma Sulfate Sulfatase
Sulfate Neuroblastoma Sulfated Sulfatase hexos- GlcNAc hexose
aminidase or GalNAc Neuroblastoma Sulfated Sulfatase Iduronidase or
IdoA or uronic glucouronidase GlcA acid Adenocarcinoma Sialic
Sialidase Sialic Acid acid Adenocarcinoma Sialic Alpha 2,8 Sialic
Acid Sialidase acid Adenocarcinoma Sialic Alpha 2,3 Sialic Acid
Sialidase acid Adenocarcinoma Sialic Alpha 2,6 Sialic Acid
Sialidase acid Adenocarcinoma GalNAc Hexos- GalNAc aminidase
Adenocarcinoma GalNAc Sialidase Hexos- GalNAc aminidase
Adenocarcinoma Sialic Hexos- Sialidase Sialic Acid aminidase acid
Adenocarcinoma Galactose galactosidase Galactose Adenocarcinoma
Galactose sialidase galactosidase Galactose Adenocarcinoma Fucose
fucosidase Fucose Adenocarcinoma Galactose Galactosidase Galactose
Adenocarcinoma GlcNAc hexos- GlcNAc aminidase Adenocarcinoma
Sulfate Sulfatase Sulfate Adenocarcinoma Sulfated Sulfatase hexos-
GlcNAc hexose aminidase or GalNAc Adenocarcinoma Sulfated Sulfatase
Iduronidase or IdoA or uronic glucouronidase GlcA acid Myeloma
Sialic Sialidase Sialic Acid acid Myeloma Sialic Alpha 2,8 Sialic
Acid Sialidase acid Myeloma Sialic Alpha 2,3 Sialic Acid Sialidase
acid Myeloma Sialic Alpha 2,6 Sialic Acid Sialidase acid Myeloma
GalNAc Hexos- GalNAc aminidase Myeloma GalNAc Sialidase Hexos-
GalNAc aminidase Myeloma Sialic Hexos- Sialidase Sialic acid
aminidase acid Myeloma Galactose galactosidase Galactose Myeloma
Galactose sialidase galactosidase Galactose Myeloma Fucose
fucosidase Fucose Myeloma Galactose Galactosidase Galactose Myeloma
GlcNAc hexos- GlcNAc aminidase Myeloma Sulfate Sulfatase Sulfate
Myeloma Sulfated Sulfatase hexos- GlcNAc hexose aminidase or GalNAc
Myeloma Sulfated Sulfatase Iduronidase or IdoA or uronic
glucouronidase GlcA acid Breast Sialic Sialidase Sialic Acid acid
Breast Sialic Alpha 2,8 Sialic Acid Sialidase acid Breast Sialic
Alpha 2,3 Sialic Acid Sialidase acid Breast Sialic Alpha 2,6 Sialic
Acid Sialidase acid Breast GalNAc Hexos- GalNAc aminidase Breast
GalNAc Sialidase Hexos- GalNAc aminidase Breast Sialic Hexos-
Sialidase Sialic acid aminidase acid Breast Galactose galactosidase
Galactose Breast Galactose sialidase galactosidase Galactose Breast
Fucose fucosidase Fucose Breast Galactose Galactosidase Galactose
Breast GlcNAc hexos- GlcNAc aminidase Breast Sulfate Sulfatase
Sulfate Breast Sulfated Sulfatase hexos- GlcNAc hexose aminidase or
GalNAc Breast Sulfated Sulfatase Iduronidase or IdoA or uronic
glucouronidase GlcA acid Ovarian Sialic Sialidase Sialic Acid acid
Ovarian Sialic Alpha 2,8 Sialic Acid Sialidase acid Ovarian Sialic
Alpha 2,3 Sialic Acid Sialidase acid Ovarian Sialic Alpha 2,6
Sialic Acid Sialidase acid Ovarian GalNAc Hexos- GalNAc aminidase
Ovarian GalNAc Sialidase Hexos- GalNAc aminidase Ovarian Sialic
Hexos- Sialidase Sialic acid aminidase acid Ovarian Galactose
galactosidase Galactose Ovarian Galactose sialidase galactosidase
Galactose Ovarian Fucose fucosidase Fucose Ovarian Galactose
Galactosidase Galactose Ovarian GlcNAc hexos- GlcNAc aminidase
Ovarian Sulfate Sulfatase Sulfate Ovarian Sulfated Sulfatase hexos-
GlcNAc hexose aminidase or GalNAc Ovarian Sulfated Sulfatase
Iduronidase or IdoA or uronic glucouronidase GlcA acid Stomach
Sialic Sialidase Sialic Acid acid Stomach Sialic Alpha 2,8 Sialic
Acid Sialidase acid Stomach Sialic Alpha 2,3 Sialic Acid Sialidase
acid Stomach Sialic Alpha 2,6 Sialic Acid Sialidase acid Stomach
GalNAc Hexos- GalNAc aminidase Stomach GalNAc Sialidase Hexos-
GalNAc aminidase Stomach Sialic Hexos- Sialidase Sialic acid
aminidase acid Stomach Galactose galactosidase Galactose Stomach
Galactose sialidase galactosidase Galactose Stomach Fucose
fucosidase Fucose Stomach Galactose Galactosidase Galactose Stomach
GlcNAc hexos- GlcNAc aminidase Stomach Sulfate Sulfatase Sulfate
Stomach Sulfated Sulfatase hexos- GlcNAc hexose aminidase or GalNAc
Stomach Sulfated Sulfatase Iduronidase or IdoA or uronic
glucouronidase GlcA acid Lung Sialic Sialidase Sialic Acid acid
Lung Sialic Alpha 2,8 Sialic Acid Sialidase acid Lung Sialic Alpha
2,3 Sialic Acid Sialidase acid Lung Sialic Alpha 2,6 Sialic Acid
Sialidase acid Lung GalNAc Hexos- GalNAc aminidase Lung GalNAc
Sialidase Hexos- GalNAc aminidase Lung Sialic Hexos- Sialidase
Sialic acid aminidase acid Lung Galactose galactosidase Galactose
Lung Galactose sialidase galactosidase Galactose Lung Fucose
fucosidase Fucose Lung Galactose Galactosidase Galactose Lung
GlcNAc hexos- GlcNAc aminidase Lung Sulfate Sulfatase Sulfate Lung
Sulfated Sulfatase hexos- GlcNAc hexose aminidase or GalNAc Lung
Sulfated Sulfatase Iduronidase or IdoA or uronic glucouronidase
GlcA acid Pancreatic Sialic Sialidase Sialic Acid acid Pancreatic
Sialic Alpha 2,8 Sialic Acid Sialidase acid Pancreatic Sialic Alpha
2,3 Sialic Acid Sialidase acid Pancreatic Sialic Alpha 2,6 Sialic
Acid Sialidase acid Pancreatic GalNAc Hexos- GalNAc aminidase
Pancreatic GalNAc Sialidase Hexos- GalNAc aminidase Pancreatic
Sialic Hexos- Sialidase Sialic acid aminidase acid Pancreatic
Galactose galactosidase Galactose Pancreatic Galactose sialidase
galactosidase Galactose Pancreatic Fucose fucosidase Fucose
Pancreatic Galactose Galactosidase Galactose Pancreatic GlcNAc
hexos- GlcNAc aminidase Pancreatic Sulfate Sulfatase Sulfate
Pancreatic Sulfated Sulfatase hexos- GlcNAc hexose aminidase or
GalNAc Pancreatic Sulfated Sulfatase Iduronidase or IdoA or uronic
glucouronidase GlcA
acid Oral Sialic Sialidase Sialic Acid acid Oral Sialic Alpha 2,8
Sialic Acid Sialidase acid Oral Sialic Alpha 2,3 Sialic Acid
Sialidase acid Oral Sialic Alpha 2,6 Sialic Acid Sialidase acid
Oral GalNAc Hexos- GalNAc aminidase Oral GalNAc Sialidase Hexos-
GalNAc aminidase Oral Sialic Hexos- Sialidase Sialic acid aminidase
acid Oral Galactose galactosidase Galactose Oral Galactose
sialidase galactosidase Galactose Oral Fucose fucosidase Fucose
Oral Galactose Galactosidase Galactose Oral GlcNAc hexos- GlcNAc
aminidase Oral Sulfate Sulfatase Sulfate Oral Sulfated Sulfatase
hexos- GlcNAc hexose aminidase or GalNAc Oral Sulfated Sulfatase
Iduronidase or IdoA or uronic glucouronidase GlcA acid Colorectal
Sialic Sialidase Sialic Acid acid Colorectal Sialic Alpha 2,8
Sialic Acid Sialidase acid Colorectal Sialic Alpha 2,3 Sialic Acid
Sialidase acid Colorectal Sialic Alpha 2,6 Sialic Acid Sialidase
acid Colorectal GalNAc Hexos- GalNAc aminidase Colorectal GalNAc
Sialidase Hexos- GalNAc aminidase Colorectal Sialic Hexos-
Sialidase Sialic acid aminidase acid Colorectal Galactose
galactosidase Galactose Colorectal Galactose sialidase
galactosidase Galactose Colorectal Fucose fucosidase Fucose
Colorectal Galactose Galactosidase Galactose Colorectal GlcNAc
hexos- GlcNAc aminidase Colorectal Sulfate Sulfatase Sulfate
Colorectal Sulfated Sulfatase hexos- GlcNAc hexose aminidase or
GalNAc Colorectal Sulfated Sulfatase Iduronidase or IdoA or uronic
glucouronidase GlcA acid Kidney Sialic Sialidase Sialic Acid acid
Kidney Sialic Alpha 2,8 Sialic Acid Sialidase acid Kidney Sialic
Alpha 2,3 Sialic Acid Sialidase acid Kidney Sialic Alpha 2,6 Sialic
Acid Sialidase acid Kidney GalNAc Hexos- GalNAc aminidase Kidney
GalNAc Sialidase Hexos- GalNAc aminidase Kidney Sialic Hexos-
Sialidase Sialic acid aminidase acid Kidney Galactose galactosidase
Galactose Kidney Galactose sialidase galactosidase Galactose Kidney
Fucose fucosidase Fucose Kidney Galactose Galactosidase Galactose
Kidney GlcNAc hexos- GlcNAc aminidase Kidney Sulfate Sulfatase
Sulfate Kidney Sulfated Sulfatase hexos- GlcNAc hexose aminidase or
GalNAc Kidney Sulfated Sulfatase Iduronidase or IdoA or uronic
glucouronidase GlcA acid Bladder Sialic Sialidase Sialic Acid acid
Bladder Sialic Alpha 2,8 Sialic Acid Sialidase acid Bladder Sialic
Alpha 2,3 Sialic Acid Sialidase acid Bladder Sialic Alpha 2,6
Sialic Acid Sialidase acid Bladder GalNAc Hexos- GalNAc aminidase
Bladder GalNAc Sialidase Hexos- GalNAc aminidase Bladder Sialic
Hexos- Sialidase Sialic acid aminidase acid Bladder Galactose
galactosidase Galactose Bladder Galactose sialidase galactosidase
Galactose Bladder Fucose fucosidase Fucose Bladder Galactose
Galactosidase Galactose Bladder GlcNAc hexos- GlcNAc aminidase
Bladder Sulfate Sulfatase Sulfate Bladder Sulfated Sulfatase hexos-
GlcNAc hexose aminidase or GalNAc Bladder Sulfated Sulfatase
Iduronidase or IdoA or uronic glucouronidase GlcA acid Prostate
Sialic Sialidase Sialic Acid acid Prostate Sialic Alpha 2,8 Sialic
Acid Sialidase acid Prostate Sialic Alpha 2,3 Sialic Acid Sialidase
acid Prostate Sialic Alpha 2,6 Sialic Acid Sialidase acid Prostate
GalNAc Hexos- GalNAc aminidase Prostate GalNAc Sialidase Hexos-
GalNAc aminidase Prostate Sialic Hexos- Sialidase Sialic acid
aminidase acid Prostate Galactose galactosidase Galactose Prostate
Galactose sialidase galactosidase Galactose Prostate Fucose
fucosidase Fucose Prostate Galactose Galactosidase Galactose
Prostate GlcNAc hexos- GlcNAc aminidase Prostate Sulfate Sulfatase
Sulfate Prostate Sulfated Sulfatase hexos- GlcNAc hexose aminidase
or GalNAc Prostate Sulfated Sulfatase Iduronidase or IdoA or uronic
glucouronidase GlcA acid Uterine Sialic Sialidase Sialic Acid acid
Uterine Sialic Alpha 2,8 Sialic Acid Sialidase acid Uterine Sialic
Alpha 2,3 Sialic Acid Sialidase acid Uterine Sialic Alpha 2,6
Sialic Acid Sialidase acid Uterine GalNAc Hexos- GalNAc aminidase
Uterine GalNAc Sialidase Hexos- GalNAc aminidase Uterine Sialic
Hexos- Sialidase Sialic acid aminidase acid Uterine Galactose
galactosidase Galactose Uterine Galactose sialidase galactosidase
Galactose Uterine Fucose fucosidase Fucose Uterine Galactose
Galactosidase Galactose Uterine GlcNAc hexos- GlcNAc aminidase
Uterine Sulfate Sulfatase Sulfate Uterine Sulfated Sulfatase hexos-
GlcNAc hexose aminidase or GalNAc Uterine Sulfated Sulfatase
Iduronidase or IdoA or uronic glucouronidase GlcA acid Thyroid
Sialic Sialidase Sialic Acid acid Thyroid Sialic Alpha 2,8 Sialic
Acid Sialidase acid Thyroid Sialic Alpha 2,3 Sialic Acid Sialidase
acid Thyroid Sialic Alpha 2,6 Sialic Acid Sialidase acid Thyroid
GalNAc Hexos- GalNAc aminidase Thyroid GalNAc Sialidase Hexos-
GalNAc aminidase Thyroid Sialic Hexos- Sialidase Sialic acid
aminidase acid Thyroid Galactose galactosidase Galactose Thyroid
Galactose sialidase galactosidase Galactose Thyroid Fucose
fucosidase Fucose Thyroid Galactose Galactosidase Galactose Thyroid
GlcNAc hexos- GlcNAc aminidase Thyroid Sulfate Sulfatase Sulfate
Thyroid Sulfated Sulfatase hexos- GlcNAc hexose aminidase or GalNAc
Thyroid Sulfated Sulfatase Iduronidase or IdoA or uronic
glucouronidase GlcA acid Liver Sialic Sialidase Sialic Acid acid
Liver Sialic Alpha 2,8 Sialic Acid Sialidase acid Liver Sialic
Alpha 2,3 Sialic Acid Sialidase acid Liver Sialic Alpha 2,6 Sialic
Acid Sialidase acid Liver GalNAc Hexos- GalNAc aminidase Liver
GalNAc Sialidase Hexos- GalNAc aminidase Liver Sialic Hexos-
Sialidase Sialic acid aminidase acid Liver Galactose galactosidase
Galactose Liver Galactose sialidase galactosidase Galactose Liver
Fucose fucosidase Fucose Liver Galactose Galactosidase Galactose
Liver GlcNAc hexos- GlcNAc aminidase Liver Sulfate Sulfatase
Sulfate Liver Sulfated Sulfatase hexos- GlcNAc hexose aminidase or
GalNAc Liver Sulfated Sulfatase Iduronidase or IdoA or uronic
glucouronidase GlcA acid Esophagus Sialic Sialidase Sialic Acid
acid Esophagus Sialic Alpha 2,8 Sialic Acid Sialidase acid
Esophagus Sialic Alpha 2,3 Sialic Acid Sialidase acid Esophagus
Sialic Alpha 2,6 Sialic Acid Sialidase acid Esophagus GalNAc Hexos-
GalNAc aminidase Esophagus GalNAc Sialidase Hexos- GalNAc aminidase
Esophagus Sialic Hexos- Sialidase Sialic acid aminidase acid
Esophagus Galactose galactosidase Galactose Esophagus Galactose
sialidase galactosidase Galactose Esophagus Fucose fucosidase
Fucose Esophagus Galactose Galactosidase Galactose Esophagus GlcNAc
hexos- GlcNAc aminidase Esophagus Sulfate Sulfatase Sulfate
Esophagus Sulfated Sulfatase hexos- GlcNAc hexose aminidase or
GalNAc Esophagus Sulfated Sulfatase Iduronidase or IdoA or uronic
glucouronidase GlcA acid Brain Sialic Sialidase Sialic Acid acid
Brain Sialic Alpha 2,8 Sialic Acid Sialidase acid Brain Sialic
Alpha 2,3 Sialic Acid Sialidase acid Brain Sialic Alpha 2,6
Sialic
Acid Sialidase acid Brain GalNAc Hexos- GalNAc aminidase Brain
GalNAc Sialidase Hexos- GalNAc aminidase Brain Sialic Hexos-
Sialidase Sialic acid aminidase acid Brain Galactose galactosidase
Galactose Brain Galactose sialidase galactosidase Galactose Brain
Fucose fucosidase Fucose Brain Galactose Galactosidase Galactose
Brain GlcNAc hexos- GlcNAc aminidase Brain Sulfate Sulfatase
Sulfate Brain Sulfated Sulfatase hexos- GlcNAc hexose aminidase or
GalNAc Brain Sulfated Sulfatase Iduronidase or IdoA or uronic
glucouronidase GlcA acid Lymphomas Sialic Sialidase Sialic Acid
acid Lymphomas Sialic Alpha 2,8 Sialic Acid Sialidase acid
Lymphomas Sialic Alpha 2,3 Sialic Acid Sialidase acid Lymphomas
Sialic Alpha 2,6 Sialic Acid Sialidase acid Lymphomas GalNAc
Flexos- GalNAc aminidase Lymphomas GalNAc Sialidase Hexos- GalNAc
aminidase Lymphomas Sialic Flexos- Sialidase Sialic acid aminidase
acid Lymphomas Galactose galactosidase Galactose Lymphomas
Galactose sialidase galactosidase Galactose Lymphomas Fucose
fucosidase Fucose Lymphomas Galactose Galactosidase Galactose
Lymphomas GlcNAc hexos- GlcNAc aminidase Lymphomas Sulfate
Sulfatase Sulfate Lymphomas Sulfated Sulfatase hexos- GlcNAc hexose
aminidase or GalNAc Lymphomas Sulfated Sulfatase Iduronidase or
IdoA or uronic glucouronidase GlcA acid Leukemias Sialic Sialidase
Sialic Acid acid Leukemias Sialic Alpha 2,8 Sialic Acid Sialidase
acid Leukemias Sialic Alpha 2,3 Sialic Acid Sialidase acid
Leukemias Sialic Alpha 2,6 Sialic Acid Sialidase acid Leukemias
GalNAc Flexos- GalNAc aminidase Leukemias GalNAc Sialidase Hexos-
GalNAc aminidase Leukemias Sialic Hexos- Sialidase Sialic acid
aminidase acid Leukemias Galactose galactosidase Galactose
Leukemias Galactose sialidase galactosidase Galactose Leukemias
Fucose fucosidase Fucose Leukemias Galactose Galactosidase
Galactose Leukemias GlcNAc hexos- GlcNAc aminidase Leukemias
Sulfate Sulfatase Sulfate Leukemias Sulfated Sulfatase hexos-
GlcNAc hexose aminidase or GalNAc Leukemias Sulfated Sulfatase
Iduronidase or IdoA or uronic glucouronidase GlcA acid
[0237] Provided herein are methods of diagnosing individuals
(including, e.g., a disease state or the severity of a disease
states) with a disease state associated with abnormal glycan
accumulation. Provided in Table 14 are specific embodiments of
disease that are optionally diagnosed and/or monitored according to
various embodiments described herein. Table 14 also illustrates
various non-limiting embodiments of specific enzyme(s) that are
optionally utilized to treat a biological sample from an individual
suffering from or suspected of (e.g., through a pre- or preliminary
screening process) suffering from various disease states associated
with abnormal glycan accumulation. Moreover, Table 14 further
illustrates various glycan residual compounds that are liberated in
various embodiments described herein, such liberated glycan
residual compounds optionally being detected and/or measured in
order to diagnose and/or monitor various disease states.
TABLE-US-00014 TABLE 14 Non- Glycan Reducing Primary Secondary
Residual End Liberating Liberating Com- Disease Structure Enzyme
Enzyme pound Alzheimers Sialic Sialidase Sialic Acid acid
Alzheimers Sialic Alpha 2,8 Sialic Acid Sialidase acid Alzheimers
Sialic Alpha 2,3 Sialic Acid Sialidase acid Alzheimers Sialic Alpha
2,6 Sialic Acid Sialidase acid Alzheimers GalNAc Hexos- GalNAc
aminidase Alzheimers GalNAc Sialidase Hexos- GalNAc aminidase
Alzheimers Sialic Hexos- Sialidase Sialic acid aminidase acid
Alzheimers Galactose galactosidase Galactose Alzheimers Galactose
sialidase galactosidase Galactose Alzheimers Fucose fucosidase
Fucose Alzheimers Galactose Galactosidase Galactose Alzheimers
GlcNAc hexos- GlcNAc aminidase Alzheimers Sulfate Sulfatase Sulfate
Alzheimers Sulfated Sulfatase hexos- GlcNAc hexose aminidase or
GalNAc Alzheimers Sulfated Sulfatase Iduronidase IdoA or uronic or
GlcA acid glucuronidase Amyotrophic Sialic Sialidase Sialic Lateral
Acid acid Sclerosis Amyotrophic Sialic Alpha 2,8 Sialic Lateral
Acid Sialidase acid Sclerosis Amyotrophic Sialic Alpha 2,3 Sialic
Lateral Acid Sialidase acid Sclerosis Amyotrophic Sialic Alpha 2,6
Sialic Lateral Acid Sialidase acid Sclerosis Amyotrophic GalNAc
Hexos- GalNAc Lateral aminidase Sclerosis Amyotrophic GalNAc
Sialidase Hexos- GalNAc Lateral aminidase Sclerosis Amyotrophic
Sialic Hexos- Sialidase Sialic Lateral acid aminidase acid
Sclerosis Amyotrophic Galactose galactosidase Galactose Lateral
Sclerosis Amyotrophic Galactose sialidase galactosidase Galactose
Lateral Sclerosis Amyotrophic Fucose fucosidase Fucose Lateral
Sclerosis Amyotrophic Galactose Galactosidase Galactose Lateral
Sclerosis Amyotrophic GlcNAc hexos- GlcNAc Lateral aminidase
Sclerosis Amyotrophic Sulfate Sulfatase Sulfate Lateral Sclerosis
Amyotrophic Sulfated Sulfatase hexos- GlcNAc Lateral hexose
aminidase or Sclerosis GalNAc Amyotrophic Sulfated Sulfatase
Iduronidase IdoA or Lateral uronic or GlcA Sclerosis acid
glucuronidase Cerebral Palsy Sialic Sialidase Sialic Acid acid
Cerebral Palsy Sialic Alpha 2,8 Sialic Acid Sialidase acid Cerebral
Palsy Sialic Alpha 2,3 Sialic Acid Sialidase acid Cerebral Palsy
Sialic Alpha 2,6 Sialic Acid Sialidase acid Cerebral Palsy GalNAc
Hexos- GalNAc aminidase Cerebral Palsy GalNAc Sialidase Hexos-
GalNAc aminidase Cerebral Palsy Sialic Hexos- Sialidase Sialic Acid
aminidase acid Cerebral Palsy Galactose galactosidase Galactose
Cerebral Palsy Galactose sialidase galactosidase Galactose Cerebral
Palsy Fucose fucosidase Fucose Cerebral Palsy Galactose
Galactosidase Galactose Cerebral Palsy GlcNAc hexos- GlcNAc
aminidase Cerebral Palsy Sulfate Sulfatase Sulfate Cerebral Palsy
Sulfated Sulfatase hexos- GlcNAc hexose aminidase or GalNAc
Cerebral Palsy Sulfated Sulfatase Iduronidase IdoA or uronic or
GlcA acid glucuronidase Schizophrenia Sialic Sialidase Sialic Acid
acid Schizophrenia Sialic Alpha 2,8 Sialic Acid Sialidase acid
Schizophrenia Sialic Alpha 2,3 Sialic Acid Sialidase acid
Schizophrenia Sialic Alpha 2,6 Sialic Acid Sialidase acid
Schizophrenia GalNAc Hexos- GalNAc aminidase Schizophrenia GalNAc
Sialidase Hexos- GalNAc aminidase Schizophrenia Sialic Hexos-
Sialidase Sialic acid aminidase acid Schizophrenia Galactose
galactosidase Galactose Schizophrenia Galactose sialidase
galactosidase Galactose Schizophrenia Fucose fucosidase Fucose
Schizophrenia Galactose Galactosidase Galactose Schizophrenia
GlcNAc hexos- GlcNAc aminidase Schizophrenia Sulfate Sulfatase
Sulfate Schizophrenia Sulfated Sulfatase hexos- GlcNAc hexose
aminidase or GalNAc Schizophrenia Sulfated Sulfatase Iduronidase
IdoA or uronic or GlcA acid glucouronidase Bipolar Sialic Sialidase
Sialic Disorder Acid acid Bipolar Sialic Alpha 2,8 Sialic Disorder
Acid Sialidase acid Bipolar Sialic Alpha 2,3 Sialic Disorder Acid
Sialidase acid Bipolar Sialic Alpha 2,6 Sialic Disorder Acid
Sialidase acid Bipolar GalNAc Hexos- GalNAc Disorder aminidase
Bipolar GalNAc Sialidase Hexos- GalNAc Disorder aminidase Bipolar
Sialic Hexos- Sialidase Sialic Disorder acid aminidase acid Bipolar
Galactose galactosidase Galactose Disorder Bipolar Galactose
sialidase galactosidase Galactose Disorder Bipolar Fucose
fucosidase Fucose Disorder Bipolar Galactose Galactosidase
Galactose Disorder Bipolar GlcNAc hexos- GlcNAc Disorder aminidase
Bipolar Sulfate Sulfatase Sulfate Disorder Bipolar Sulfated
Sulfatase hexos- GlcNAc Disorder hexose aminidase or GalNAc Bipolar
Sulfated Sulfatase Iduronidase IdoA or Disorder uronic or GlcA acid
glucuronidase Depression Sialic Sialidase Sialic Acid acid
Depression Sialic Alpha 2,8 Sialic Acid Sialidase acid Depression
Sialic Alpha 2,3 Sialic Acid Sialidase acid Depression Sialic Alpha
2,6 Sialic Acid Sialidase acid Depression GalNAc Hexos- GalNAc
aminidase Depression GalNAc Sialidase Hexos- GalNAc aminidase
Depression Sialic Hexos- Sialidase Sialic acid aminidase acid
Depression Galactose galactosidase Galactose Depression Galactose
sialidase galactosidase Galactose Depression Fucose fucosidase
Fucose Depression Galactose Galactosidase Galactose Depression
GlcNAc hexos- GlcNAc aminidase Depression Sulfate Sulfatase Sulfate
Depression Sulfated Sulfatase hexos- GlcNAc hexose aminidase or
GalNAc Depression Sulfated Sulfatase Iduronidase IdoA or uronic or
GlcA acid glucuronidase Epilepsy Sialic Sialidase Sialic Acid acid
Epilepsy Sialic Alpha 2,8 Sialic Acid Sialidase acid Epilepsy
Sialic Alpha 2,3 Sialic Acid Sialidase acid Epilepsy Sialic Alpha
2,6 Sialic Acid Sialidase acid Epilepsy GalNAc Hexos- GalNAc
aminidase Epilepsy GalNAc Sialidase Hexos- GalNAc aminidase
Epilepsy Sialic Hexos- Sialidase Sialic acid aminidase acid
Epilepsy Galactose galactosidase Galactose Epilepsy Galactose
sialidase galactosidase Galactose Epilepsy Fucose fucosidase Fucose
Epilepsy Galactose Galactosidase Galactose Epilepsy GlcNAc hexos-
GlcNAc aminidase Epilepsy Sulfate Sulfatase Sulfate Epilepsy
Sulfated Sulfatase hexos- GlcNAc hexose aminidase or GalNAc
Epilepsy Sulfated Sulfatase Iduronidase IdoA or uronic or GlcA acid
glucuronidase Migraine Sialic Sialidase Sialic Acid acid Migraine
Sialic Alpha 2,8 Sialic Acid Sialidase acid Migraine Sialic Alpha
2,3 Sialic Acid Sialidase acid Migraine Sialic Alpha 2,6 Sialic
Acid Sialidase acid Migraine GalNAc Hexos- GalNAc aminidase
Migraine GalNAc Sialidase Hexos- GalNAc aminidase Migraine Sialic
Hexos- Sialidase Sialic acid aminidase acid Migraine Galactose
galactosidase Galactose Migraine Galactose sialidase galactosidase
Galactose Migraine Fucose fucosidase Fucose Migraine Galactose
Galactosidase Galactose Migraine GlcNAc hexos- GlcNAc aminidase
Migraine Sulfate Sulfatase Sulfate Migraine Sulfated Sulfatase
hexos- GlcNAc hexose aminidase or GalNcA Migraine Sulfated
Sulfatase Iduronidase IdoA or uronic or GlcA acid glucuronidase
Multiple Sialic Sialidase Sialic Sclerosis Acid acid Multiple
Sialic Alpha 2,8 Sialic Sclerosis Acid Sialidase acid
Multiple Sialic Alpha 2,3 Sialic Sclerosis Acid Sialidase acid
Multiple Sialic Alpha 2,6 Sialic Sclerosis Acid Sialidase acid
Multiple GalNAc Hexos- GalNAc Sclerosis aminidase Multiple GalNAc
Sialidase Hexos- GalNAc Sclerosis aminidase Multiple Sialic Hexos-
Sialidase Sialic Sclerosis acid aminidase acid Multiple Galactose
galactosidase Galactose Sclerosis Multiple Galactose sialidase
galactosidase Galactose Sclerosis Multiple Fucose fucosidase Fucose
Sclerosis Multiple Galactose Galactosidase Galactose Sclerosis
Multiple GlcNAc hexos- GlcNAc Sclerosis aminidase Multiple Sulfate
Sulfatase Sulfate Sclerosis Multiple Sulfated Sulfatase hexos-
GlcNAc Sclerosis hexose aminidase or GalNAc Multiple Sulfated
Sulfatase Iduronidase IdoA or Sclerosis uronic or GlcA acid
glucuronidase Parkinson`s Sialic Sialidase Sialic Acid acid
Parkinson`s Sialic Alpha 2,8 Sialic Acid Sialidase acid Parkinson`s
Sialic Alpha 2,3 Sialic Acid Sialidase acid Parkinson`s Sialic
Alpha 2,6 Sialic Acid Sialidase acid Parkinson's GalNAc Hexos-
GalNAc aminidase Parkinson`s GalNAc Sialidase Hexos- GalNAc
aminidase Parkinson`s Sialic Hexos- Sialidase Sialic acid aminidase
acid Parkinson`s Galactose galactosidase Galactose Parkinson`s
Galactose sialidase galactosidase Galactose Parkinson`s Fucose
fucosidase Fucose Parkinson`s Galactose Galactosidase Galactose
Parkinson`s GlcNAc hexos- GlcNAc aminidase Parkinson`s Sulfate
Sulfatase Sulfate Parkinson`s Sulfated Sulfatase hexos- GlcNAc
hexose aminidase or GalNAc Parkinson`s Sulfated Sulfatase
Iduronidase IdoA or uronic or GlcA acid glucuronidase Rheumatoid
Sialic Sialidase Sialic Arthritis Acid acid Rheumatoid Sialic Alpha
2,8 Sialic Arthritis Acid Sialidase acid Rheumatoid Sialic Alpha
2,3 Sialic Arthritis Acid Sialidase acid Rheumatoid Sialic Alpha
2,6 Sialic Arthritis Acid Sialidase acid Rheumatoid GalNAc Hexos-
GalNAc Arthritis aminidase Rheumatoid GalNAc Sialidase Hexos-
GalNAc Arthritis aminidase Rheumatoid Sialic Hexos- Sialidase
Sialic Arthritis acid aminidase acid Rheumatoid Galactose
galactosidase Galactose Arthritis Rheumatoid Galactose sialidase
galactosidase Galactose Arthritis Rheumatoid Fucose fucosidase
Fucose Arthritis Rheumatoid Galactose Galactosidase Galactose
Arthritis Rheumatoid GlcNAc hexos- GlcNAc Arthritis aminidase
Rheumatoid Sulfate Sulfatase Sulfate Arthritis Rheumatoid Sulfated
Sulfatase hexos- GlcNAc Arthritis hexose aminidase or GalNAc
Rheumatoid Sulfated Sulfatase Iduronidase IdoA or Arthritis uronic
or GlcA acid glucuronidase Psoriatic Sialic Sialidase Sialic
Arthritis Acid acid Psoriatic Sialic Alpha 2,8 Sialic Arthritis
Acid Sialidase acid Psoriatic Sialic Alpha 2,3 Sialic Arthritis
Acid Sialidase acid Psoriatic Sialic Alpha 2,6 Sialic Arthritis
Acid Sialidase acid Psoriatic GalNAc Hexos- GalNAc Arthritis
aminidase Psoriatic GalNAc Sialidase Hexos- GalNAc Arthritis
aminidase Psoriatic Sialic Hexos- Sialidase Sialic Arthritis acid
aminidase acid Psoriatic Galactose galactosidase Galactose
Arthritis Psoriatic Galactose sialidase galactosidase Galactose
Arthritis Psoriatic Fucose fucosidase Fucose Arthritis Psoriatic
Galactose Galactosidase Galactose Arthritis Psoriatic GlcNAc hexos-
GlcNAc Arthritis aminidase Psoriatic Sulfate Sulfatase Sulfate
Arthritis Psoriatic Sulfated Sulfatase hexos- GlcNAc Arthritis
hexose aminidase or GalNAc Psoriatic Sulfated Sulfatase Iduronidase
IdoA or Arthritis uronic or GlcA acid glucuronidase Asthma Sialic
Sialidase Sialic Acid acid Asthma Sialic Alpha 2,8 Sialic Acid
Sialidase acid Asthma Sialic Alpha 2,3 Sialic Acid Sialidase acid
Asthma Sialic Alpha 2,6 Sialic Acid Sialidase acid Asthma GalNAc
Hexos- GalNAc aminidase Asthma GalNAc Sialidase Hexos- GalNAc
aminidase Asthma Sialic Hexos- Sialidase Sialic acid aminidase acid
Asthma Galactose galactosidase Galactose Asthma Galactose sialidase
galactosidase Galactose Asthma Fucose fucosidase Fucose Asthma
Galactose Galactosidase Galactose Asthma GlcNAc hexos- GlcNAc
aminidase Asthma Sulfate Sulfatase Sulfate Asthma Sulfated
Sulfatase hexos- GlcNAc hexose aminidase or GalNAc Asthma Sulfated
Sulfatase Iduronidase IdoA or uronic or GlcA acid glucuronidase
Chronic Sialic Sialidase Sialic Obstructive Acid acid Pulmonary
Disorder Chronic Sialic Alpha 2,8 Sialic Obstructive Acid Sialidase
acid Pulmonary Disorder Chronic Sialic Alpha 2,3 Sialic Obstructive
Acid Sialidase acid Pulmonary Disorder Chronic Sialic Alpha 2,6
Sialic Obstructive Acid Sialidase acid Pulmonary Disorder Chronic
GalNAc Hexos- GalNAc Obstructive aminidase Pulmonary Disorder
Chronic GalNAc Sialidase Hexos- GalNAc Obstructive aminidase
Pulmonary Disorder Chronic Sialic Hexos- Sialidase Sialic
Obstructive acid aminidase acid Pulmonary Disorder Chronic
Galactose galactosidase Galactose Obstructive Pulmonary Disorder
Chronic Galactose sialidase galactosidase Galactose Obstructive
Pulmonary Disorder Chronic Fucose fucosidase Fucose Obstructive
Pulmonary Disorder Chronic Galactose Galactosidase Galactose
Obstructive Pulmonary Disorder Chronic GlcNAc hexos- GlcNAc
Obstructive aminidase Pulmonary Disorder Chronic Sulfate Sulfatase
Sulfate Obstructive Pulmonary Disorder Chronic Sulfated Sulfatase
hexos- GlcNAc Obstructive hexose aminidase or Pulmonary GalNAc
Disorder Chronic Sulfated Sulfatase Iduronidase IdoA or Obstructive
uronic or GlcA Pulmonary acid glucuronidase Disorder Lupus Sialic
Sialidase Sialic Acid acid Lupus Sialic Alpha 2,8 Sialic Acid
Sialidase acid Lupus Sialic Alpha 2,3 Sialic Acid Sialidase acid
Lupus Sialic Alpha 2,6 Sialic Acid Sialidase acid Lupus GalNAc
Hexos- GalNAc aminidase Lupus GalNAc Sialidase Hexos- GalNAc
aminidase Lupus Sialic Hexos- Sialidase Sialic acid aminidase acid
Lupus Galactose galactosidase Galactose Lupus Galactose sialidase
galactosidase Galactose Lupus Fucose fucosidase Fucose Lupus
Galactose Galactosidase Galactose Lupus GlcNAc hexos- GlcNAc
aminidase Lupus Sulfate Sulfatase Sulfate Lupus Sulfated Sulfatase
hexos- GlcNAc hexose aminidase or GalNAc Lupus Sulfated Sulfatase
Iduronidase IdoA or uronic or GlcA acid glucuronidase Hepatitis
Sialic Sialidase Sialic Acid acid Hepatitis Sialic Alpha 2,8 Sialic
Acid Sialidase acid Hepatitis Sialic Alpha 2,3 Sialic Acid
Sialidase acid Hepatitis Sialic Alpha 2,6 Sialic Acid Sialidase
acid Hepatitis GalNAc Hexos- GalNAc aminidase Hepatitis GalNAc
Sialidase Hexos- GalNAc aminidase Hepatitis Sialic Hexos- Sialidase
Sialic acid aminidase acid Hepatitis Galactose galactosidase
Galactose Hepatitis Galactose sialidase galactosidase Galactose
Hepatitis Fucose fucosidase Fucose Hepatitis Galactose
Galactosidase Galactose
Hepatitis GlcNAc hexos- GlcNAc aminidase Hepatitis Sulfate
Sulfatase Sulfate Hepatitis Sulfated Sulfatase hexos- GlcNAc hexose
aminidase or GalNAc Hepatitis Sulfated Sulfatase Iduronidase IdoA
or uronic or GlcA acid glucuronidase Renal Disease Sialic Sialidase
Sialic Acid acid Renal Disease Sialic Alpha 2,8 Sialic Acid
Sialidase acid Renal Disease Sialic Alpha 2,3 Sialic Acid Sialidase
acid Renal Disease Sialic Alpha 2,6 Sialic Acid Sialidase acid
Renal Disease GalNAc Hexos- GalNAc aminidase Renal Disease GalNAc
Sialidase Hexos- GalNAc aminidase Renal Disease Sialic Hexos-
Sialidase Sialic acid aminidase acid Renal Disease Galactose
galactosidase Galactose Renal Disease Galactose sialidase
galactosidase Galactose Renal Disease Fucose fucosidase Fucose
Renal Disease Galactose Galactosidase Galactose Renal Disease
GlcNAc hexos- GlcNAc aminidase Renal Disease Sulfate Sulfatase
Sulfate Renal Disease Sulfated Sulfatase hexos- GlcNAc hexose
aminidase or GalNAc Renal Disease Sulfated Sulfatase Iduronidase
IdoA or uronic or GlcA acid glucouronidase Sickle Cell Sialic
Sialidase Sialic Disease Acid acid Sickle Cell Sialic Alpha 2,8
Sialic Disease Acid Sialidase acid Sickle Cell Sialic Alpha 2,3
Sialic Disease Acid Sialidase acid Sickle Cell Sialic Alpha 2,6
Sialic Disease Acid Sialidase acid Sickle Cell GalNAc Hexos- GalNAc
Disease aminidase Sickle Cell GalNAc Sialidase Hexos- GalNAc
Disease aminidase Sickle Cell Sialic Hexos- Sialidase Sialic
Disease acid aminidase acid Sickle Cell Galactose galactosidase
Galactose Disease Sickle Cell Galactose sialidase galactosidase
Galactose Disease Sickle Cell Fucose fucosidase Fucose Disease
Sickle Cell Galactose Galactosidase Galactose Disease Sickle Cell
GlcNAc hexos- GlcNAc Disease aminidase Sickle Cell Sulfate
Sulfatase Sulfate Disease Sickle Cell Sulfated Sulfatase hexos-
GlcNAc Disease hexose aminidase or GalNAc Sickle Cell Sulfated
Sulfatase Iduronidase IdoA or Disease uronic or GlcA acid
glucuronidase Fibromyalgia Sialic Sialidase Sialic Acid acid
Fibromyalgia Sialic Alpha 2,8 Sialic Acid Sialidase acid
Fibromyalgia Sialic Alpha 2,3 Sialic Acid Sialidase acid
Fibromyalgia Sialic Alpha 2,6 Sialic Acid Sialidase acid
Fibromyalgia GalNAc Hexos- GalNAc aminidase Fibromyalgia GalNAc
Sialidase Hexos- GalNAc aminidase Fibromyalgia Sialic Hexos-
Sialidase Sialic acid aminidase acid Fibromyalgia Galactose
galactosidase Galactose Fibromyalgia Galactose sialidase
galactosidase Galactose Fibromyalgia Fucose fucosidase Fucose
Fibromyalgia Galactose Galactosidase Galactose Fibromyalgia GlcNAc
hexos- GlcNAc aminidase Fibromyalgia Sulfate Sulfatase Sulfate
Fibromyalgia Sulfated Sulfatase hexos- GlcNAc hexose aminidase or
GalNAc Fibromyalgia Sulfated Sulfatase Iduronidase IdoA or uronic
or GlcA acid glucouronidase Irritable Bowel Sialic Sialidase Sialic
Syndrome Acid acid Irritable Bowel Sialic Alpha 2,8 Sialic Syndrome
Acid Sialidase acid Irritable Bowel Sialic Alpha 2,3 Sialic
Syndrome Acid Sialidase acid Irritable Bowel Sialic Alpha 2,6
Sialic Syndrome Acid Sialidase acid Irritable Bowel GalNAc Hexos-
GalNAc Syndrome aminidase Irritable Bowel GalNAc Sialidase Hexos-
GalNAc Syndrome aminidase Irritable Bowel Sialic Hexos- Sialidase
Sialic Syndrome acid aminidase acid Irritable Bowel Galactose
galactosidase Galactose Syndrome Irritable Bowel Galactose
sialidase galactosidase Galactose Syndrome Irritable Bowel Fucose
fucosidase Fucose Syndrome Irritable Bowel Galactose Galactosidase
Galactose Syndrome Irritable Bowel GlcNAc hexos- GlcNAc Syndrome
aminidase Irritable Bowel Sulfate Sulfatase Sulfate Syndrome
Irritable Bowel Sulfated Sulfatase hexos- GlcNAc Syndrome hexose
aminidase or GalNAc Irritable Bowel Sulfated Sulfatase Iduronidase
IdoA or Syndrome uronic or GlcA acid glucouronidase Ulcer Sialic
Sialidase Sialic Acid acid Ulcer Sialic Alpha 2,8 Sialic Acid
Sialidase acid Ulcer Sialic Alpha 2,3 Sialic Acid Sialidase acid
Ulcer Sialic Alpha 2,6 Sialic Acid Sialidase acid Ulcer GalNAc
Hexos- GalNAc aminidase Ulcer GalNAc Sialidase Hexos- GalNAc Ulcer
aminidase Sialic Hexos- Sialidase Sialic Ulcer acid aminidase acid
Ulcer Galactose sialidase galactosidase Galactose Ulcer Fucose
fucosidase Fucose Ulcer Galactose Galactosidase Galactose Ulcer
GlcNAc hexos- GlcNAc aminidase Ulcer Sulfate Sulfatase Sulfate
Ulcer Sulfated Sulfatase hexos- GlcNAc hexose aminidase or GalNAc
Ulcer Sulfated Sulfatase Iduronidase IdoA or uronic or GlcA acid
glucouronidase Irritable Bowel Sialic Sialidase Sialic Disease Acid
acid Irritable Bowel Sialic Alpha 2,8 Sialic Disease Acid Sialidase
acid Irritable Bowel Sialic Alpha 2,3 Sialic Disease Acid Sialidase
acid Irritable Bowel Sialic Alpha 2,6 Sialic Disease Acid Sialidase
acid Irritable Bowel GalNAc Hexos- GalNAc Disease aminidase
Irritable Bowel GalNAc Sialidase Hexos- GalNAc Disease aminidase
Irritable Bowel Sialic Hexos- Sialidase Sialic Disease acid
aminidase acid Irritable Bowel Galactose galactosidase Galactose
Disease Irritable Bowel Galactose sialidase galactosidase Galactose
Disease Irritable Bowel Fucose fucosidase Fucose Disease Irritable
Bowel Galactose Galactosidase Galactose Disease Irritable Bowel
GlcNAc hexos- GlcNAc Disease aminidase Irritable Bowel Sulfate
Sulfatase Sulfate Disease Irritable Bowel Sulfated Sulfatase hexos-
GlcNAc Disease hexose aminidase or GalNAc Irritable Bowel Sulfated
Sulfatase Iduronidase IdoA or Disease uronic or GlcA acid
glucouronidase Coronary Artery Sialic Sialidase Sialic Disease Acid
acid Coronary Artery Sialic Alpha 2,8 Sialic Disease Acid Sialidase
acid Coronary Artery Sialic Alpha 2,3 Sialic Disease Acid Sialidase
acid Coronary Artery Sialic Alpha 2,6 Sialic Disease Acid Sialidase
acid Coronary Artery GalNAc Hexos- GalNAc Disease aminidase
Coronary Artery GalNAc Sialidase Hexos- GalNAc Disease aminidase
Coronary Artery Sialic Hexos- Sialidase Sialic Disease acid
aminidase acid Coronary Artery Galactose galactosidase Galactose
Disease Coronary Artery Galactose sialidase galactosidase Galactose
Disease Coronary Artery Fucose fucosidase Fucose Disease Coronary
Artery Galactose Galactosidase Galactose Disease Coronary Artery
GlcNAc hexos- GlcNAc Disease aminidase Coronary Artery Sulfate
Sulfatase Sulfate Disease Coronary Artery Sulfated Sulfatase hexos-
GlcNAc Disease hexose aminidase or GalNAc Coronary Artery Sulfated
Sulfatase Iduronidase IdoA or Disease uronic or GlcA acid
glucouronidase Restenosis Sialic Sialidase Sialic Acid acid
Restenosis Sialic Alpha 2,8 Sialic Acid Sialidase acid Restenosis
Sialic Alpha 2,3 Sialic Acid Sialidase acid Restenosis Sialic Alpha
2,6 Sialic Acid Sialidase acid Restenosis GalNAc Hexos- GalNAc
aminidase Restenosis GalNAc Sialidase Hexos- GalNAc aminidase
Restenosis Sialic Hexos- Sialidase Sialic acid aminidase acid
Restenosis Galactose galactosidase Galactose Restenosis Galactose
sialidase galactosidase Galactose Restenosis Fucose fucosidase
Fucose Restenosis Galactose Galactosidase Galactose Restenosis
GlcNAc hexos- GlcNAc aminidase Restenosis Sulfate Sulfatase Sulfate
Restenosis Sulfated Sulfatase hexos- GlcNAc hexose aminidase or
GalNAc Restenosis Sulfated Sulfatase Iduronidase IdoA or uronic or
GlcA acid glucouronidase Stroke Sialic Sialidase Sialic Acid acid
Stroke Sialic Alpha 2,8 Sialic Acid Sialidase acid Stroke Sialic
Alpha 2,3 Sialic Acid Sialidase acid Stroke Sialic Alpha 2,6
Sialic
Acid Sialidase acid Stroke GalNAc Hexos- GalNAc aminidase Stroke
GalNAc Sialidase Hexos- GalNAc aminidase Stroke Sialic Hexos-
Sialidase Sialic acid aminidase acid Stroke Galactose galactosidase
Galactose Stroke Galactose sialidase galactosidase Galactose Stroke
Fucose fucosidase Fucose Stroke Galactose Galactosidase Galactose
Stroke GlcNAc hexos- GlcNAc aminidase Stroke Sulfate Sulfatase
Sulfate Stroke Sulfated Sulfatase hexos- GlcNAc hexose aminidase or
GalNAc Stroke Sulfated Sulfatase Iduronidase IdoA or uronic or GlcA
acid glucouronidase Diabetes Sialic Sialidase Sialic Acid acid
Diabetes Sialic Alpha 2,8 Sialic Acid Sialidase acid Diabetes
Sialic Alpha 2,3 Sialic Acid Sialidase acid Diabetes Sialic Alpha
2,6 Sialic Acid Sialidase acid Diabetes GalNAc Hexos- GalNAc
aminidase Diabetes GalNAc Sialidase Hexos- GalNAc aminidase
Diabetes Sialic Hexos- Sialidase Sialic acid aminidase acid
Diabetes Galactose galactosidase Galactose Diabetes Galactose
sialidase galactosidase Galactose Diabetes Fucose fucosidase Fucose
Diabetes Galactose Galactosidase Galactose Diabetes GlcNAc hexos-
GlcNAc aminidase Diabetes Sulfate Sulfatase Sulfate Diabetes
Sulfated Sulfatase hexos- GlcNAc hexose aminidase or GalNAc
Diabetes Sulfated Sulfatase Iduronidase IdoA or uronic or GlcA acid
glucouronidase Hyper- Sialic Sialidase Sialic heparanemia Acid acid
Hyper- Sialic Alpha 2,8 Sialic heparanemia Acid Sialidase acid
Hyper- Sialic Alpha 2,3 Sialic heparanemia Acid Sialidase acid
Hyper- Sialic Alpha 2,6 Sialic heparanemia Acid Sialidase acid
Hyper- GalNAc Hexos- GalNAc heparanemia aminidase Hyper- GalNAc
Sialidase Hexos- GalNAc heparanemia aminidase Hyper- Sialic Hexos-
Sialidase Sialic heparanemia acid aminidase acid Hyper- Galactose
galactosidase Galactose heparanemia Hyper- Galactose sialidase
galactosidase Galactose heparanemia Hyper- Fucose fucosidase Fucose
heparanemia Hyper- Galactose Galactosidase Galactose heparanemia
Hyper- GlcNAc hexos- GlcNAc heparanemia aminidase Hyper- Sulfate
Sulfatase Sulfate heparanemia Hyper- Sulfated Sulfatase hexos-
GlcNAc heparanemia hexose aminidase or GalNAc Hyper- Sulfated
Sulfatase Iduronidase IdoA or heparanemia uronic or GlcA acid
glucouronidase Hyper- Sialic Sialidase Sialic gangliosidemia Acid
acid Hyper- Sialic Alpha 2,8 Sialic gangliosidemia Acid Sialidase
acid Hyper- Sialic Alpha 2,3 Sialic gangliosidemia Acid Sialidase
acid Hyper- Sialic Alpha 2,6 Sialic gangliosidemia Acid Sialidase
acid Hyper- GalNAc Hexos- GalNAc gangliosidemia aminidase Hyper-
GalNAc Sialidase Hexos- GalNAc gangliosidemia aminidase Hyper-
Sialic Hexos- Sialidase Sialic gangliosidemia acid aminidase acid
Hyper- Galactose sialidase galactosidase Galactose gangliosidemia
Hyper- Fucose fucosidase Fucose gangliosidemia Hyper- Galactose
Galactosidase Galactose gangliosidemia Hyper- GlcNAc hexos- GlcNAc
gangliosidemia aminidase Hyper- Sulfate Sulfatase Sulfate
gangliosidemia Hyper- Sulfated Sulfatase hexos- GlcNAc
gangliosidemia hexose aminidase or GalNAc Hyper- Sulfated Sulfatase
Iduronidase or IdoA or gangliosidemia uronic glucouronidase GlcA
acid Hyper- Sialic Sialidase Sialic mucinemia Acid acid Hyper-
Sialic Alpha 2,8 Sialic mucinemia Acid Sialidase acid Hyper- Sialic
Alpha 2,3 Sialic mucinemia Acid Sialidase acid Hyper- Sialic Alpha
2,6 Sialic mucinemia Acid Sialidase acid Hyper- GalNAc Hexos-
GalNAc mucinemia aminidase Hyper- GalNAc Sialidase Hexos- GalNAc
mucinemia aminidase Hyper- Sialic Hexos- Sialidase Sialic mucinemia
acid aminidase acid Hyper- Galactose galactosidase Galactose
mucinemia Hyper- Galactose sialidase galactosidase Galactose
mucinemia Hyper- Fucose fucosidase Fucose mucinemia Hyper-
Galactose Galactosidase Galactose mucinemia Hyper- GlcNAc hexos-
GlcNAc mucinemia aminidase Hyper- Sulfate Sulfatase Sulfate
mucinemia Hyper- Sulfated Sulfatase hexos- GlcNAc mucinemia hexose
aminidase or GalNAc Hyper- Sulfated Sulfatase Iduronidase IdoA or
mucinemia uronic or GlcA acid glucouronidase Hyper O-linked Sialic
Sialidase Sialic glycanemia Acid acid Hyper O-linked Sialic Alpha
2,8 Sialic glycanemia Acid Sialidase acid Hyper O-linked Sialic
Alpha 2,3 Sialic glycanemia Acid Sialidase acid Hyper O-linked
Sialic Alpha 2,6 Sialic glycanemia Acid Sialidase acid Hyper
O-linked GalNAc Hexos- GalNAc glycanemia aminidase Hyper O-linked
GalNAc Sialidase Hexos- GalNAc glycanemia aminidase Hyper O-linked
Sialic Hexos- Sialidase Sialic glycanemia acid aminidase acid Hyper
O-linked Galactose galactosidase Galactose glycanemia Hyper
O-linked Galactose sialidase galactosidase Galactose glycanemia
Hyper O-linked Fucose fucosidase Fucose glycanemia Hyper O-linked
Galactose Galactosidase Galactose glycanemia Hyper O-linked GlcNAc
hexos- GlcNAc glycanemia aminidase Hyper O-linked Sulfate Sulfatase
Sulfate glycanemia Hyper O-linked Sulfated Sulfatase hexos- GlcNAc
glycanemia hexose aminidase or GalNAc Hyper O-linked Sulfated
Sulfatase Iduronidase IdoA or glycanemia uronic or GlcA acid
glucouronidase Hyper N-linked Sialic Sialidase Sialic glycanemia
Acid acid Hyper N-linked Sialic Alpha 2,8 Sialic glycanemia Acid
Sialidase acid Hyper N-linked Sialic Alpha 2,3 Sialic glycanemia
Acid Sialidase acid Hyper N-linked Sialic Alpha 2,6 Sialic
glycanemia Acid Sialidase acid Hyper N-linked GalNAc Hexos- GalNAc
glycanemia aminidase Hyper N-linked GalNAc Sialidase Hexos- GalNAc
glycanemia aminidase Hyper N-linked Sialic Hexos- Sialidase Sialic
glycanemia acid aminidase acid Hyper N-linked Galactose
galactosidase Galactose glycanemia Hyper N-linked Galactose
sialidase galactosidase Galactose glycanemia Hyper N-linked Fucose
fucosidase Fucose glycanemia Hyper N-linked Galactose Galactosidase
Galactose glycanemia Hyper N-linked GlcNAc hexos- GlcNAc glycanemia
aminidase Hyper N-linked Sulfate Sulfatase Sulfate glycanemia Hyper
N-linked Sulfated Sulfatase hexos- GlcNAc glycanemia hexose
aminidase or GalNAc Hyper N-linked Sulfated Sulfatase Iduronidase
IdoA or glycanemia uronic or GlcA acid glucouronidase Hyper- Sialic
Sialidase Sialic sialylemia Acid acid Hyper- Sialic Alpha 2,8
Sialic sialylemia Acid Sialidase acid Hyper- Sialic Alpha 2,3
Sialic sialylemia Acid Sialidase acid Hyper- Sialic Alpha 2,6
Sialic sialylemia Acid Sialidase acid Hyper- GalNAc Hexos- GalNAc
sialylemia aminidase Hyper- GalNAc Sialidase Hexos- GalNAc
sialylemia aminidase Hyper- Sialic Hexos- Sialidase Sialic
sialylemia acid aminidase acid Hyper- Galactose galactosidase
Galactose sialylemia Hyper- Galactose sialidase galactosidase
Galactose sialylemia Hyper- Fucose fucosidase Fucose sialylemia
Hyper- Galactose Galactosidase Galactose sialylemia Hyper- GlcNAc
hexos- GlcNAc sialylemia aminidase Hyper- Sulfate Sulfatase Sulfate
sialylemia Hyper- Sulfated Sulfatase hexos- GlcNAc sialylemia
hexose aminidase or GalNAc Hyper- Sulfated Sulfatase Iduronidase
IdoA or sialylemia uronic or GlcA acid glucouronidase Hyper- Sialic
Sialidase Sialic fucosylemia Acid acid Hyper- Sialic Alpha 2,8
Sialic fucosylemia Acid Sialidase acid Hyper- Sialic Alpha 2,3
Sialic fucosylemia Acid Sialidase acid Hyper- Sialic Alpha 2,6
Sialic fucosylemia Acid Sialidase acid Hyper- GalNAc Hexos- GalNAc
fucosylemia aminidase Hyper- GalNAc Sialidase Hexos- GalNAc
fucosylemia aminidase Hyper- Sialic Hexos- Sialidase Sialic
fucosylemia acid aminidase acid
Hyper- Galactose galactosidase Galactose fucosylemia Hyper-
Galactose sialidase galactosidase Galactose fucosylemia Hyper-
Fucose fucosidase Fucose fucosylemia Hyper- Galactose Galactosidase
Galactose fucosylemia Hyper- GlcNAc hexos- GlcNAc fucosylemia
aminidase Hyper- Sulfate Sulfatase Sulfate fucosylemia Hyper-
Sulfated Sulfatase hexos- GlcNAc fucosylemia hexose aminidase or
GalNAc Hyper- Sulfated Sulfatase Iduronidase IdoA or fucosylemia
uronic or GlcA acid glucouronidase Hypersulfo- Sialic Sialidase
Sialic gycanemia Acid acid Hypersulfo- Sialic Alpha 2,8 Sialic
gycanemia Acid Sialidase acid Hypersulfo- Sialic Alpha 2,3 Sialic
gycanemia Acid Sialidase acid Hypersulfo- Sialic Alpha 2,6 Sialic
gycanemia Acid Sialidase acid Hypersulfo- GalNAc Hexos- GalNAc
gycanemia aminidase Hypersulfo- GalNAc Sialidase Hexos- GalNAc
gycanemia aminidase Hypersulfo- Sialic Hexos- Sialidase Sialic
gycanemia acid aminidase acid Hypersulfo- Galactose galactosidase
Galactose gycanemia Hypersulfo- Galactose sialidase galactosidase
Galactose gycanemia Hypersulfo- Fucose fucosidase Fucose gycanemia
Hypersulfo- Galactose Galactosidase Galactose gycanemia Hypersulfo-
GlcNAc hexos- GlcNAc gycanemia aminidase Hypersulfo- Sulfate
Sulfatase Sulfate gycanemia Hypersulfo- Sulfated Sulfatase hexos-
GlcNAc gycanemia hexose aminidase or GalNAc Hypersulfo- Sulfated
Sulfatase Iduronidase IdoA or gycanemia uronic or GlcA acid
glucouronidase
[0238] Provided herein are methods of diagnosing individuals
(including, e.g., a disease state or the severity of a disease
states) with an infectious disease state associated with abnormal
glycan accumulation. Provided in Table 15 are specific embodiments
of disease that are optionally diagnosed and/or monitored according
to various embodiments described herein. Table 15 also illustrates
various non-limiting embodiments of specific enzyme(s) that are
optionally utilized to treat a biological sample from an individual
suffering from or suspected of (e.g., through a pre- or preliminary
screening process) suffering from various infectious disease states
associated with abnormal glycan accumulation. Moreover, Table 15
further illustrates various glycan residual compounds that are
liberated in various embodiments described herein, such liberated
glycan residual compounds optionally being detected and/or measured
in order to diagnose and/or monitor various infectious disease
states.
TABLE-US-00015 TABLE 15 Infectious Diseases Primary Secondary
Glycan Non-Reducing Liberating Liberating Residual Disease end
structure Enzyme Enzyme Compound Bacterial Infections Mannose
Mannosidase Mannose Bacterial Infections Fucose Fucosidase Fucose
Bacterial Infections Glucose Glucosidase Glucose Bacterial
Infections Galactose Galactosidase Galactose Bacterial Infections
GlcNAc hexosaminidase GlcNAc Bacterial Infections GalNAc
hexosaminidase GalNAc Bacterial Infections Arabinose Arabinosidase
Arabinose Bacterial Infections Xylose Xylosidase Xylose Bacterial
Infections Ribose Ribosidase Ribose Bacterial Infections Lyxose
Lyxosidase Lyxose Bacterial Infections Talose Talosidase Talose
Bacterial Infections Idose Idosidase Idose Bacterial Infections
Gulose Gulosidase Gulose Bacterial Infections Altrose Altrosidase
Altrose Bacterial Infections Allose Allosidase Allose Fungal
Infections Mannose Mannosidase Mannose Fungal Infections Fucose
Fucosidase Fucose Fungal Infections Glucose Glucosidase Glucose
Fungal Infections Galactose Galactosidase Galactose Fungal
Infections GlcNAc hexosaminidase GlcNAc Fungal Infections GalNAc
hexosaminidase GalNAc Fungal Infections Arabinose Arabinosidase
Arabinose Fungal Infections Xylose Xylosidase Xylose Fungal
Infections Ribose Ribosidase Ribose Fungal Infections Lyxose
Lyxosidase Lyxose Fungal Infections Talose Talosidase Talose Fungal
Infections Idose Idosidase Idose Fungal Infections Gulose
Gulosidase Gulose Fungal Infections Altrose Altrosidase Altrose
Fungal Infections Allose Allosidase Allose Viral Infections Sialic
Acid Sialidase Sialic acid Viral Infections Sialic Acid Alpha 2,8
Sialic acid Sialidase Viral Infections Sialic Acid Alpha 2,3 Sialic
acid Sialidase Viral Infections Sialic Acid Alpha 2,6 Sialic acid
Sialidase Viral Infections GalNAc Hexosaminidase GalNAc Viral
Infections GalNAc Sialidase Hexosaminidase GalNAc Viral Infections
Sialic acid Hexosaminidase Sialidase Sialic acid Viral Infections
Galactose galactosidase Galactose Viral Infections Galactose
sialidase galactosidase Galactose Viral Infections Fucose
fucosidase Fucose Viral Infections Galactose Galactosidase
Galactose Viral Infections GlcNAc hexosaminidase GlcNAc Viral
Infections Sulfate Sulfatase Sulfate Viral Infections Sulfated
hexose Sulfatase hexosaminidase GlcNAc or GalNAc Viral Infections
Sulfated uronic acid Sulfatase Iduronidase or IdoA or GlcA
glucouronidase
[0239] FIG. 1 illustrates compounds present in a normal biological
sample not subject to an enzymatic glycan residual liberation
process described herein. FIG. 2 illustrates compounds present in a
normal biological subject to an enzymatic glycan residual
liberation process described herein. FIG. 3 illustrates compounds
present in a biological sample of an individual suffering from a
disorder associated with abnormal glycan accumulation not subject
to an enzymatic glycan residual liberation process described
herein. FIG. 4 illustrates compounds present in a biological sample
of an individual suffering from a disorder associated with abnormal
glycan accumulation subject to an enzymatic glycan residual
liberation process described herein.
Detecting and Measuring:
[0240] Glycan residual compounds (including, e.g.,
oligosaccharides, monosaccharides, sulfate, phosphate, sialic acid,
acetate, or the like) described herein are detected and/or measured
in processes described herein in any suitable manner. In some
embodiments, glycan residual compounds are detected and/or measured
in unmodified form. In other embodiments, glycan residual compounds
are tagged with a detectable label prior and the labeled glycan
residual compound is detected.
[0241] In some embodiments, non-labeled compounds are optionally
detected and/or measured in any suitable manner, e.g., by pH, by
quantitative nuclear magnetic resonance (NMR), or the like.
[0242] In various embodiments, a method described herein comprises
determining whether the amount of liberated glycan residue is
abnormal and such a determination comprises labeling the glycan
residue with a detectable label and measuring the amount of labeled
glycan residue with an analytical instrument. In specific
embodiments, the detectable label is a mass label, a radioisotope
label, a fluorescent label, a chromophore label, or affinity label.
In some embodiments, the amount of liberated glycan is measured
using UV-Vis spectroscopy, IR spectroscopy, mass spectrometry, or a
combination thereof.
[0243] In the various embodiments of any process or method
described herein, any suitable detectable label is optionally
utilized. In some embodiments, detectable labels useful in the
processes or methods described herein include, by way of
non-limiting example, mass labels, antibodies, affinity labels,
radioisotope labels, chromophores, fluorescent labels, or the
like.
[0244] Fluorescent labels suitable for use in various embodiments
herein include, by way of non-limiting example, 2-aminopyridine
(2-AP), 2-aminobenzoic acid (2-AA), 2-aminobenzamide (2-AB),
2-aminoacridone (AMAC), p-aminobenzoic acid ethyl ester (ABEE),
p-aminobenzonitrile (ABN), 2-amino-6-cyanoethylpyridine (ACP),
7-amino-4-methylcoumarine (AMC),
8-aminonaphthalene-1,3,6-trisulfate (ANTS),
7-aminonaphthalene-1,3-disulfide (ANDS), and
8-aminopyrene-1,3,6-trisulfate (APTS), or the like. The fluorescent
labels can be attached by reductive amination with the fluorescent
label and sodium cyanoborohydride or the like.
[0245] Mass labels suitable for use in various embodiments herein
include, by way of non-limiting example, D-2-anthranilic acid,
D-2-aminopyridine, D-methyl iodide, .sup.13C methyl iodide,
deuterated-pyridyl-amine, D-biotin or the like. The mass labels can
be attached by permethylation or reductive amination by any method
that is known to those of skill in the art.
[0246] Affinity labels suitable for use in various embodiments
herein include, by way of non-limiting example, biotin and
derivatives.
[0247] Radioisotope labels suitable for use in various embodiments
herein include, by way of non-limiting example, sodium borotritide
(NaB.sup.3H.sub.4), .sup.3H, .sup.14C, .sup.32P, .sup.35S, or the
like.
[0248] Chromophores suitable for use in various embodiments herein
include, by way of non-limiting example, 4-amino-1,1'-azobenzene,
4'-N,N-dimethylamino-4-aminoazobenzene, aminoazobenzene,
diaminoazobenzene, Direct Red 16, CI Acid Red 57, CI Acid Blue 45,
CI Acid Blue 22, CL Mordant Brown 13, CI Direct Orange 75, or the
like. The chromophores may be labeled by any method that is known
to those of skill in the art, such as reductive amination with the
chromophore and sodium cyanoborohydride.
[0249] In some embodiments, the detectable label is an antibody. In
specific embodiments, the antibody is attached to a detectable
compound, such as mass labels, radioisotope labels, chromophores,
fluorescent labels, or the like. In some embodiments, antibodies
are themselves detected and/or are detectable in various manners,
e.g., as a chromophore, a fluorophore, or the like; or with a probe
(e.g., using dot blot techniques, immune-detection techniques, or
the like).
[0250] In certain embodiments, detectable labels are detected
and/or quantified according to any process described herein using
any technique, particularly any technique suitable for the
detectable label utilized. In some embodiments, suitable detection
techniques include, by way of non-limiting example, one or more of
a mass spectrometer, a nuclear magnetic resonance spectrometer, a
UV-Vis spectrometer, an IR spectrometer, a fluorimeter, a
phosphorimeter, a radiation spectrometer (e.g., a scintillation
counter), a thin layer chromatographic technique, or the like. In
certain embodiments, in any process described herein, glycan
residual compounds are optionally directly detected using a
suitable technique, such as quantitative nuclear magnetic
resonance. Quantitative nuclear magnetic resonance is also
optionally utilized to quantify and/or detect the presence of a
detectable label. In certain embodiments, one or more glycan
residual compounds are optionally detected using a suitable liquid
chromatography mass spectrometer (LC-MS).
[0251] In some embodiments, glycan residual compounds are tagged
with an antibody or probe, and are quantified using any suitable
method (e.g., dot blot techniques, immune detection techniques
(e.g., ELISA), or the like).
[0252] Various analytical methods useful for the processes
described herein include, by way of non-limiting example, mass
spectrometry, chromatography, HPLC, UPLC, TLC, GC, HPAEC-PAD,
electrophoresis--capillary or gel, or the like. In certain
embodiments, wherein a chromatographic technique is utilized, any
suitable solvent system is optionally employed. In certain
embodiments, a column (e.g., Cosmogel DEAE, Tsk Gel DEAE, Cosmogel
QA, Cosmogel CM, Cosmogel SP, or the like) is optionally loaded
with an equilibrating solvent (e.g., a buffer or salt solution,
such as a potassium acetate solution, sodium chloride solution,
sodium acetate solution, ammonium acetate solution, or the like),
e.g., with a pH of about 6, 7, or 8. In some embodiments, the
buffer or salt solution has a concentration of about 10 mM, 20 mM,
30 mM, 50 mM, 100 mM, 500 mM, 1 M, 2 M, or the like. Any suitable
flow rate is used, e.g., 0.5 mL/min, 1 mL, min, 1.5 mL/min, 2
mL/min, or the like. Following equilibration, a linear gradient is
optionally utilized. In some embodiments, the linear gradient is
run over 1-20 min, 1-10 min, 10-20 min, 1-5 min, 5-10 min, or the
like. In certain embodiments, the gradient is a buffer or salt
solution, e.g., as described above (e.g., from 0 M to 0.5 M, from 0
M to 3 M, from 0.5 M to 2 M, from 0 M to 2 M, from 1M to 2M, from 0
M to 3 M, from 2 M to 0 M, from 3 M to 0 M, or the like). Once the
gradient has reached a final concentration, the eluent is
optionally held at the final concentration for a suitable period of
time (e.g., 1-20 min, 5-10 min, 10-15 min, 1-5 min, 1-10 min, 15-20
min, or the like). After the optional holding of the final
concentration, the eluent may be switched to a second solvent or
solvent system (e.g., an alcohol, such as methanol, ethanol, or
isopropanol, acetonitrile, water, or the like). The switch to the
second solvent system may be over a period of time, e.g., 15
seconds, 30 seconds, 45 seconds, 60 seconds, 2 min, 3 min, or the
like. The second solvent system is optionally held for a period of
time, such as 1 min, 2 min, 3 min, 4 min, 5 min, 6 min, or the
like. Following the second solvent system cycle, the column is
optionally restored to initial solvent conditions.
Purification:
[0253] In certain embodiments, methods described herein comprise
purifying a biological sample, e.g., to remove non-glycan compounds
from the biological sample. In some embodiments, a biological
sample is purified prior to transforming a glycan thereof.
[0254] In certain embodiments, a biological sample containing
glycans (purified or not) can also be prepared so that all free
glycan residual compounds (e.g., monosaccharides) that are
naturally present in the biological sample (i.e., as taken from an
individual and without being treated) are eliminated from the
sample to reduce background signal (for example using dialysis,
spin column, gel filtration, etc).
[0255] In some embodiments, any process described herein includes a
step of purifying a biological sample comprising removing
monosaccharides therefrom, removing sulfates therefrom, removing
phosphates therefrom, removing acetate therefrom, removing sialic
acid therefrom, or a combination thereof. For example, in some
embodiments, a biological sample is optionally placed in to a
defined MW cut off spin column (retains large molecules when spun),
optionally washed (e.g., with 1 or more volumes of water or
buffer), and/or the like.
[0256] In certain embodiments, purification of biological samples
may further or alternatively comprise, e.g., fractionation,
purification, enrichment, or the like of glycans contained therein.
In some instances, such purification techniques are suitable to
isolate and/or separate different glycan classes within the
biological sample prior to transformation of one or more of such
glycans. In more specific instances, such purification techniques
are used to isolate and/or separate different subsets of a single
glycan class (such as isolating complex N-linked glycans from
hybrid N-linked structures) prior to transformation of one or more
of such glycans. In certain embodiments, a biological sample is
optionally prepared in such a way to enrich for specific glycan
classes. For example, a PHA affinity column is optionally used to
isolate a sub-fraction of complex N-linked glycans while a Con A
column could be used to enrich in a different subset of N-linked
glycans.
[0257] In some embodiments, any process described herein comprises
purification of a glycan residual compound resulting from a process
described herein (e.g., purification of the glycan residual
compound prior to analysis thereof). For example, in some
embodiments, the glycan residual compound is optionally isolated by
any suitable process, such as by washing the free glycan residual
compound (e.g., through a defined MW cut off membrane or by any
other suitable method). Moreover, in certain embodiments, the
resulting isolated glycan residual compound containing composition
is optionally dried or otherwise treated to concentrate the sample
and subsequently analyzed for glycan residual compound content by
any suitable analytical technique.
[0258] In some embodiments, the processes described herein
comprises further treatment steps of the test and/or control
samples. For example, in some embodiments, the samples are
homogenized and/or purified. In specific embodiments homogenization
is achieved in any suitable manner including, by way of
non-limiting example, with a basic solution, sonication, tissue
grinding, or other chemical agents. In some embodiments, severity
of a disorder is determined if a certain threshold amount is
measured (e.g., as compared to a control or controls) or a
threshold signal (e.g., on a fluorimeter or other analytical device
utilized to detect and/or measure the generated biomarker).
Similarly, a carrier of a disorder described herein is, in certain
embodiments, determined if a certain threshold amount is measured
(e.g., as compared to a control or controls) or a threshold signal
(e.g., on a fluorimeter or other analytical device utilized to
detect and/or measure the generated biomarker).
[0259] In certain embodiments, samples, including test samples
and/or control samples, described herein are optionally purified
prior to glycan processing (e.g., lyase treatment) and/or
characterization. Test samples and/or control samples (i.e., one or
more or all of the glycans found therein) are optionally purified
using any suitable purification technique. Test samples and/or
control samples are optionally purified at any suitable point in a
process described herein, including before or after tagging of the
glycans founds within the sample. In certain embodiments,
purification techniques include centrifugation, electrophoresis,
chromatography (e.g., silica gel or alumina column chromatography),
gas chromatography, high performance liquid chromatography (HPLC)
(e.g., reverse phase HPLC on chiral or achiral columns), thin layer
chromatography, ion exchange chromatography, gel chromatography
(e.g., gel filtration or permeation or size exclusion
chromatography, gel electrophoresis), molecular sieve
chromatography, affinity chromatography, size exclusion, filtration
(e.g. through a florisil or activated charcoal plug),
precipitation, osmosis, recrystallization, fluorous phase
purification, distillation, extraction, chromatofocusing,
supercritical fluid extraction, preparative flash chromatography
(e.g., flash chromatography using a UV-Vis detector and/or a mass
spectrometer (e.g., using the Biotage.RTM. suite of products) or
the like.
[0260] In some embodiments, glycans, such as heparan sulfate, are
naturally found attached to a core protein (together forming a
proteoglycan) or a lipid. In some embodiments, provided herein are
purification processes of separating glycan fragments (e.g.,
heparan sulfate fragments) from proteoglycans or glycolipids prior
to processing the glycan for processing and analysis.
Monitoring Therapy
[0261] Provided in certain embodiments are methods of treating
disorders associated with the abnormal degradation, biosynthesis
and/or accumulation of glycans, the methods comprising: [0262] a.
administering an agent for treating disorders associated with the
abnormal degradation, biosynthesis and/or accumulation of glycans
(e.g., an anti-LSD agent, an anti-cancer agent, or the like) to an
individual in need thereof; [0263] b. monitoring the accumulation
of glycans in the individual using any process described herein for
detecting or quantifying the amount of glycan residual compounds
(e.g., mono-saccharides, sulfate, or the like) present in a lyase
digested biological sample (e.g., urine, serum, plasma, or CSF
sample) according to any process described herein.
[0264] Provided in further or alternative embodiments are methods
of monitoring the treatment of disorders associated with the
abnormal degradation, biosynthesis and/or accumulation of glycans,
the methods comprising the following steps: [0265] a. following
administration of an agent for treating a disorder associated with
the abnormal degradation, biosynthesis and/or accumulation of
glycans (e.g., an anti-LSD agent, an anti-cancer agent, or the
like) to an individual in need thereof, generating a biomarker
comprising of one or more non-reducing end glycan residual compound
(e.g., monosaccharide).
[0266] In some embodiments, the biomarker is a saturated
monosaccharide and is generated by treating a population of
glycans, in or isolated from a biological sample from the
individual, with at least one digesting glycan enzymes, wherein
prior to enzyme treatment, the biomarker is not present in
abundance in samples from individuals with the disease or condition
relative to individuals without the disease or condition. In
certain embodiments, monitoring of the accumulation of glycans
comprises using an analytical instrument to detect the presence of
and/or measure the amount of the biomarker produced and displaying
or recording the presence of or a measure of a population of the
biomarker; wherein the presence of and/or measure the amount of the
biomarker is utilized to monitor the treatment.
[0267] In some embodiments, the agent is administered one or more
times. In certain embodiments, the agent is administered multiple
times. In some embodiments, the agent is administered in a loading
dose one or more times (e.g., in a loading dosing schedule) and
subsequently administered in a maintenance dose (e.g., in a
maintenance dosing schedule, such as three times a day, twice a
day, once a day, once every two days, once every three days, once
every four days, once a week, or the like). In some embodiments,
when glycan (as measure by one or more glycan residual compound(s))
accumulation begins to increase or accelerate, the dose is
optionally adjusted (e.g., the maintenance dose is increased, or an
additional loading dose or dosing schedule is utilized).
[0268] In some embodiments, monitoring the accumulation of glycans
comprises repeating the step of: using an analytical instrument to
detect the presence of and/or measure the amount of a population of
one or more glycan residual compounds present in a transformed
biological sample that has been prepared by treating a population
of glycans, in or isolated from a biological sample from the
individual, with at least one digesting glycan lyase to transform
the glycan into the population of the one or more glycan residual
compounds. In specific embodiments, the step is repeated at
periodic intervals (e.g., every day, every other day, every 2 days,
every 3 days, every 4 days, every week, every month, every 3
months, quarterly, every 6 months, yearly, or the like), at regular
times following a dose (e.g., 4 hours after a administration of the
agent, 6 hours after administration of the agent, 8 hours after
administration of the agent, 12 hours after administration of the
agent, or the like), prior to administration of the dose (e.g.,
immediately prior to administration of the agent, 2 hours prior to
administration of the agent, or the like), or any other monitoring
schedule.
[0269] In some embodiments, the monitoring of the accumulation of
glycan is conducted over a period of time, e.g., over a week, two
weeks, a month, two months, three months, six months, a year, or
the like. In some embodiments, the method for quantifying the
amount of one or more glycan residual compounds in a lyase digested
biological sample (e.g., urine, serum, plasma, or CSF) comprises
detecting and/or measuring (e.g., with an analytical device), one
or more glycan residual compounds within the lyase digested
biological sample from the individual after the biological sample
obtained from the individual has been treated with one or more
glycan lyases. In certain embodiments, such glycan lyases are
suitable for preparing glycan residual compounds from the glycan
present in the biological sample obtained from the individual. In
certain instances a representative portion of the one or more
glycan residual compounds in the transformed biological sample is
tagged with any suitable detectable label (e.g., a mass label, a
radioisotope label, a fluorescent label, a chromophore label,
affinity label, an antibody). In some embodiments, the process
comprises displaying or recording such a characterization of the
population of glycan residual compounds and/or tagged glycan
residual compounds.
[0270] In some embodiments, the agent described in a therapy herein
includes glycan accumulation inhibitors, agents that promote glycan
degradation, agents that activate enzymes that degrade glycans,
agents that inhibit biosynthesis of glycans, or the like. In some
embodiments, the agent that modulates glycan biosynthesis is an
agent that selectively modulates heparan sulfate biosynthesis, an
agent that selectively modulates chondroitin sulfate biosynthesis,
an agent that selectively modulates dermatan sulfate biosynthesis,
an agent that selectively modulates keratan sulfate biosynthesis,
an agent that selectively modulates hyaluronan biosynthesis, or a
combination thereof. Anti-LSD drugs include, by way of non-limiting
example, Imiglucerase (Cerazyme), laronidase (Aldurazyme),
idursulfase (Elaprase), galsulfase (Naglazyme), agalsidase beta
(Fabrazyme), alglucosidase alfa (Myozyme), agalsidase alfa
(Replagal), miglustat (Zavesca).
[0271] In some embodiments, one or more of the anti-cancer agents
are proapoptotic agents. Examples of anti-cancer agents include, by
way of non-limiting example: gossyphol, genasense, polyphenol E,
Chlorofusin, all trans-retinoic acid (ATRA), bryostatin, tumor
necrosis factor-related apoptosis-inducing ligand (TRAIL),
5-aza-2'-deoxycytidine, all trans retinoic acid, doxorubicin,
vincristine, etoposide, gemcitabine, imatinib (Gleevec.RTM.),
geldanamycin, 17-N-Allylamino-17-Demethoxygeldanamycin (17-AAG),
flavopiridol, LY294002, bortezomib, trastuzumab, BAY 11-7082,
PKC412, or PD184352, Taxol.TM., also referred to as "paclitaxel",
which is a well-known anti-cancer drug which acts by enhancing and
stabilizing microtubule formation, and analogs of Taxol.TM., such
as Taxotere.TM.. Compounds that have the basic taxane skeleton as a
common structure feature, have also been shown to have the ability
to arrest cells in the G2-M phases due to stabilized microtubules
and may be useful for treating cancer in combination with the
compounds described herein.
[0272] Further examples of anti-cancer agents include inhibitors of
mitogen-activated protein kinase signaling, e.g., U0126, PD98059,
PD184352, PD0325901, ARRY-142886, SB239063, SP600125, BAY 43-9006,
wortmannin, or LY294002; Syk inhibitors; mTOR inhibitors; and
antibodies (e.g., rituxan).
[0273] Other anti-cancer agents include Adriamycin, Dactinomycin,
Bleomycin, Vinblastine, Cisplatin, acivicin; aclarubicin; acodazole
hydrochloride; acronine; adozelesin; aldesleukin; altretamine;
ambomycin; ametantrone acetate; aminoglutethimide; amsacrine;
anastrozole; anthramycin; asparaginase; asperlin; azacitidine;
azetepa; azotomycin; batimastat; benzodepa; bicalutamide;
bisantrene hydrochloride; bisnafide dimesylate; bizelesin;
bleomycin sulfate; brequinar sodium; bropirimine; busulfan;
cactinomycin; calusterone; caracemide; carbetimer; carboplatin;
carmustine; carubicin hydrochloride; carzelesin; cedefingol;
chlorambucil; cirolemycin; cladribine; crisnatol mesylate;
cyclophosphamide; cytarabine; dacarbazine; daunorubicin
hydrochloride; decitabine; dexormaplatin; dezaguanine; dezaguanine
mesylate; diaziquone; doxorubicin; doxorubicin hydrochloride;
droloxifene; droloxifene citrate; dromostanolone propionate;
duazomycin; edatrexate; eflornithine hydrochloride; elsamitrucin;
enloplatin; enpromate; epipropidine; epirubicin hydrochloride;
erbulozole; esorubicin hydrochloride; estramustine; estramustine
phosphate sodium; etanidazole; etoposide; etoposide phosphate;
etoprine; fadrozole hydrochloride; fazarabine; fenretinide;
floxuridine; fludarabine phosphate; fluorouracil; flurocitabine;
fosquidone; fostriecin sodium; gemcitabine; gemcitabine
hydrochloride; hydroxyurea; idarubicin hydrochloride; ifosfamide;
iimofosine; interleukin Il (including recombinant interleukin II,
or rlL2), interferon alfa-2a; interferon alfa-2b; interferon
alfa-n1; interferon alfa-n3; interferon beta-1 a; interferon
gamma-1 b; iproplatin; irinotecan hydrochloride; lanreotide
acetate; letrozole; leuprolide acetate; liarozole hydrochloride;
lometrexol sodium; lomustine; losoxantrone hydrochloride;
masoprocol; maytansine; mechlorethamine hydrochloride; megestrol
acetate; melengestrol acetate; melphalan; menogaril;
mercaptopurine; methotrexate; methotrexate sodium; metoprine;
meturedepa; mitindomide; mitocarcin; mitocromin; mitogillin;
mitomalcin; mitomycin; mitosper; mitotane; mitoxantrone
hydrochloride; mycophenolic acid; nocodazoie; nogalamycin;
ormaplatin; oxisuran; pegaspargase; peliomycin; pentamustine;
peplomycin sulfate; perfosfamide; pipobroman; piposulfan;
piroxantrone hydrochloride; plicamycin; plomestane; porfimer
sodium; porfiromycin; prednimustine; procarbazine hydrochloride;
puromycin; puromycin hydrochloride; pyrazofurin; riboprine;
rogletimide; safingol; safingol hydrochloride; semustine;
simtrazene; sparfosate sodium; sparsomycin; spirogermanium
hydrochloride; spiromustine; spiroplatin; streptonigrin;
streptozocin; sulofenur; talisomycin; tecogalan sodium; tegafur;
teloxantrone hydrochloride; temoporfin; teniposide; teroxirone;
testolactone; thiamiprine; thioguanine; thiotepa; tiazofurin;
tirapazamine; toremifene citrate; trestolone acetate; triciribine
phosphate; trimetrexate; trimetrexate glucuronate; triptorelin;
tubulozole hydrochloride; uracil mustard; uredepa; vapreotide;
verteporfin; vinblastine sulfate; vincristine sulfate; vindesine;
vindesine sulfate; vinepidine sulfate; vinglycinate sulfate;
vinleurosine sulfate; vinorelbine tartrate; vinrosidine sulfate;
vinzolidine sulfate; vorozole; zeniplatin; zinostatin; zorubicin
hydrochloride.
[0274] Other anti-cancer agents include: 20-epi-1, 25
dihydroxyvitamin D3; 5-ethynyluracil; abiraterone; aclarubicin;
acylfulvene; adecypenol; adozelesin; aldesleukin; ALL-TK
antagonists; altretamine; ambamustine; amidox; amifostine;
aminolevulinic acid; amrubicin; amsacrine; anagrelide; anastrozole;
andrographolide; angiogenesis inhibitors; antagonist D; antagonist
G; antarelix; anti-dorsalizing morphogenetic protein-1;
antiandrogen, prostatic carcinoma; antiestrogen; antineoplaston;
antisense oligonucleotides; aphidicolin glycinate; apoptosis gene
modulators; apoptosis regulators; apurinic acid; ara-CDP-DL-PTBA;
arginine deaminase; asulacrine; atamestane; atrimustine;
axinastatin 1; axinastatin 2; axinastatin 3; azasetron; azatoxin;
azatyrosine; baccatin III derivatives; balanol; batimastat; BCR/ABL
antagonists; benzochlorins; benzoylstaurosporine; beta lactam
derivatives; beta-alethine; betaclamycin B; betulinic acid; bFGF
inhibitor; bicalutamide; bisantrene; bisaziridinylspermine;
bisnafide; bistratene A; bizelesin; breflate; bropirimine;
budotitane; buthionine sulfoximine; calcipotriol; calphostin C;
camptothecin derivatives; canarypox IL-2; capecitabine;
carboxamide-amino-triazole; carboxyamidotriazole; CaRest M3; CARN
700; cartilage derived inhibitor; carzelesin; casein kinase
inhibitors (ICOS); castanospermine; cecropin B; cetrorelix;
chlorins; chloroquinoxaline sulfonamide; cicaprost; cis-porphyrin;
cladribine; clomifene analogues; clotrimazole; collismycin A;
collismycin B; combretastatin A4; combretastatin analogue;
conagenin; crambescidin 816; crisnatol; cryptophycin 8;
cryptophycin A derivatives; curacin A; cyclopentanthraquinones;
cycloplatam; cypemycin; cytarabine ocfosfate; cytolytic factor;
cytostatin; dacliximab; decitabine; dehydrodidemnin B; deslorelin;
dexamethasone; dexifosfamide; dexrazoxane; dexverapamil;
diaziquone; didemnin B; didox; diethylnorspermine;
dihydro-5-azacytidine; 9-dioxamycin; diphenyl spiromustine;
docosanol; dolasetron; doxifluridine; droloxifene; dronabinol;
duocarmycin SA; ebselen; ecomustine; edelfosine; edrecolomab;
eflornithine; elemene; emitefur; epirubicin; epristeride;
estramustine analogue; estrogen agonists; estrogen antagonists;
etanidazole; etoposide phosphate; exemestane; fadrozole;
fazarabine; fenretinide; filgrastim; finasteride; flavopiridol;
flezelastine; fluasterone; fludarabine; fluorodaunorunicin
hydrochloride; forfenimex; formestane; fostriecin; fotemustine;
gadolinium texaphyrin; gallium nitrate; galocitabine; ganirelix;
gelatinase inhibitors; gemcitabine; glutathione inhibitors;
hepsulfam; heregulin; hexamethylene bisacetamide; hypericin;
ibandronic acid; idarubicin; idoxifene; idramantone; ilmofosine;
ilomastat; imidazoacridones; imiquimod; immunostimulant peptides;
insulin-like growth factor-1 receptor inhibitor; interferon
agonists; interferons; interleukins; iobenguane; iododoxorubicin;
ipomeanol, 4-; iroplact; irsogladine; isobengazole;
isohomohalicondrin B; itasetron; jasplakinolide; kahalalide F;
lamellarin-N triacetate; lanreotide; leinamycin; lenograstim;
lentinan sulfate; leptolstatin; letrozole; leukemia inhibiting
factor; leukocyte alpha interferon;
leuprolide+estrogen+progesterone; leuprorelin; levamisole;
liarozole; linear polyamine analogue; lipophilic disaccharide
peptide; lipophilic platinum compounds; lissoclinamide 7;
lobaplatin; lombricine; lometrexol; lonidamine; losoxantrone;
lovastatin; loxoribine; lurtotecan; lutetium texaphyrin;
lysofylline; lytic peptides; maitansine; mannostatin A; marimastat;
masoprocol; maspin; matrilysin inhibitors; matrix metalloproteinase
inhibitors; menogaril; merbarone; meterelin; methioninase;
metoclopramide; MIF inhibitor; mifepristone; miltefosine;
mirimostim; mismatched double stranded RNA; mitoguazone;
mitolactol; mitomycin analogues; mitonafide; mitotoxin fibroblast
growth factor-saporin; mitoxantrone; mofarotene; molgramostim;
monoclonal antibody, human chorionic gonadotrophin; monophosphoryl
lipid A+myobacterium cell wall sk; mopidamol; multiple drug
resistance gene inhibitor; multiple tumor suppressor 1-based
therapy; mustard anticancer agent; mycaperoxide B; mycobacterial
cell wall extract; myriaporone; N-acetyldinaline; N-substituted
benzamides; nafarelin; nagrestip; naloxone+pentazocine; napavin;
naphterpin; nartograstim; nedaplatin; nemorubicin; neridronic acid;
neutral endopeptidase; nilutamide; nisamycin; nitric oxide
modulators; nitroxide antioxidant; nitrullyn; O6-benzylguanine;
octreotide; okicenone; oligonucleotides; onapristone; ondansetron;
ondansetron; oracin; oral cytokine inducer; ormaplatin; osaterone;
oxaliplatin; oxaunomycin; palauamine; palmitoylrhizoxin; pamidronic
acid; panaxytriol; panomifene; parabactin; pazelliptine;
pegaspargase; peldesine; pentosan polysulfate sodium; pentostatin;
pentrozole; perflubron; perfosfamide; perillyl alcohol;
phenazinomycin; phenylacetate; phosphatase inhibitors; picibanil;
pilocarpine hydrochloride; pirarubicin; piritrexim; placetin A;
placetin B; plasminogen activator inhibitor; platinum complex;
platinum compounds; platinum-triamine complex; porfimer sodium;
porfiromycin; prednisone; propyl bis-acridone; prostaglandin J2;
proteasome inhibitors; protein A-based immune modulator; protein
kinase C inhibitor; protein kinase C inhibitors, microalgal;
protein tyrosine phosphatase inhibitors; purine nucleoside
phosphorylase inhibitors; purpurins; pyrazoloacridine;
pyridoxylated hemoglobin polyoxyethylerie conjugate; raf
antagonists; raltitrexed; ramosetron; ras farnesyl protein
transferase inhibitors; ras inhibitors; ras-GAP inhibitor;
retelliptine demethylated; rhenium Re 186 etidronate; rhizoxin;
ribozymes; RII retinamide; rogletimide; rohitukine; romurtide;
roquinimex; rubiginone B 1; ruboxyl; safingol; saintopin; SarCNU;
sarcophytol A; sargramostim; Sdi 1 mimetics; semustine; senescence
derived inhibitor 1; sense oligonucleotides; signal transduction
inhibitors; signal transduction modulators; single chain
antigen-binding protein; sizofiran; sobuzoxane; sodium borocaptate;
sodium phenylacetate; solverol; somatomedin binding protein;
sonermin; sparfosic acid; spicamycin D; spiromustine; splenopentin;
spongistatin 1; squalamine; stem cell inhibitor; stem-cell division
inhibitors; stipiamide; stromelysin inhibitors; sulfinosine;
superactive vasoactive intestinal peptide antagonist; suradista;
suramin; swainsonine; synthetic glycosaminoglycans; tallimustine;
tamoxifen methiodide; tauromustine; tazarotene; tecogalan sodium;
tegafur; tellurapyrylium; telomerase inhibitors; temoporfin;
temozolomide; teniposide; tetrachlorodecaoxide; tetrazomine;
thaliblastine; thiocoraline; thrombopoietin; thrombopoietin
mimetic; thymalfasin; thymopoietin receptor agonist; thymotrinan;
thyroid stimulating hormone; tin ethyl etiopurpurin; tirapazamine;
titanocene bichloride; topsentin; toremifene; totipotent stem cell
factor; translation inhibitors; tretinoin; triacetyluridine;
triciribine; trimetrexate; triptorelin; tropisetron; turosteride;
tyrosine kinase inhibitors; tyrphostins; UBC inhibitors; ubenimex;
urogenital sinus-derived growth inhibitory factor; urokinase
receptor antagonists; vapreotide; variolin B; vector system,
erythrocyte gene therapy; velaresol; veramine; verdins;
verteporfin; vinorelbine; vinxaltine; vitaxin; vorozole;
zanoterone; zeniplatin; zilascorb; and zinostatin stimalamer.
[0275] Yet other anticancer agents that include alkylating agents,
antimetabolites, natural products, or hormones, e.g., nitrogen
mustards (e.g., mechloroethamine, cyclophosphamide, chlorambucil,
etc.), alkyl sulfonates (e.g., busulfan), nitrosoureas (e.g.,
carmustine, lomusitne, etc.), or triazenes (decarbazine, etc.).
Examples of antimetabolites include but are not limited to folic
acid analog (e.g., methotrexate), or pyrimidine analogs (e.g.,
Cytarabine), purine analogs (e.g., mercaptopurine, thioguanine,
pentostatin).
[0276] Examples of natural products include but are not limited to
vinca alkaloids (e.g., vinblastin, vincristine),
epipodophyllotoxins (e.g., etoposide), antibiotics (e.g.,
daunorubicin, doxorubicin, bleomycin), enzymes (e.g.,
L-asparaginase), or biological response modifiers (e.g., interferon
alpha).
[0277] Examples of alkylating agents include, but are not limited
to, nitrogen mustards (e.g., mechloroethamine, cyclophosphamide,
chlorambucil, meiphalan, etc.), ethylenimine and methylmelamines
(e.g., hexamethlymelamine, thiotepa), alkyl sulfonates (e.g.,
busulfan), nitrosoureas (e.g., carmustine, lomusitne, semustine,
streptozocin, etc.), or triazenes (decarbazine, etc.). Examples of
antimetabolites include, but are not limited to folic acid analog
(e.g., methotrexate), or pyrimidine analogs (e.g., fluorouracil,
floxouridine, Cytarabine), purine analogs (e.g., mercaptopurine,
thioguanine, pentostatin.
[0278] Examples of hormones and antagonists include, but are not
limited to, adrenocorticosteroids (e.g., prednisone), progestins
(e.g., hydroxyprogesterone caproate, megestrol acetate,
medroxyprogesterone acetate), estrogens (e.g., diethlystilbestrol,
ethinyl estradiol), antiestrogen (e.g., tamoxifen), androgens
(e.g., testosterone propionate, fluoxymesterone), antiandrogen
(e.g., flutamide), gonadotropin releasing hormone analog (e.g.,
leuprolide). Other agents that can be used in the methods and
compositions described herein for the treatment or prevention of
cancer include platinum coordination complexes (e.g., cisplatin,
carboplatin), anthracenedione (e.g., mitoxantrone), substituted
urea (e.g., hydroxyurea), methyl hydrazine derivative (e.g.,
procarbazine), adrenocortical suppressant (e.g., mitotane,
aminoglutethimide).
[0279] In some instances, the detection and/or the quantification
of the identity and/or amount of glycan residual compounds present
in a biological sample is used to identify and/or diagnose a
disorder associated with abnormal degradation, biosynthesis and/or
accumulation of glycan in an individual suspected of having such a
disorder.
[0280] In some instances, the detection and/or the quantification
of the identity and/or amount of glycan residual compounds present
in the biological sample is used to monitor severity and course of
the disease in an individual diagnosed with or suspected of having
a disorder associated with the abnormal degradation, biosynthesis
and/or accumulation of glycans. In some instances, the detection
and/or the quantification of the identity and/or amount of glycan
residual compounds present in the biological sample is used to
calculate the administered dose of an agent that modulates (e.g.,
promotes and/or inhibits) glycan biosynthesis and/or
degradation.
[0281] In certain instances, wherein following administration of a
selected dose of a therapeutic agent utilized in a therapeutic
method described herein, an individual's condition does not
improve, the detection and/or the quantification of the identity
and/or amount of glycan residual compounds present in a biological
sample provides for a treatment regimen to be modified depending on
the severity and course of the disease, disorder or condition,
previous therapy, the individual's health status and response to
the drugs, and the judgment of the treating physician.
[0282] In certain embodiments, monitoring the accumulation of
glycans in the individual comprises detecting or quantifying the
amount of an glycan residual compounds (or one or more glycan
residual compounds) in a sample obtained from the individual (e.g.,
according to any method described herein) to obtain a first
accumulation result (e.g., an initial reading before treatment has
begun, or at any other time) and a second accumulation result that
is subsequent to obtaining the first result. In some embodiments,
the second result is compared to the first result to determine if
the treatment is effectively reducing, maintaining, or reducing the
rate of increasing the glycan residual compounds levels in a
substantially identically obtained sample from the individual being
treated. In certain embodiments, depending on the difference
between the first and second results, the treatment can be altered,
e.g., to increase or decrease the amount of agent administered; to
substitute the therapeutic agent with an alternative therapeutic
agent; or the like. In certain embodiments, the dose of the
therapeutic agent is decreased to a maintenance level (e.g., if the
glycan residual compound level has been reduced sufficiently);
further monitoring of glycan residual compound levels is optional
in such situation, e.g., to ensure that reduced or maintained
levels of glycan residual compounds (e.g., monosaccharide(s)) are
achieved.
[0283] Alternatively, provided herein is a method of detecting
response to therapy in an individual or a method of predicting
response to therapy in an individual comprising: [0284] a.
administering an agent for treating a disorder associated with the
abnormal degradation, biosynthesis and/or accumulation of glycans
to a plurality of cells from an individual in need thereof (e.g., a
plurality of fibroblasts, serum, plasma, or CSF cells from a human
suffering from a disorder associated with the abnormal degradation,
biosynthesis and/or accumulation of glycans, such as an LSD or
cancer); [0285] b. monitoring the accumulation of glycans in the
plurality of cells using any process described herein for detecting
or quantifying the amount of glycan residual compounds (e.g.,
monosaccharides, sulfate, sialic acid, phosphate, acetate, or the
like) present in a lyase digested biological sample from the
plurality of cells according to any process described herein.
[0286] In specific embodiments, the glycan residual compound(s)
detected or measured is one or more monosaccharide. It is to be
understood that a plurality of cells from an individual includes
cells that are directly taken from the individual, and/or cells
that are taken from an individual followed by culturing to expand
the population thereof.
EXAMPLES
Example 1
[0287] To illustrate the methods described herein, we have used
human urine sample from normal patients and patients diagnosed with
MPS IIIA. MPS IIIA patients have reduced function of the lysosomal
enzyme that de-N-sulfates the nonreducing end glucosamine residues
present in heparan sulfate. This unique nonreducing end glycan
residual (N-sulfated GlcN) can be liberated by treating the glycans
with heparin lyases and quantified by fluorescent detection on
HPLC. As shown below, glycans prepared in this manner from normal
individuals lack N-sulfate GlcN while MPS IIIA patients have a very
high level.
[0288] Purification: The biological sample (cells, tissue, blood,
serum, or the like) is homogenized and solubilized in 0.1-1.0 N
NaOH (e.g., 0.1 N, 0.2 N, 0.3 N, 0.4 N, 0.5 N, 0.6 N, 0.7 N, 0.8 N,
0.9 N, or 1.0 N) or acetic acid and then neutralized with acetic
acid or NaOH. Next a small sample is taken to measure protein
content of the sample using standard methods. 0.01-0.5 mg/mL (0.01
mg/mL, 0.07 mg/mL, 0.12 mg/mL, 0.17 mg/mL, 0.22 mg/mL, 0.27 mg/mL,
0.32 mg/mL, 0.37 mg/mL, 0.42 mg/mL, or 0.5 mg/mL) protease
(trypsin, chymotrypsin, pepsin, pronase, papain, or elastase) is
treated in 0.1-0.5 M (e.g., 0.1 M, 0.16 M, 0.23 M, 0.32 M, 0.39 M,
0.44 M, or 0.5 M) NaCl, 0.01-0.1 M (e.g., 0.01 M, 0.02 M, 0.04 M,
0.06 M, 0.08 M, 0.1 M) NaOAc, at pH 5.5-7.5 (e.g., 5.5, 6.0, 6.5,
7.0, or 7.5) and 25-40 C (e.g., 25 C, 30 C, 35 C, or 40 C) for 1-24
hours (e.g., 1 h, 2 h, 4 h, 6 h, 8 h, 12 h, 18 h, 24 h). The sample
is diluted to reduce the ionic strength and loaded onto an ion
exchange column in 5-100 mM (e.g., 5 mM, 10 mM, 20 mM, 30 mM, 40
mM, 50 mM, 60 mM, 70 mM, 75 mM, 80 mM, 90 mM, 95 mM, 100 mM) NaOAc
pH 5-7 with 0-300 mM NaCl. After washing, the bound
glycosaminoglycans are eluted with 5-100 mM NaOAc pH 5-7 (e.g., 5,
5.5, 6, 6.5, 7) with 0.8-3 M (e.g., 0.8 M, 1 M, 1.2 M, 1.4 M, 1.6
M, 1.8 M, 2 M, 2.5 M, or 3 M) NaCl. The eluted glycans are then
concentrated and desalted by ethanol precipitation, size exclusion,
or other methods. The purified glycans are dried for further
analysis.
[0289] Liberation of non-reducing end residual: The purified
glycans are resuspended in 10-300 mM sodium acetate, tris,
phosphate, or other suitable buffer, 0.02-1 mM (e.g., 0.02, 0.04,
0.06, 0.08, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, or 1)
calcium acetate, pH 5-8 (e.g., 5, 5.5, 6, 6.5, 7, 7.5, or 8), were
digested with heparin lyases I, II, III, I and II, I and III, II
and III, or I, II, and III (0.0.15-1.5 milliunits of each in 100-ul
reactions, IBEX, Montreal, Canada) at 25 to 37.degree. C. for 1 to
24 hours.
[0290] Fluorescent tagging of glycan residual: Dried glycan sample
is re-suspended in 2-100 .mu.L 0.003-0.1 M (e.g., 0.003 M, 0.003 M,
0.03 M, 0.06 M, 0.1 M) AB, AA, AMAC, or Bodipy dye and incubated at
room temperature for 1-120 minutes (e.g., 1-10 min, 10-15 min,
15-20 min, 20-25 min, 25-30 min, 30-40 min, 40-50 min, 50-60 min,
60-90 min, 90-120 min). Next, the reaction is initiated with 2-100
.mu.L (2 .mu.L, 5 .mu.L, 10 .mu.L, 15 .mu.L, 20 25 30 40 50 60 70
90 or 100 .mu.L) 1 M NaCNBH.sub.4 and the reaction is allowed to
proceed at 25-100 C. (e.g., 25 C, 30 C, 35 C, 40 C, 50 C, 60 C, 70
C, 80 C, 90 C, 100 C).
[0291] Detection of glycan residual: HPLC separation of tagged
saccharides was performed utilizing the following conditions:
Column types: 130A BEH particle Phenyl (1.7, 2.5, 3.5, 5, or 10 uM
particle size), 130A BEH particle C18 (1.7, 2.5, 3.5, 5, or 10 uM
particle size), HSS particle C18 (1.8, 3.5, or 5 uM particle size),
or 300 A BEH particle C18 (1.7, 3.5, 5, 10 uM particle size) with
suitable length and internal diameter.
[0292] Buffer Conditions:
A=Ammonium Acetate, Sodium Acetate, or Sodium Chloride (e.g., 0 M,
10 mM, 20 mM, 30 mM, 40 mM, 100 mM, 500 mM, 1 M, 2 M) with 0-20%
methanol B=100% Alcohol, such as methanol, ethanol, or
isopropanol
Initial Conditions: 70-95% A, 0-30% B
[0293] Flow Rate is constant at 0.05-1 ml/min Runs a gradient down
to 70-90% A, 10-30% B over 5-65 min. At 8.1 min runs a gradient to
0-20% A, 80-100% B over 5-20 min. 5-65 min returns to initial
conditions
[0294] FIG. 1 illustrates an HPLC trace of eluted compounds
detected in normal patient urine not subject to enzymatic glycan
residual liberation (i.e., providing background signals). FIG. 2
illustrates an HPLC trace of eluted compounds detected in normal
patient urine subject to enzymatic glycan residual liberation as
set forth in Example 1. FIG. 3 illustrates an HPLC trace of eluted
compounds detected in MPS IIIA patient urine not subject to
enzymatic glycan residual liberation (i.e., providing background
signals). FIG. 4 illustrates an HPLC trace of eluted compounds
detected in MPS IIIA patient urine subject to enzymatic glycan
residual liberation.
Example 2
[0295] The processes described in Example 1 are repeated and/or
modified for the diseases listed in Tables 1-4 utilizing the
enzymes described there in and detecting the glycan residual
compounds also described therein.
Example 3: NRE Analysis of MPS I, II, VI and VII Cells
[0296] To demonstrate the potential utility of this approach,
dermal fibroblasts from human MPS I patients (.alpha.-iduronidase
[IDUA] deficiency) and from normal human donors were grown. Cells
were expanded and kept in culture up to 8 weeks to allow for
significant lysosomal accumulation. GAGs remaining in the cell
layer were extracted and subjected to enzymatic depolymerization
followed by reductive amination with [.sup.12C.sub.6]aniline.
Samples were mixed with 10 pmoles of each [.sup.13C.sub.6]aniline
unsaturated disaccharide standard and
[.sup.13C.sub.6]aniline-tagged I0S0 that was synthesized. All
possible candidate structures were searched for (FIG. 6) and the
extracted ion chromatogram shown in FIG. 7a. Peaks 1-7 comigrated
with known unsaturated disaccharides and had the expected m/z
values. The MPS I sample had an additional peak marked by an
asterisk that was not present in the normal fibroblast sample. This
peak had the same elution position as the aniline-tagged I0S0
standard (expanded inset in FIG. 7a). The mass spectrum for this
peak gave an m/z=511.1 and isotopic cluster consistent with the
proposed structure I0S0, and a corresponding m/z=517.1 and isotopic
cluster expected for the [.sup.13C.sub.6]aniline tagged standard
(FIG. 7b). Further verification was carried out by
collision-induced dissociation (CID), which demonstrated structural
identity with the I0S0 standard (FIG. 10). Digestion of heparan
sulfate from cells derived from MPS I patients also yielded a
disaccharide of m/z=591.1 (FIG. 11a), consistent with the structure
10S6. This material comigrated with the internal disaccharide D2S0
and thus was contained within peak 6 in the chromatogram shown in
FIG. 7a. However, it was easily discriminated from D2S0 by the mass
detector given the 18 amu difference. Pretreatment of an MPS I
sample with .alpha.-L-iduronidase led to the loss of the native NRE
structures confirming their identity (FIG. 12). Fibroblasts from
three different MPS I patients exhibited NRE species identified as
I0S0 and 10S6. These entities were not observed in samples prepared
from normal human fibroblasts.
[0297] MPS II (idurono-2-sulfatase [IDS] deficiency) and MPS VII
(.beta.-D-glucuronidase [GLCA] deficiency) also affect heparan
sulfate degradation due to defects in processing the non-reducing
terminal uronic acid (desulfation of iduronate-2-sulfate and
removal of glucuronic acid, respectively). Saturated NRE
disaccharides were detected after digestion of GAGs derived from
fibroblasts of MPS II and MPS VII patients (FIG. 6 and FIGS. 11b
and 11c). The mass spectra for the MPS II NREs and their elution
positions were consistent with the expected disaccharide biomarkers
12S0 and 12S6. Analysis of MPS VII heparan sulfate was more
complex, yielding four disaccharides tentatively identified as
G0A0, G0A6, G0S0 and G0S6. Treatment of the MPS II samples with
recombinant IDS converted the NRE to those found in MPS I (I0S0 and
10S6, respectively; FIG. 13).
[0298] MPS I, MPS II, and MPS VII also affect the degradation of
chondroitin sulfate and dermatan sulfate. Analysis of these GAGs
using chondroitinase ABC yielded a set of NRE disaccharides
diagnostic for each disorder (FIG. 6). MPS I yielded the
monosulfated NRE disaccharides I0a4 and I0a6 in addition to the
disulfated disaccharide I0a10 (FIG. 11d). MPS II yielded I2a4 and
I2a6 (FIG. 11e) and MPS VII yielded G0a0, G0a4, G0a6 and G0a10
(FIG. 11f).
[0299] Analysis of chondroitin sulfate and dermatan sulfate from
MPS VI (N-acetylgalactosamine 4-sulfatase [G4S] deficiency)
demonstrated accumulation of N-acetylgalactosamine-4-sulfate (a4,
FIG. 6), which co-migrated with an aniline tagged a4 standard (FIG.
14). Note that a4 resolves partially by liquid chromatographically
from 6-sulfo-N-acetylgalactosamine (a6) (lower panel). However, the
biological sample yielded predominantly a4, consistent with the
deficiency in the N-acetylgalactosamine 4-sulfatase in these cells.
No trisaccharides species were detected.
Example 4: NRE Analysis of MPS III Cells
[0300] The Sanfilippo family of MPS disorders was analyzed using
the same approach as above: MPS IIIA (sulfamidase [SGSH]
deficiency), MPS IIIB (.alpha.-N-acetylglucosaminidase [NAGLU]
deficiency), MPS IIIC (N-acetyltransferase [HGSNAT] deficiency) and
MPS IIID (glucosamine-6-sulfatase [GNS] deficiency). These
disorders only affect lysosomal degradation of heparan sulfate and
have in common deficiencies in the enzymes that process the NRE
glucosamine residue. Because heparin lyases cleave linkages between
a glucosamine unit and a uronic acid, it was expected that analysis
of Sanfilippo heparan sulfate should yield diagnostic
monosaccharides (glucosamine derivatives) or trisaccharides
(glucosamine-uronic acid-glucosamine derivatives) from the NRE as
opposed to the disaccharides observed in MPS I, II and VII.
[0301] Analysis of MPS IIIA samples showed the typical unsaturated
disaccharides generated from internal segments of the chains and a
unique peak at 38.5 minutes not present in control or other MPS
samples. This material had the characteristic mass spectrum
expected for [.sup.12C.sub.6]aniline-tagged N-sulfoglucosamine (S0,
m/z=335.1) and comigrated with an authentic
[.sup.13C.sub.6]aniline-tagged standard (m/z=341.1; FIG. 7c,
inset). Treatment of two different MPS IIIA samples with
sulfamidase prior to heparinase depolymerization destroyed the S0
biomarker, consistent with its proposed identity (FIG. 15).
Digestion of MPS IIIA heparan sulfate also yielded trisaccharides
that varied in the number of acetate and sulfate groups (FIG. 7c,
dp3). The most prominent species dp3(0Ac,3S) was analyzed by CID
and gave a fragmentation pattern consistent with S0U2S0 (FIG. 16a).
Although the uronic acid could be glucuronic acid, iduronic acid
predominates in segments of the chain containing repeating
N-sulfoglucosamine units.
[0302] Analysis of MPS IIIB samples yielded three NRE
trisaccharides, with m/z values consistent with the presence of 1-2
acetate groups and 1-3 sulfates (FIG. 7d). Since MPS IIIB is
characterized by the lack of .alpha.-N-acetylglucosaminidase, the
terminal sugar should be N-acetylglucosamine, which was confirmed
by CID analysis of the predominant trisaccharide (m/z=794)
identified as A0U2S0 (FIG. 16b). Similarly, the NREs from MPS IIIC
were predicted to contain a free unsubstituted amine due to the
deficiency of glucosamine N-acetyltransferase. Four trisaccharides
were detected, all lacking acetate groups (FIG. 7e). CID analysis
of dp3(0Ac,3S) and derivatization with propionyl anhydride
suggested structures consistent with H6U0S6 or H0U2S6 (FIG.
16c).
[0303] MPS IIID cells lack the 6-sulfatase that can remove the
6-O-sulfate group from terminal N-acetylglucosamine units. NRE
analysis of MPS IIID heparan sulfate detected a single
monosaccharide species with m/z value of 335 corresponding to
N-unsubstituted GIcNH.sub.26S (H6) (FIG. 70. While H6 is isobaric
with S0 found in MPS IIIA, its retention time was significantly
less due to the presence of the unsubstituted amine and
consequently these markers were easily discriminated. Furthermore,
H6 in MPS IIID co-eluted with [.sup.13C.sub.6]aniline-labeled
standard H6 verifying its identity (FIG. 7f, inset). No
N-acetylglucosamine-6-sulfate was detected, nor were any
trisaccharide NRE species bearing a non-reducing terminal
6-O-sulfated N-acetylglucosamine unit (FIG. 7f).
Example 5: Use of NRE Biomarkers
[0304] Although most MPS GAG samples yielded multiple NRE
carbohydrates (FIG. 6), it was possible to select single unique
NREs as biomarkers for each MPS disorder and then combine them into
a decision tree based on size of NRE structures (mono-, di- and
trisaccharides), degree of sulfation, and retention time during
liquid chromatography (FIG. 8). The diagnostic decision tree
becomes even more robust by inclusion of other carbohydrate
biomarkers (FIG. 6), but the specific NREs indicated in FIG. 8 are
sufficient to diagnose the eight MPS disorders. To determine the
potential utility of these markers for diagnosis, nine different
human urine samples from normal control subjects and patients
suffering from various Sanfilippo disorders were screened as well
as two canine urine samples (one normal and one with MPS I) and
liver, brain and kidney GAGs from MPS IIIB mice. Using the scheme
outlined in FIG. 8 all samples were correctly diagnosed (Table
16).
[0305] Table 16. Analysis of GAG samples purified from mouse
tissues and human and canine urine. GAG was extracted and analyzed
for MPS diagnostic biomarkers using the scheme shown in FIG. 8.
Diagnostic markers: MPS I, I0S0; MPS II, I2S6; MPS IIIA, S0 and
S0U2S0; MPS IIIB, A0U2S0; MPS IIIC dp3(0Ac,3S0.sub.4), a
trisaccharide containing no acetate groups and three sulfate
groups; MPS IIID, H6; MPS VI, a4; MPS VII, G0S0.
TABLE-US-00016 TABLE 16 NRE Biomarkers Sensi-Pro Sample Sample
Identity Detected Analysis Liver, Mouse-1 Unaffected, MPS IIIB
Trace Normal Carrier (Het) Liver, Mouse-2 MPS IIIB A0U2S0 MPSIIIB
Brain, Mouse-1 Unaffected, MPS IIIB Trace Normal Carrier (Het)
Brain, Mouse-2 MPS IIIB A0U2S0 MPSIIIB Kidney, Mouse-1 MPS IIIB
A0U2S0 MPSIIIB Urine, Human-1 Normal Trace Normal Urine, Human-2
Normal Trace Normal Urine, Human-3 Normal Trace Normal Urine,
Human-4 Normal Trace Normal Urine, Human-5 MPS IIIC dp3
(0Ac,3S0.sub.4) MPSIIIC Urine, Human-6 MPS IIIC dp3 (0Ac,3S0.sub.4)
MPSIIIC Urine, Human-7 MPS IIIC dp3 (0Ac,3S0.sub.4) MPSIIIC Urine,
Human-8 MPS IIIA S0, S0U2S0 MPSIIIA Urine, Human-9 MPS IIIB A0U2S0
MPSIIIB Urine, Canine-1 Unaffected, MPS I Trace Normal Carrier
(Het) Urine, Canine-2 MPS I I0S0 MPS I
[0306] Analysis of multiple MPS IIIA cell lines showed striking
accumulation of the S0 biomarker, which corresponded well with the
level of heparan sulfate storage (Table 17). Normal fibroblasts
yielded minute amounts of S0. In general, samples from normal
cells, tissues and urine exhibited less than 1% of the amount of
NRE biomarkers observed in samples from affected patients or
animals.
TABLE-US-00017 TABLE 17 Quantitation of markers in MPS IIIA cells
and normal fibroblasts Enzyme activity Heparan Sulfate MPS IIIA
marker: S0 Cell line (Units/mg) (nmol/mg cell protein) (pmol/mg
cell protein) Normal 9 .+-. 0.7 0.59 .+-. 0.22 2 .+-. 2 GM00629
0.49 .+-. 0.12 33.6 670 GM00643 0.45 .+-. 0.08 28.4 720 GM00879
0.62 .+-. 0.02 17.3 490 GM00934 0.46 .+-. 0.07 16.6 470 GM06110
0.55 .+-. 0.36 6.8 220
[0307] Five normal fibroblasts were analyzed (CRL-1634 (human
foreskin fibroblasts), GM00200 (clinically unaffected sibling of
metachromatic leukodystrophy patient), GM05659, GM08398, and
GM15871 (clinically unaffected sibling of an Ehlers-Danlos
patient). The average values.+-.standard deviation are provided.
The values for the various MPS IIIA lines represent duplicate
analyses for enzyme activity and single determinations for heparan
sulfate storage and the S0 biomarker.
[0308] The detection of lysosomal storage based on GAG content in
the brain and urine has been challenging due to various methods
used for detection and quantitation, in particular indirect
techniques based on dye binding or displacement. Urine and brain
samples from MPS IIIA (Sgsh.sup.-/-) and wildtype mice and MPS IIIA
human fibroblasts were analyzed using the scheme described in FIG.
8. Using this method, total heparan sulfate and the biomarker S0
showed a 12-fold accumulation in MPS IIIA urine samples compared to
the wildtype (FIG. 9a). The trisaccharide biomarker S0U2S0 was
readily detectable in the Sgsh.sup.-/- urine, but virtually
undetectable in wildtype urine. In brain samples the heparan
sulfate level was elevated 12-fold, whereas the biomarker S0
increased 60-fold compared to the wildtype (FIG. 9b). The
trisaccharide marker was essentially present only in the
Sgsh.sup.-/- sample.
[0309] In order to test whether the NRE structures afford a more
precise and sensitive assay to monitor therapeutic enzyme
replacement, cultures of MPS IIIA human fibroblasts were
supplemented with recombinant sulfamidase for 48 hours prior to GAG
extraction and analysis. Enzyme replacement led to a significant
drop in heparan sulfate and both the biomarkers, S0 and S0U2S0
(FIG. 9c). Thus, the NRE biomarkers, in particular the
trisaccharides, are useful for monitoring the therapeutic efficacy
of intervention strategies.
Example 6: Synthesis of I0S0
[0310] All moisture sensitive reactions were performed under an
argon atmosphere by using vacuum dried glassware. All commercial
materials were used without purification, unless otherwise noted.
CH2Cl.sub.2 was freshly distilled from calcium hydride under
nitrogen prior to use. Toluene, DMF, diethylether, methanol and THF
were purchased anhydrous and used without further purification.
Molecular sieves (4 .ANG.) were flame activated in vacuo prior to
use. All reactions were performed at room temperature unless
specified otherwise. TLC analysis was conducted on Silica gel 60
F254 (EMD Chemicals Inc.) with detection by UV-absorption (254 nm)
when applicable, and by spraying with 20% sulfuric acid in ethanol
followed by charring at -150.degree. C. or by spraying with a
solution of (NH.sub.4).sub.6Mo.sub.7O.sub.24H.sub.2O (25 g/L) in
10% sulfuric acid in ethanol followed by charring at -150.degree.
C. Column chromatography was performed on silica gel G60
(Silicycle, 60-200 60 .ANG.) or on Bondapak C-18 (Waters). .sup.1H
and .sup.13C NMR spectra were recorded on Varian inova-300 (300/75
MHz), inova-500 (500/125 MHz) and inova-600 (600/150 MHz)
spectrometers equipped with sun workstations. Chemical shifts are
reported in parts per million (ppm) relative to tetramethylsilane
(TMS) as the internal standard. NMR data is presented as follows:
Chemical shift, multiplicity (s=singlet, d=doublet, t=triplet,
dd=doublet of doublet, m=multiplet and/or multiple resonances),
coupling constant in Hertz (Hz), integration. All NMR signals were
assigned on the basis of .sup.1H NMR, .sup.13C NMR, COSY and HSQC
experiments. Mass spectra were recorded on an Applied Biosystems
5800 MALDI-TOF proteomics analyzer. The matrix used was
2,5-dihydroxy-benzoic acid (DHB) and Ultramark 1621 as the internal
standard.
[0311] The synthesis of
.beta.-D-idopyranosyluronate)-(1.fwdarw.4)-(2-N-sulfoamino-2-deoxy-.alpha-
./.beta.-D-glucopyranoside) (7) (I0S0) is described below:
##STR00003##
[0312] Benzyl
(2-O-acetyl-3-O-benzyl-4,6-O-benzylidene-.beta.-D-glucopyranosyl)-(1.fwda-
rw.4)-6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-.alpha./.beta.-D-glucopyranosi-
de (3): Glycosyl donor 1 (467 mg, 1.05 mmol) and glycosyl acceptor
2 (877 mg, 0.375 mmol) were combined in a flask, co-evaporated with
toluene (3.times.3 mL), and dissolved in DCM (8.7 mL). Powdered
freshly activated 4 .ANG. molecular sieves were added, and the
mixture was stirred for 30 min at ambient temperature. The reaction
mixture was cooled (0.degree. C.) and NIS (0.236 g, 1.052 mmol) and
TMSOTf (19.08 .mu.L, 0.105 mmol) were added and the stirring was
continued until TLC indicated the consumption of donor (.about.10
min). The mixture was then quenched with aqueous
Na.sub.2S.sub.2O.sub.3 and extracted with DCM (2.times.10 mL). The
combined organic layers were dried (MgSO.sub.4) and filtered and
the filtrate was concentrated in vacuo. The residue was purified by
silica gel chromatography using stepwise gradient of toluene and
EtOAc (100-80%) to give disaccharide 3 (658 mg, 73%). .sup.1H NMR
(500 MHz, CDCl.sub.3): .delta. 7.44-7.25 (m, 30H, CH Aromatic),
5.28 (s, 2H, CH benzylidene.times.2), 5.00-4.96 (m, 4H, H2, H'1,
H1.alpha., H'2 CHH Bn), 4.92 (d, 1H, J=11.5 Hz, CHH Bn), 4.84 (d,
1H, J=11.0 Hz, CHH Bn), 4.80 (d, 1H, J=11.0 Hz, CHH Bn), 4.76-4.55
(m, 10H, CHH Bn.times.4, CHH Bn.times.2, CHH Bn.times.2,
H6b.alpha.,.beta.), 4.45 (dd, 1H, J=2.0 Hz, J=12.5 Hz, H6a.alpha.),
4.35 (d, 1H, J=8.0 Hz, H1.beta.), 4.14 (t, 1H, J=3.5 Hz, H5a), 4.11
(t, 1H, J=4.0 Hz, H6.beta.), 3.91-3.75 (m, 3H, H'5, H'4, H4.beta.),
3.71 (bs, 1H, H'3), 3.51 (m, 1H, H2.beta.), 3.44-3.42 (m, 2H,
H5.beta., H2.alpha.), 3.25 (t, 1H, J=9.5 Hz, H3.beta.), 3.19 (d,
1H, J=11.0 Hz, H'6b), 3.10 (d. 1H, J=11.5 Hz, H'6a). .sup.13C NMR
(75.5 MHz, CDCl.sub.3): .delta. 170.4, 170.2, 138.1, 137.9, 137.6,
128.9, 128.4, 128.3, 128.0, 127.9, 127.9, 127.6, 127.4, 127.1,
126.1, 100.4, 98.0, 97.0, 81.2, 77.4, 77.0, 76.5, 75.0, 74.9, 73.8,
73.7, 73.5, 72.1, 69.0, 69.0, 67.1, 62.3, 60.3, 33.9, 24.8, 20.9,
20.8, 19.9, 19.8, 18.4, 18.3, -2.1, -3.3. HRMS-MALDI: (M+Na.sup.+)
calcd for C.sub.44H.sub.47N.sub.3O.sub.12, 809.3159. found
809.3155.
[0313] Benzyl (methyl
2-O-acetyl-3-O-benzyl-.beta.-D-idopyranosyluronate)-(1.fwdarw.4)-(6-O-ace-
tyl-2-azido-3-O-benzyl-2-deoxy-.alpha./.beta.-D-glucopyranoside)
(4): To a solution of disaccharide 3 (0.633 g, 0.781 mmol) in DCM
was added ethanethiol (0.345 mL, 4.68 mmol) and p-TsOH (29.6 mg,
0.156 mmol). The resulting reaction mixture was stirred at ambient
temperature for 1 h. The reaction mixture was quenched with
Et.sub.3N and concentrated in vacuo. The residue was purified by
silica gel column chromatography using a stepwise gradient of
toluene and EtOAc (100-80%) to give pure diol (0.543 g, 96%). To a
vigorously stirred solution of the diol (0.533 g, 0.738 mmol) in a
mixture of DCM:H.sub.2O (0.15 M, 2/1, v/v) was added TEMPO (22.96
mg, 0.147 mmol) and BAIB (0.594 g, 1.845 mmol). Stirring was
continued until TLC indicated complete conversion of the starting
material to a spot of lower R.sub.f (.about.45 min). The reaction
mixture was quenched with aqueous Na.sub.2S.sub.2O.sub.3 and the
resulting mixture was extracted with EtOAc (2.times.10 mL), and the
combined organic layers were dried (MgSO.sub.4) and filtered, and
the filtrate was concentrated in vacuo. The oily residue was
dissolved in THE (0.1 M) and treated with excess of freshly
prepared ethereal solution of diazomethane until the reaction
mixture stayed yellow. The excess diazomethane was quenched by the
addition of AcOH until the mixture became colorless. The mixture
was concentrated in vacuo and the residue co-evaporated with
toluene. The residue was purified by silica gel column
chromatography using stepwise gradient of toluene EtOAc (100-50%)
to give compound 4 (0.34 g, 83%, 2 steps). .sup.1H NMR (500 MHz,
CDCl3): .delta. 7.39-7.15 (m, 30H, CH Aromatic), 5.06 (bs, 2H,
H'1), 4.98 (d, 1H, J=3.5 Hz, H1.alpha.), 4.92-4.88 (m, 3H, H'2,
H'5, CHH Bn), 4.74-4.58 (m, 7H, CHH Bn.times.4, CHH Bn.times.3),
4.50 (dd, 2H, J=1.5 Hz, 12.0 Hz, H6b.alpha., H6b.beta.), 4.36 (d,
1H, J=12.5 Hz, H6a.alpha.), 4.31 (d, 1H, J=8.0 Hz, H1.beta.),
4.22-4.18 (m, 2H, H5.alpha., H6a.beta.), 3.96 (bt, 1H, J=10.0 Hz,
H'4), 3.88-3.85 (m, 3H, H3.alpha., H4.alpha., H4.beta.), 3.71 (d,
2H, J=2.5 Hz, H'3), 3.49-3.47 (m, 1H, H2.beta.), 3.45 (s, 3H,
CO.sub.2CH.sub.3), 3.41-3.36 (m, 2H, H2.alpha., H5.beta.), 3.25 (t,
1H, J=9.5 Hz, H3.beta.), 2.10 (s, 3H, CH.sub.3 Ac), 2.06 (s, 3H,
CH.sub.3 Ac). .sup.13C NMR (75.5 MHz, CDCl.sub.3): .delta. 170.5,
170.5, 169.4, 169.3, 169.1, 137.8, 137.7, 137.1, 136.4, 128.9,
128.5, 128.4, 128.1, 128.1, 128.0, 127.8, 127.4, 127.3, 127.3,
125.2, 100.2, 97.9, 96.6, 81.1, 78.4, 77.4, 77.0, 76.6, 75.0, 74.6,
74.4, 74.3, 74.3, 73.1, 72.2, 70.8, 69.8, 69.3, 68.4, 67.6, 67.1,
67.0, 66.2, 63.4, 62.0, 51.9, 20.8. HRMS-MALDI: (M+Na.sup.+) calcd
for C.sub.38H.sub.43N.sub.3O.sub.13, 749.2795. found 749.2790.
[0314] Benzyl
(3-O-benzyl-(3-D-idopyranosyluronate)-(1.fwdarw.4)-(2-azido-3-O-benzyl-2--
deoxy-.alpha./.beta.-D-glucopyranoside) (5): To a solution of
compound 4 (70 mg, 0.09 mmol) in THF (1.4 mL) was added LiOH (0.4
mL, 0.1 M) at room temperature. Stirring was continued for 40 min,
after which the reaction mixture was brought to pH 9.0 by the
addition of aqueous HCl (1.0 M), the resulting mixture was
concentrated in vacuo and the residue was purified by column
chromatography over latrobeads using a stepwise gradient of toluene
and methanol (100-70%). Appropriate fractions were concentrated in
vacuo, to provide compound 5 (60 mg, 99%). .sup.1H NMR (500 MHz,
CD.sub.3OD): .delta. 7.44-7.23 (m, 30H, Aromatic), 5.04-4.98 (m,
4H, H1.alpha., CHH Bn, CHH Bn), 4.94 (d, 2H, J=12.0 Hz, CHH Bn),
4.92-4.75 (m, 3H, CHH Bn, CHH Bn, CHH Bn), 4.70 (d, 1H, J=12.0 Hz,
CHH Bn), 4.63 (t, 2H, J=10.5 Hz, CHH Bn, CHH Bn), 4.58 (d, 1H,
J=12.0 Hz, CHH Bn), 4.44 (d, 1H, J=8.0 Hz, H1.beta.), 4.41 (dd, 2H,
J=4.5 Hz, J=19.0 Hz, H6b.alpha., H'5), 4.12 (t, 1H, J=9.5 Hz,
H4.alpha.), 4.04 (t, 1H, J=9.5 Hz, H4.beta.), 3.98-3.79 (m, 5H,
H6a,b.beta., H6a.alpha., H5.alpha., H3.alpha.), 3.57-3.52 (m, 4H,
H'2.times.2, H'3.times.2), 3.46-3.43 (m, 2H, H3.beta., H5.beta.),
3.39-3.35 (m, 2H, H2.alpha., H2.beta.). .sup.13C NMR (75.5 MHz,
CD.sub.3OD): .delta. 176.7, 140.2, 140.0, 138.7, 129.3, 129.2,
129.0, 128.3, 101.9, 101.3, 101.2, 98.2, 82.5, 82.2, 82.0, 79.4,
77.5, 77.0, 76.6, 76.0, 75.7, 75.0, 74.9, 73.8, 73.3, 73.0, 72.8,
72.4, 72.2, 71.9, 70.5, 67.9, 64.3, 62.2, 62.1, 49.9, 49.7, 49.4,
49.1, 48.8, 48.5, 48.2; HRMS-MALDI: (M+Na.sup.+) calcd for
C33H37N3011, 651.2428. found 651.2422.
[0315] Benzyl
(3-O-benzyl-.beta.-D-idopyranosyluronate)-(1.fwdarw.4)-(2-N-sulfoamino-3--
O-benzyl-2-deoxy-.alpha.-D-glucopyranoside) (6): To a solution of
compound 5 (20 mg, 0.03 mmol) in THF (2 mL) was added 1.0 M
solution of PM.sub.3 in THF (0.24 mL, 0.24 mmol) and NaOH (0.1 M,
3.0 mL, 0.3 mmol). The reaction mixture was stirred at room
temperature for 1 h and the progress of the reaction was followed
by TLC (H.sub.2O/acetonitrile, 10/90, v/v). The presence of the
amino group was indicated using ninhydrin as visualizing agent.
After the completion of the reaction, pH was adjusted to 9.0 by
careful addition of aqueous HCl (0.1 M). The mixture was
concentrated in vacuo and the residue co-evaporated with toluene.
To a solution of the crude residue in anhydrous methanol (5.0 mL)
was added pyridinium sulfur trioxide (23.8 mg, 0.15 mmol), and
triethylamine (1.5 mL, 0.30 mmol) and sodium hydroxide (0.6 mL,
0.06 mmol). Stirring was continued at room temperature for 1 h
until RP-018 TLC (H.sub.2O/methanol, 60/40, v/v) indicated the
disappearance of the starting material. The mixture was
co-evaporated with toluene in vacuo and dissolved in H.sub.2O and
passed through a short column of Bio-Rad 50.times.8 Na.sup.+ resin
(0.6.times.2.5 cm). The residue was applied to a small RP-018
column, which was eluted with a stepwise gradient of water and
methanol (90/10 to 60/40, v/v). The appropriate fractions were
lyophilized to give compound 6 (15 mg, 66%). .sup.1H NMR (500 MHz,
CD.sub.3OD): .delta. 7.53-7.23 (m, 15H, CH Aromatic), 5.38 (d, 1H,
J=3.5 Hz, H1.alpha.), 4.96 (d, 1H, J=4.5 Hz, H'1), 4.92 (d, 1H,
J=10.5 Hz, CHH Bn), 4.87-4.73 (m, 5H, CHH Bn, CHH Bn, CHH Bn, CHH
Bn, CHH Bn), 4.59 (d, 1H, J=11.0 Hz, CHH Bn), 4.46 (bs, 1H, H'5),
4.01-3.99 (M, 2H, H'4, H4.alpha.), 3.85-3.83 (m, 2H, H6a,b), 3.74
(bd, 1H, J=9.5 Hz, H5.alpha.), 3.68 (t, 1H, J=10 Hz, H3a), 3.56 (m,
3H, H2.alpha., H'2, H'3). .sup.13C NMR (75.5 MHz, D.sub.2O):
.delta. 176.8, 140.1, 139.53, 129.4, 129.4, 129.2, 129.1, 129.0,
128.5, 128.3, 102.5, 100.5, 80.1, 79.9, 78.1, 74.6, 73.9, 73.5,
72.2, 71.7, 71.6, 71.1, 63.4, 58.2, 49.8, 49.5, 49.3, 49.0, 48.7,
48.4, 48.1.
[0316]
.beta.-D-idopyranosyluronate)-(1.fwdarw.4)-(2-N-sulfoamino-2-deoxy--
.alpha./.beta.-D-glucopyranoside) (7): Pd/(OH).sub.2 on carbon
(Degussa type, 20%, 1.5 times the weight of starting material) was
added to the solution of compound 6 (4 mg, 6 .mu.mol) in tBuOH and
H.sub.2O (1/1, v/v, 2 mL) and then placed under an atmosphere of
hydrogen. The reaction was completed after 16 h indicated by C18
TLC (H.sub.2O/acetonitrile, 10/90, v/v). The mixture was filtered
through Celite and the filtrate was concentrated in vacuo. The
residue was re-dissolved in water and then passed through a short
column of Bio-Rad 50.times.8 Na.sup.+ resin (0.6.times.2.5 cm)
using H.sub.2O as eluent. Appropriate fractions were lyophilized to
provide compound 7 (2 mg, 83%). .sup.1H NMR (500 MHz, D.sub.2O),
.alpha.-anomer: .delta. 5.45 (d, 1H, J=3.5 Hz, H1.alpha.), 4.81 (t,
2H, J=6.0 Hz, H'1), 4.52 (t, 2H, J=4.5 Hz, H'5), 3.94-3.85 (m, 1H,
H5.alpha.), 3.84-3.80 (m, 3H, H'4, H6a,b), 3.74-3.61 (m, 3H,
H3.alpha., H4a, H'3), 3.47-3.44 (m, 1H, H'2), 3.26 (dd, 1H, J=3.5
Hz, J=10.0 Hz, H2.alpha.); .sup.13C NMR (150 MHz, D.sub.2O):
.delta. 176.6, 101.2, 91.2, 78.2, 72.7, 71.7, 71.3, 70.5, 69.6,
60.2, 58.2.
* * * * *