U.S. patent application number 16/152516 was filed with the patent office on 2019-08-29 for glycoconjugates of rna interference agents.
The applicant listed for this patent is ALNYLAM PHARMACEUTICALS, INC.. Invention is credited to Andrea FORST, Philipp HADWIGER, Hans-Peter VORNLOCHER.
Application Number | 20190264203 16/152516 |
Document ID | / |
Family ID | 39876191 |
Filed Date | 2019-08-29 |
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United States Patent
Application |
20190264203 |
Kind Code |
A1 |
FORST; Andrea ; et
al. |
August 29, 2019 |
GLYCOCONJUGATES OF RNA INTERFERENCE AGENTS
Abstract
The present invention relates to agents, compositions and
methods for inhibiting the expression of a target gene, comprising
an RNAi agent bearing at least one galactosyl moiety. These are
useful for delivering the gene expression inhibiting activity to
cells, particularly hepatocytes, and more particularly in
therapeutic applications.
Inventors: |
FORST; Andrea; (Bayreuth,
DE) ; HADWIGER; Philipp; (Kulmbach, DE) ;
VORNLOCHER; Hans-Peter; (Bayreuth, DE) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
ALNYLAM PHARMACEUTICALS, INC. |
Cambridge |
MA |
US |
|
|
Family ID: |
39876191 |
Appl. No.: |
16/152516 |
Filed: |
October 5, 2018 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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14500356 |
Sep 29, 2014 |
10131907 |
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16152516 |
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12108253 |
Apr 23, 2008 |
8877917 |
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14500356 |
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60925880 |
Apr 23, 2007 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
C12N 2310/321 20130101;
C12N 2310/14 20130101; C12N 2310/315 20130101; A61K 47/60 20170801;
C12N 2310/351 20130101; A61K 47/549 20170801; A61K 31/713 20130101;
C12N 15/111 20130101; C12N 2320/32 20130101; C12N 15/113
20130101 |
International
Class: |
C12N 15/113 20060101
C12N015/113; A61K 31/713 20060101 A61K031/713; A61K 47/54 20060101
A61K047/54; A61K 47/60 20060101 A61K047/60; C12N 15/11 20060101
C12N015/11 |
Claims
1-20. (canceled)
21. An RNAi agent for inhibiting the expression of a target gene in
a cell, wherein the RNAi agent consists essentially of two mutually
complementary oligoribonucleotide strands of between 15 and 30
nucleotides in length, wherein an ASGPR ligand comprising at least
two galactose moieties is conjugated to at least one of the
oligoribonucleotide strands via a branched linker and via a
phosphate or phosphate modification at the 5' end, and wherein at
least one oligoribonucleotide strand is complementary to at least
one portion of a mRNA corresponding to the target gene.
22. The RNAi agent of claim 21, wherein the ASGPR ligand conjugated
to the oligoribonucleotide through the branched linker has a
structure of formula (III) ##STR00021## wherein Z.sup.3 and Z.sup.4
are independently O or S; and the ASGPR ligand is linked to O via
at least one linker group ##STR00022## wherein Z.sup.1 and Z.sup.2
are independently O or S, and n is 1-20.
23. The RNAi agent of claim 22, wherein at least one of Z.sup.3 and
Z.sup.4 is S.
24. The RNAi agent of claim 22, wherein both of Z.sup.3 and Z.sup.4
are O.
25. The RNAi agent of claim 21, wherein the ASGPR ligand is linked
to the branched linker through an intervening linker.
26. The RNAi agent of claim 25, wherein the ASGPR ligand linked to
the branched linker through the intervening linker has a structure
of formula (IV) ASGPR
ligand-O--CH.sub.2CH.sub.2(OCH.sub.2CH.sub.2).sub.nOP(Z.sup.5)(Z.sup.6)-b-
ranched-linker Formula (IV) wherein n is 1-20; and Z.sup.5 and
Z.sup.6 are each independently O or S.
27. The RNAi agent of claim 26, wherein n is 3.
28. The RNAi agent of claim 26, wherein at least one of Z.sup.5 and
Z.sup.6 is S.
29. The RNAi agent of claim 26, wherein both of Z.sup.5 and Z.sup.6
are O.
30. The RNAi agent of claim 21, wherein the galactose moieties are
N-acetylgalactosamine moieties.
31. The RNAi agent of claim 30, wherein the distance between the
N-acetylgalactosamine moieties is at least 4 .ANG..
32. The RNAi agent of claim 21, wherein the 5' end phosphate
modification is characterized by replacing one or both non-bridging
oxygen atoms of the phosphate by B, C, N, or a group containing
thereof; S; Se; H; or OR, wherein R is alkyl or aryl.
33. The RNAi agent of claim 21, wherein the 5' end phosphate
modification is characterized by replacing one or both bridging
oxygen atoms of the phosphate by C, N, or a group containing
thereof; or S.
34. The RNAi agent of claim 21, wherein the 5' end phosphate
modification is selected from the group consisting of
phosphorothioate, phosphoroselenates, borano phosphates, borano
phosphate esters, hydrogen phosphonates, phosphoroamidates,
alkylene or arylene phosphonates, and phosphotriesters.
35. The RNAi agent of claim 21, wherein the RNAi agent is capable
of inhibiting the expression of the target gene in the cell.
36. The RNAi agent of claim 35, wherein the cell harbors an
asialoglycoprotein receptor on its surface.
37. The RNAi agent of claim 36, wherein the cell is a
hepatocyte.
38. A pharmaceutical composition, comprising (i) an RNAi agent of
claim 1; and (ii) a pharmaceutically acceptable excipient.
39. A method for the manufacture of an RNAi agent of claim 1,
comprising the steps of (i) synthesizing two mutually complementary
oligoribonucleotide strands of between 15 and 30 nucleotides in
length, wherein at least one of the oligoribonucleotides is coupled
to a ligand comprising a linker group and at least one galactose
moiety; and (ii) effecting the hybridization of the at least two
mutually complementary oligoribonucleotides.
40. The method of claim 39, further comprising the step of
formulating the RNAi agent with a pharmaceutically acceptable
excipient.
Description
RELATED APPLICATIONS
[0001] This application is a continuation of U.S. patent
application Ser. No. 14/500,356, filed Sep. 29, 2014, which is a
continuation of U.S. patent application Ser. No. 12/108,253, filed
Apr. 23, 2008, now U.S. Pat. No. 8,877,917, which claims the
benefit of priority to U.S. Provisional Patent Application Ser. No.
60/925,880, filed Apr. 23, 2007; the entirety of which are hereby
incorporated by reference.
FIELD OF THE INVENTION
[0002] The present invention relates to agents, compositions and
methods for inhibiting the expression of a target gene, comprising
an RNAi agent bearing at least one galactosyl-moiety. These are
useful for delivering the gene expression inhibiting activity to
cells, particularly hepatocytes, and more particularly in
therapeutic applications.
BACKGROUND OF THE INVENTION
[0003] RNA interference (RNAi) is an evolutionarily conserved,
sequence specific mechanism triggered by double stranded RNA
(dsRNA) that induces degradation of complementary target single
stranded mRNA and "silencing" of the corresponding translated
sequences (McManus and Sharp, Nature Rev. Genet. 2002, 3:737; Mello
and Donte, Nature 2004, 431:338; Meister and Tuschl, Nature 2004,
431:343; Sen and Blau, FASEB J. 2006, 20:1293).
[0004] Exploiting this mechanism has yielded a powerful tool to
unravel the function and significance of hitherto unknown or
uncharacterized genes in in vitro experiments (Hannon and Rossi,
Nature 2004, 431:371; Westbrook et al., Cold Spring Harb Symp Quant
Biol. 2005, 70:435): RNAi can be used to down-regulate or silence
the transcription and translation of a gene product of interest;
where said gene product is unknown or uncharacterized, the
development of a certain phenotype can be used to determine the
function and/or significance of the gene product. Great potential
is also seen in harnessing the underlying cellular mechanisms for
the therapy of human disease (Zhou et al., Curr Top Med Chem. 2006,
6:901): where said gene product is in any way associated with a
disease or disorder by way of its overabundance, its
down-regulation may be used in the prevention and/or therapy of the
disease or disorder.
[0005] The triggering of RNAi by dsRNA requires the dsRNA to be
localized in the cytoplasm and/or nucleus of the cell in which the
target gene is to be silenced. To this end, the dsRNA may be
introduced directly into the cell, e.g. by bringing the cells into
contact with the dsRNA, whereupon the dsRNA is actively or
passively internalized. Therein, the dsRNA may be large, e.g.
comprising 100, 200, 400 or more base pairs. A large dsRNA will be
processed in mammals by an RNAse III-like enzyme commonly called
Dicer to smaller fragments of 21 to 23 base pairs. Alternatively,
the dsRNA may be small, e.g. of the size of the Dicer products
(dsRNAs of this size, e.g. having not more than 30 base pairs, are
in the art often referred to as short interfering RNAs, or siRNAs).
The small dsRNAs, be they a product of Dicer activity or directly
introduced, are subsequently unwound by, and one strand of the
small dsRNA is incorporated into, a protein complex termed RISC
(RNA induced silencing complex). RISC then proceeds to cleave mRNAs
having a sequence complementary to the RNA strand that was
incorporated into RISC (Meister and Tuschl, Nature 2004,
431:343).
[0006] In order to harness RNAi for any purpose in vitro and/or in
vivo, a nucleic acid molecule must somehow be introduced into a
cell, preferably into a cell that forms part of a living organism,
such as a mammal or a human. If RNA interference is to live up to
its potential, the process of introducing the nucleic acid molecule
should disrupt the natural functions of the cell as little as
possible, particularly where the cell is part of a living organism.
This problem is shared by, for example, many procedures in genetic
engineering, as well as gene therapy. Numerous solutions have been
proposed, none of which is so far fully satisfactory.
[0007] The liver is one particularly attractive target for
therapeutic intervention for a number of reasons: a) it plays a
central role in many vital functions of the human body, b) it is
the first pass organ for many substances absorbed from the gut and
receives a large part of cardiac output, c) it is involved in many
diseases and unwanted conditions with high prevalence in humans,
e.g. Alagille syndrome, alcoholic liver disease,
alpha-1-antitrypsin deficiency, Budd-Chiari syndrome, biliary
atresia, Byler disease, dyslipidemias, Caroli-disease,
Crigler-Najjar Syndrome, Dubin-Johnson Syndrome, fatty liver,
galactosemia, Gilbert syndrome, glycogen storage disease I,
hemangioma, hemochromatosis, hepatitis of viral or autoimmune
etiology, liver cancer, liver fibrosis and cirrhosis, porphyria
cutanea tarda, erythrohepatic protoporphyria, Rotor syndrome,
sclerosing cholangitis, or Wilson disease.
[0008] In the development of a treatment of hepatic diseases and
conditions, it would be advantageous to have the capability to
specifically target the cells of the liver with a therapeutic
agent, e.g. an RNAi agent.
[0009] One approach documented in the literature has been
conjugating the nucleic acid to a cholesterol moiety (Soutschek,
J., et al., Nature 2004, 432:173-178), wherein the target gene was
ApoB. However, the nucleic acid showed inhibition of ApoB not
exclusively in the liver, but also in the gut of experimental
animals. For an antisense oligodesoxynucleotide (ODN), adding a
second cholesteryl moiety was effective in directing uptake of up
to nearly 90% of a certain dose of the ODN to the liver
(Bijsterbosch, M. K., et al., J. Pharmacol. Exp. Ther. 2002;
302:619).
[0010] Alternatively, a number of authors have proposed conjugating
various molecular species, including ODN, to ligand moieties, e.g.
via a variety of linkers, which bind the asialolycoprotein
receptor, to enhance hepatic uptake (Wu, G. Y., Wu, C. H., J. Biol.
Chem. 1988, 263:14621; Biessen, E.A., et al., J. Med. Chem. 1995,
38:1538; Biessen, E. A . L., et al., Biochem. J. 1999, 340:783;
Joziasse, D. H., et al., Eur. J. Biochem. 2000, 267:6501; Rump, E.
T., et al., Biochem. Pharmacol. 2000; 59:1407; Biessen, E. A.,
Methods Enzymol. 2000, 314:324; Rensen, P. C. N., et al., J. Biol.
Chem. 2001, 276:37577; Rossenberg, S. M. W., et al., J. Biol. Chem.
2002, 277:45803). The asialoglycoprotein receptor (ASGPR) is a
transmembrane glycoprotein (42 kDa) which mediates binding,
internalization and degradation of extracellular glycoproteins that
have exposed terminal galactose residues. The receptor is expressed
on the surface of hepatocytes, and only of hepatocytes, in a polar
manner, i.e. it is present on the sinusoidal and lateral plasma
membranes, but not on the bile canalicular membrane. The mammalian
hepatic ASGPR mediates the endocytosis and degradation of serum
proteins from which terminal sialic residues have been removed. The
exclusive localization of the ASGPR to the liver, as well as its
natural function in transporting comparatively large molecules into
the hepatocyte, make it an attractive option for a mediator of
liver cell targeting of therapeutic substances.
[0011] The available nucleic acid delivery systems are not yet
satisfactory in terms of safety and/or efficiency for their
utilization in in vitro experimental applications and/or human
diagnosis and therapy, and require further optimization.
[0012] The technical problem underlying the present invention is
the provision of improved methods and means for the delivery into
cells of nucleic acid molecules, and preferably of RNAi agents,
which are useful in vitro and in vivo, preferably for human
therapy. This problem has been solved by the provision of the
embodiments as characterized herein below and in the claims.
SUMMARY OF THE INVENTION
[0013] In one aspect, the invention provides an RNAi agent for
inhibiting the expression of a target gene in a cell, wherein the
RNAi agent consists of, or consists essentially of, at least two
mutually complementary oligoribonucleotide strands of between 15
and 30 nucleotides in length, wherein at least one of the
oligoribonucleotide strands is coupled to a ligand comprising at
least one linker group and at least one galactose moiety, and
wherein at least one oligoribonucleotide strand is complementary to
at least parts of an mRNA corresponding to the target gene. In one
embodiment, the ligand comprises at least two galactose moieties.
In another embodiment, the linker is a branched linker. In the RNAi
agents of the invention, the distance between the galactose
moieties may be at least 4 .ANG., at least 10 .ANG., at least 15
.ANG., or at least 20 .ANG.. Preferably, the RNAi agent is capable
of inhibiting the expression of the target gene. Preferably, the
cell harbors the asialoglycoprotein receptor on its surface. The
cell may be a hepatocyte.
[0014] In another aspect of the invention, a pharmaceutical
composition comprising (i) at least one RNAi agent of the claim 1,
and (ii) a pharmaceutical oligonucleotide strand is provided.
[0015] In yet another aspect of the invention, a method for the
manufacture of the RNAi agent of the invention is provided,
comprising the steps of (i) synthesizing said at least two mutually
complementary oligoribonucleotide strands of between 15 and 30
nucleotides in length, wherein at least one of the
oligoribonucleotide strands is coupled to a ligand comprising a
linker group and at least one galactose moiety, and (ii) effecting
the hybridization of said at least two mutually complementary
oligoribonucleotide strands. Preferably, such method further
encompasses the step of formulating the RNAi agent with a
pharmaceutical oligonucleotide strand.
[0016] In yet another aspect, a method to introduce an RNAi agent
into a cell is provided, comprising the steps of: (1) contacting
the cell with an RNAi agent of the invention.
[0017] In yet another aspect, a method to treat a subject is
provided, comprising the step of: administering to the subject a
pharmaceutical composition of the invention. Said subject is
preferably in need of a treatment for a disease or condition
related to unwanted expression of a target gene in the liver. Said
subject may be a vertebrate, more preferably a mammal, yet more
preferably a human.
[0018] In yet another aspect, a cell comprising an RNAi agent of
the invention is provided. Said cell may be a hepatocyte.
BRIEF DESCRIPTION OF DRAWINGS
[0019] FIG. 1 depicts the effects of siRNA administration (100 nM,
10 nM, 1 nM and 0,1 nM) on apoB 100 protein and mRNA levels using
oligofectamine in HuH7 cells. Protein content was measured by ELISA
and mRNA content was determined by b-DNA. Data are presented as
mean values with corresponding standard diviation of three assays
in triplicates normalized to the average level of unspecific
siRNAs. Statistical analysis was done by t-test, P*<0,001
compared to unspecific controls.
[0020] FIG. 2 depicts the results of siRNA delivery experiments (10
.mu.M, 5 .mu.M, 1 .mu.M siRNA) in the absence of transfection
agents in HuH7 cells. ApoB 100 protein and mRNA contents were
determined relative to the mean value of unspecific siRNAs (n=9).
Statistical analysis was done by t-test, P*<0,005 compared to
unspecific controls.
[0021] FIG. 3 depicts the in vitro silencing of apoB 100 protein
and mRNA in HuH7 cells after receptor activation with 5 mM
CaCl.sub.2 and siRNA treatment (10 .mu.M, 5 .mu.M and 1 .mu.M
siRNA) in the absence of transfection agents. Apo B 100 protein and
mRNA contents were determined relative to the mean value of
unspecific siRNAs (n=9). Error bars illustrate standard deviation
(s.d.) of the mean values. Statistical analysis was done by t-test,
P*<0.0001 compared to unspecific controls.
[0022] FIG. 4 depicts the results of competition experiments with 1
mM GalNAc on apoB 100 protein and mRNA levels after receptor
stimulation and siRNA treatment (10 .mu.M, 5 .mu.M and 1 siRNA) in
the absence of transfection agents in HuH7 cells. Apo B 100 protein
and mRNA contents were determined relative to the mean value of
unspecific siRNAs (n=6). Error bars illustrate standard deviations
of the means. Statistical analysis was done by t-test, P*<0.0001
compared to unspecific controls.
[0023] FIG. 5 depicts the results of delivery experiments with
fluorescently labeled siRNAs (10 .mu.M) in HuH7 cells after
receptor activation with 5 mM CaCl2 (right panel) or without
receptor activation (left panel) in the absence of transfection
agents. Localisation of Cy3 labeled siRNAs was determined by
fluorescence microscopy.
[0024] FIG. 6 depicts the synthesis scheme for
1--O-{4-[(2-cyanoethoxy)-N,N-diisopropylamino-phosphanyloxy]-butyl}-6-O-(-
4-methoxytriphenylmethyl)-2,3,4-tri-O-acetyl-.beta.-D-galactopyranoside.
Reagents and conditions: (a) Benzylamine, THF; (b) DBU,
CCl.sub.3CN, CH.sub.2Cl.sub.2 (71.5%); (c)
4-(tert-butyl-dimethylsilyloxy)-1-butanol, AgOTf, CH.sub.2Cl.sub.2,
-78.degree. C. (77.9%); (d) Sodiummethylate, MeOH; (e) MMT-C1,
Pyridine; (f) Acetanhydride, Pyridine (39.6%); (g)
tert-butyl-ammoniumfluoride, THF (70.2%); (h)
2-cyanoethyl-N,N,N,N-tetraisopropylphosphane, DIPEA, ETT, ACN
(74.3%).
[0025] FIG. 7 depicts the chemical structures of SBGAL and SBTEGGAL
siRNA conjugates. The SBGAL conjugate was generated by coupling a
symmetrical branching linkage (SB) during RNA solid phase synthesis
to the 5'-end of the sense strand followed by coupling of the
galactose phosphoramidite 9. The SBTEGGAL conjugate additionally
contained a tetraethylene glycol linkage (TEG) between the SB
linkage and the sugar moiety.
DETAILED DESCRIPTION OF THE INVENTION
[0026] The term "alkyl" refers to a hydrocarbon chain that may be a
straight chain or branched chain, containing the indicated number
of carbon atoms. For example, C.sub.1-C.sub.12 alkyl indicates that
the group may have from 1 to 12 (inclusive) carbon atoms in it. The
term "haloalkyl" refers to an alkyl in which one or more hydrogen
atoms are replaced by halo, and includes alkyl moieties in which
all hydrogens have been replaced by halo (e.g., perfluoroalkyl).
Alkyl and haloalkyl groups may be optionally inserted with O, N, or
S. The terms "aralkyl" refers to an alkyl moiety in which an alkyl
hydrogen atom is replaced by an aryl group. Aralkyl includes groups
in which more than one hydrogen atom has been replaced by an aryl
group. Examples of "aralkyl" include benzyl, 9-fluorenyl,
benzhydryl, and trityl groups.
[0027] The term "alkenyl" refers to a straight or branched
hydrocarbon chain containing 2-8 carbon atoms and characterized in
having one or more double bonds. Examples of a typical alkenyl
include, but not limited to, allyl, propenyl, 2-butenyl, 3-hexenyl
and 3-octenyl groups. The term "alkynyl" refers to a straight or
branched hydrocarbon chain containing 2-8 carbon atoms and
characterized in having one or more triple bonds. Some examples of
a typical alkynyl are ethynyl, 2-propynyl, and 3-methylbutynyl, and
propargyl. The sp.sup.2 and sp.sup.3 carbons may optionally serve
as the point of attachment of the alkenyl and alkynyl groups,
respectively.
[0028] The term "alkoxy" refers to an --O-alkyl radical. The term
"aminoalkyl" refers to an alkyl substituted with an amino. The term
"mercapto" refers to an --SH radical. The term "thioalkoxy" refers
to an --S-alkyl radical.
[0029] The term "alkylene" refers to a divalent alkyl (i.e.,
--R--), e.g., --CH.sub.2--, --CH.sub.2CH.sub.2--, and
--CH.sub.2CH.sub.2CH.sub.2--. The term "alkylenedioxo" refers to a
divalent species of the structure --O--R--O--, in which R
represents an alkylene.
[0030] The term "aryl" refers to an aromatic monocyclic, bicyclic,
or tricyclic hydrocarbon ring system, wherein any ring atom can be
substituted. Examples of aryl moieties include, but are not limited
to, phenyl, naphthyl, anthracenyl, and pyrenyl.
[0031] The term "cycloalkyl" as employed herein includes saturated
cyclic, bicyclic, tricyclic,or polycyclic hydrocarbon groups having
3 to 12 carbons, wherein any ring atom can be substituted. The
cycloalkyl groups herein described may also contain fused rings.
Fused rings are rings that share a common bond. Examples of
cycloalkyl moieties include, but are not limited to, cyclohexyl,
adamantyl, norbornyl, and decalin.
[0032] The term "heterocyclyl" refers to a nonaromatic 3-10
membered monocyclic, 8-12 membered bicyclic, or 11-14 membered
tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6
heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said
heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3,
1-6, or 1-9 heteroatoms of N, O, or S if monocyclic, bicyclic, or
tricyclic, respectively), wherein any ring atom capable of
substitution can be substituted by a substituent. The heterocyclyl
groups herein described may also contain fused rings. Fused rings
are rings that share a common bond. Examples of heterocyclyl
include, but are not limited to tetrahydrofuranyl,
tetrahydropyranyl, piperidinyl, morpholino, pyrrolinyl and
pyrrolidinyl.
[0033] The term "heteroaryl" refers to an aromatic 5-8 membered
monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic
ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms
if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms
selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9
heteroatoms of N, O, or S if monocyclic, bicyclic, or tricyclic,
respectively), wherein any ring atom can be substituted.
[0034] The term "oxo" refers to an oxygen atom, which forms a
carbonyl when attached to carbon, an N-oxide when attached to
nitrogen, and a sulfoxide or sulfone when attached to sulfur.
[0035] The term "acyl" refers to an alkylcarbonyl,
cycloalkylcarbonyl, arylcarbonyl, heterocyclylcarbonyl, or
heteroarylcarbonyl substituent, any of which may be further
substituted by substituents.
[0036] The term "substituents" refers to a group "substituted" on
an alkyl, cycloalkyl, alkenyl, alkynyl, heterocyclyl,
heterocycloalkenyl, cycloalkenyl, aryl, or heteroaryl group at any
atom of that group. Suitable substituents include, without
limitation, alkyl, alkenyl, alkynyl, alkoxy, halo, hydroxy, cyano,
nitro, amino, SO.sub.3H, sulfate, phosphate, perfluoroalkyl,
perfluoroalkoxy, methylenedioxy, ethylenedioxy, carboxyl, oxo,
thioxo, imino (alkyl, aryl, aralkyl), S(O).sub.nalkyl (where n is
0-2), S(O).sub.n aryl (where n is 0-2), S(O).sub.n heteroaryl
(where n is 0-2), S(O).sub.n heterocyclyl (where n is 0-2), amine
(mono-, di-, alkyl, cycloalkyl, aralkyl, heteroaralkyl, and
combinations thereof), ester (alkyl, aralkyl, heteroaralkyl), amide
(mono-, di-, alkyl, aralkyl, heteroaralkyl, and combinations
thereof), sulfonamide (mono-, di-, alkyl, aralkyl, heteroaralkyl,
and combinations thereof), unsubstituted aryl, unsubstituted
heteroaryl, unsubstituted heterocyclyl, and unsubstituted
cycloalkyl. In one aspect, the substituents on a group are
independently any one single, or any subset of the aforementioned
substituents.
[0037] An "RNAi agent", as used herein, means a molecule (a
"molecule", as used herein, is the smallest unit of a substance
that has all the properties of that substance; "molecule",
therefore, does not necessarily imply, nor exclude, that all the
atoms from which it is formed are linked by covalent bonds)
consisting of, consisting essentially of, or comprising, at least
two mutually complementary oligoribonucleotide strands of between
15 and 30 nucleotides in length, wherein at least one of the
oligoribonucleotide strands is coupled to a ligand comprising at
least one linker group and at least one galactose moiety, and
wherein at least one oligoribonucleotide strand is complementary to
at least parts of an mRNA corresponding to the target gene. The
strand that is complementary to the target gene mRNA is herein
referred to as the "antisense strand", the respective other strand
as the "sense strand". By virtue of their mutual complementarity,
the two strands are capable of hybridization, forming a duplex
structure with between 15 and 30, and preferably 15, 16, 17, 18,
19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29 or 30 nucleotide pairs.
The RNA strands may have the same or a different number of
nucleotides, and each strand may individually and independently be
15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29 or 30
nucleotides in length. Ranges between any two of these numbers are
also contemplated, both for the number of base pairs as well as for
the length of the individual strands. The maximum number of base
pairs is the number of nucleotides in the shortest strand.
[0038] The two strands may be complementary such that all of the
nucleotides in both strands are involved in nucleotide pairs, or
they may form single-stranded regions, such as one or more of
overhangs, bulges, loops, etc. Overhangs, if present, are
preferably of a length of 1-4, and more preferably 2 or 3
nucleotides in length. In one embodiment, the length of the
overhang(s) does not exceed 100, or 50, or 20, or 10, or 5
nucleotides. They may be located at the 3'- or the 5'-end of either
strand, but preferred embodiments comprise at least one overhang on
the 3'-ends of the antisense strand, or of both strands.
[0039] The two strands forming the duplex structure may be
different portions of one larger RNA molecule, or they may be
separate RNA molecules. Where the two strands are part of one
larger molecule, and therefore are connected by an uninterrupted
chain of nucleotides between the 3'-end of one strand and the
5'-end of the respective other strand forming the duplex structure,
the connecting RNA chain is referred to as a "hairpin loop". Where
the two strands are connected covalently by means other than an
uninterrupted chain of nucleotides between the 3'-end of one strand
and the 5'-end of the respective other strand forming the duplex
structure, the connecting structure is referred to as a "strand
linkage". Where the two strands are connected by a hairpin loop,
and the duplex structure consists of not more than 30 nucleotide
pairs, the RNAi agent may be referred to herein as a short hairpin
RNA (shRNA). Where the two strands are not connected, or connected
by a strand linkage, and the duplex structure consists of not more
than 30 nucleotide pairs, the RNAi agent may be referred to herein
as a short interfering RNA (siRNA).
[0040] As used herein, and unless otherwise indicated, the term
"complementary," when used to describe a first nucleotide sequence
in relation to a second nucleotide sequence, refers to the ability
of an oligonucleotide or polynucleotide comprising the first
nucleotide sequence to hybridize and form a duplex structure under
certain conditions with an oligonucleotide or polynucleotide
comprising the second nucleotide sequence, as will be understood by
the skilled person. Such conditions can, for example, be stringent
conditions, where stringent conditions may include: 400 mM NaCl, 40
mM PIPES pH 6.4, 1 mM EDTA, 50.degree. C. or 70.degree. C. for
12-16 hours followed by washing. "Complementary" sequences may be
fully complementary, or they may include mismatches, as long as
they are still able to hybridize under the chosen conditions. For
purposes of the present invention, an overhang shall not be
considered a mismatch. Preferably, complementary sequences will
include not more than 1, not more than 2, not more than 3, not more
than 4, or not more than 5 mismatches, if any. The degree of
complementarity will, at any rate, be such that stable and specific
binding occurs between the two oligonucleotides comprising the
sequences referred to as complementary. Specific binding requires a
sufficient lack of complementarity to non-target sequences under
conditions in which specific binding is desired, i.e., under
physiological conditions in the case of in vivo assays or
therapeutic treatment, or in the case of in vitro assays, under
conditions in which the assays are performed. It has been shown
that a single mismatch between targeted and non-targeted sequences
can be sufficient to provide discrimination for siRNA targeting of
an mRNA (Brummelkamp et al., Cancer Cell, 2002, 2:243).
[0041] In one embodiment, an RNAi agent's antisense strand is
"sufficiently complementary" to a target RNA, such that the RNAi
agent inhibits production of protein encoded by the target mRNA.
The target RNA can be, e.g., a pre-mRNA or mRNA endogenous to a
subject or organism. In another embodiment, the RNAi agent is
"fully complementary" to a target RNA, e.g., the target RNA and the
RNAi agent can anneal to form a hybrid made exclusively of
Watson-Crick base pairs in the region of exact complementarity. A
"sufficiently complementary" RNAi agent antisense strand can
include a region (e.g., of at least 7 nucleotides) that is exactly
complementary to the target RNA. Moreover, in some embodiments, the
RNAi agent specifically discriminates a single-nucleotide
difference. In this case, the RNAi agent only down-regulates gene
expression from an mRNA if exact complementarity is found in the
region of the single-nucleotide difference.
[0042] "RNA", "oligoribonucleotide" and "oligoribonucleotide
strand", as used herein, shall refer to nucleic acids having
predominantly RNA-like properties, e.g. having the ability to
hybridize to a substantially complementary RNA, forming an A-type
helix. Generally, an RNA, oligoribonucleotide or
oligoribonucleotide strand will consist mostly, or exclusively, of
ribonucleotides, i.e. cytidine, adenosine, guanosine and uridine
nucleosides interconnected by 5'-3'-monophosphate bridging groups.
However, one or more, or all, nucleotides may be 2'-O-methyl
ribonucleotides, or nucleotides not naturally occurring in RNA, for
example, without limitation, deoxyribonucleotides, inosines,
2'-deoxy-2'-fluoro-, or 2'-O-[(CH.sub.2).sub.nO].sub.mCH.sub.3
ribonucleotides, as long as the overall molecule retains
predominantly RNA-like properties. In addition, or alternatively,
the RNA may comprise modified internucleoside linkages, e.g.
phosphorothioates, phosphorodithioates, phosphotriesters,
aminoalkylphosphotriesters, methyl and other alkyl phosphonates
including 3'-alkylene phosphonates and chiral phosphonates,
phosphinates, phosphoramidates including 3'-amino phosphoramidate
and aminoalkylphosphoramidates, thionophosphoramidates,
thionoalkylphosphonates, thionoalkylphosphotriesters, and
boranophosphates having normal 3'-5' linkages, 2'-5' linked analogs
of these, and those having inverted polarity wherein the adjacent
pairs of nucleoside units are linked 3'-5' to 5'-3' or 2'-5' to
5'-2'. Various salts, mixed salts and free acid forms are also
included. Further nucleotide modifications are well known to the
skilled person and are encompassed by the present invention, e.g.
those described in WO 03/070918 and U.S. Pat. Nos. 3,687,808;
4,469,863; 4,476,301; 4,845,205; 4,981,957; 5,023,243; 5,034,506;
5,118,800; 5,134,066; 5,166,315; 5,175,273; 5,177,195; 5,185,444;
5,188,897; 5,214,134; 5,216,141; 5,235,033; 5,264,423; 5,264,564;
5,276,019; 5,278,302; 5,286,717; 5,319,080; 5,321,131; 5,359,044;
5,367,066; 5,393,878; 5,399,676; 5,405,938; 5,405,939; 5,432,272;
5,434,257; 5,446,137; 5,453,496; 5,455,233; 5,457,187; 5,459,255;
5,466,677; 5,466,677; 5,466,786; 5,470,967; 5,476,925; 5,484,908;
5,489,677; 5,502,177; 5,514,785; 5,519,126; 5,519,134; 5,525,711;
5,536,821; 5,541,307; 5,541,316; 5,550,111; 5,552,540; 5,561,225;
5,563,253; 5,567,811; 5,571,799; 5,576,427; 5,587,361; 5,587,469;
5,591,722; 5,594,121; 5,596,086; 5,596,091; 5,597,909; 5,602,240;
5,608,046; 5,610,289; 5,610,300; 5,614,617; 5,618,704; 5,623,070;
5,625,050; 5,627,053; 5,633,360; 5,639,873; 5,646,265; 5,658,873;
5,663,312; 5,670,633; 5,677,437; 5,677,439; 5,681,941; 5,700,920;
5,750,692, all of which are hereby incorporated herein by
reference. Further embodiments are described below.
[0043] The introduction or transfer process of nucleic acid
molecules of interest into a cell is by itself well known.
"Introduction or transfer" means that the nucleic acid is, at the
outset of the transfer process, located outside the cell or on the
outer surface of the cell's membrane, and, at the end of the
process, located inside said cell, or within its membrane, or on
the inner surface of the membrane. The "introduction or transfer"
of a nucleic acid molecule into a cell is also referred to as
"transfection". Transfection can be verified by any appropriate
method, for example by measuring a biological, chemical or physical
effect associated with its presence inside the cell. In the case of
RNAi agents, the effect to be measured may, for example, be the
inhibition of the expression of the target gene of the RNAi
agent.
[0044] At least one strand of the RNAi agents of the invention is
coupled to a ligand comprising at least one linker group and at
least one galactose moiety. "Coupled to a ligand", as used herein,
means that the ligand is associated with the RNA strand in a manner
that substantially prevents the separation of the ligand from the
RNA strand under the conditions most relevant to the use of the
RNAi agent, e.g., in blood or serum at 37.degree. C. for
therapeutics, or in cell growth media for RNAi agents for in vitro
use. "Substantially prevents the separation of the ligand from the
RNA strand" means that in the majority of the RNAi agent molecules,
e.g. in more than 80%, more than 90%, more than 95%, more than 99%,
or preferably more than 99.9% of RNAi agent molecules, the ligand
remains associated with the RNA strand under the said conditions.
Preferably, but not necessarily, the ligand is coupled to the RNA
strand by means of a covalent bond. Alternatively, the coupling of
the ligand to the RNA strand may be effected by, for example, van
der Waals forces, hydrogen bonds, ionic interactions, or any other
molecular interaction strong enough under the said conditions to
substantially prevent the separation of the ligand from the RNA
strand under the said conditions.
[0045] The ligand can be placed at an end of the RNA strand,
preferably at the 3'-end. The ligand can also be placed at the
5'end, or within the middle of the RNA strand. In some embodiments,
more than one ligand can be coupled to the RNA strand, or to both
strands of the RNAi agent. For example, a ligand can be coupled to
the 3' end of one RNA strand, e.g. the sense or antisense strand; a
ligand can be coupled to an end, e.g., a 3' end, and to the middle
of an RNA strand, e.g. the sense or antisense strand; a ligand can
be coupled to the 3' end and the 5' of an RNA strand, e.g. the
sense or antisense strand; a ligand can be coupled to the 3' end,
the 5' end, and to one or more internal positions of an RNA strand,
e.g. the sense or antisense strand; a ligand can be coupled to the
3'-end of both the sense and the antisense strands; a ligand can be
coupled to the 5'-end of both the sense and the antisense strands;
a ligand can be coupled to the 3'-end of the sense and the 5'-end
of the sense strand, or vice versa; a ligand can be coupled to the
3'-end of both the sense and the antisense strands, and to an
internal position on either strand, e.g. the sense and the
antisense strand; the skilled person will readily envision further
permutations of this scheme, which are all envisaged by the present
invention.
[0046] The Galactose Moiety
[0047] The galactose moiety is a galactopyranosyl or, preferably, a
N-acetyl galactosaminpyranosyl group of general formula
C.sub.6(OR.sup.1)(OR.sup.2)(OR.sup.3)(OR.sup.4)(OR.sup.6)O or
C.sub.6(OR.sup.1)(NHCH.sub.2COOH)(OR.sup.3)(OR.sup.4)(OR.sup.6)O,
wherein (OR.sup.1) is attached to the C1 position of the
galactopyranose ring, (OR.sup.2) or (NHCH.sub.2COOH) is attached to
the C2 position of the galactopyranose ring, (OR.sup.3) is attached
to the C3 position of the galactopyranose ring, and so forth, and
wherein each of (OR.sup.1)--(OR.sup.4) and (OR.sup.6) are
independently OH, lower alkyloxy or acyloxy (C.sub.1-C.sub.6), or
replaced by one of the linker groups described below, but wherein
at least one of (OR.sup.1)--(OR.sup.4) and (OR.sup.6) is replaced
by one of the linker groups described below. Preferably, R.sup.2
(where present), R.sup.3, R.sup.4, and R.sup.6 are H, and
(OR.sup.1) is replaced by one of the linker groups described below.
Preferably, the pyranose ring is in the .beta.-anomeric
conformation.
[0048] The presence of more than one, e.g., 2, 3, or 4 or more,
galactose moieties markedly increases the affinity of a ligand for
the asialoglycoprotein receptor, leading to increased transfection
efficiency of the RNAi agent comprising such more than one
galactose moities.
[0049] Linker Groups
[0050] The conjugation or coupling of the ligand to the RNA strand
is mediated by the linker group, where only one linker group is
present, or by one or more of the linker groups, if more than one
linker group is present. The intended nature of the conjugation or
coupling interaction will determine the choice of linker group.
[0051] In certain embodiments, a galactose moiety is coupled to an
oligonucleotide strand via the intermediacy of an intervening
linker group. Linker groups are connected to the oligonucleotide
strand at a linker group attachment point (LAP) and may include any
C.sub.1C.sub.100 carbon-containing moiety, (e.g. C.sub.1-C.sub.75,
C.sub.1-C.sub.50, C.sub.1-C20, C.sub.1-C.sub.10; C.sub.1, C.sub.2,
C.sub.3, C.sub.4, C.sub.5, C.sub.6, C.sub.7, C.sub.8, C.sub.9, or
C.sub.10), preferably having at least one oxygen atom, at least one
phosphorous atom, and/or at least one nitrogen atom. In preferred
embodiments, the phosphorous atom forms part of a terminal
phosphate, or phosphorothioate, group on the linker group, which
may serve as a connection point for the oligonuclotide strand. In
preferred embodiments, the nitrogen atom forms part of a terminal
ether, ester, amino or amido (NHC(O)--) group on the linker group,
which may serve as a connection point for the galactose moiety.
Preferred linker groups (underlined) include
LAP-X--(CH.sub.2).sub.nNH--; LAP-X--C(O)(CH.sub.2).sub.nNH--;
LAP-X--NR''''(CH.sub.2).sub.n,NH--,
LAP-X--C(O)--(CH.sub.2).sub.n--C(O)--;
LAP-X--C(O)--(CH.sub.2).sub.n--C(O)O--; LAP-X--C(O)--O--;
LAP-X--C(O)--(CH.sub.2).sub.n,--NH --C(O)--;
LAP-X--C(O)--(CH.sub.2).sub.n--; LAP-X--C(O)--NH--; LAP-X--C(O)--;
LAP-X--(CH.sub.2).sub.n--C(O)--; LAP-X--(CH.sub.2).sub.n--C(O)O--;
LAP-X--(CH.sub.2).sub.n--; or LAP-X--(CH.sub.2).sub.n--NH --C(O)--;
in which --X is (--O--(R''''O)P(O)--O).sub.m,
(--O--(R''''O)P(S)--O--).sub.m, (--O--(R''''S)P(O)--O).sub.m,
(--O--(R''''S)P(S)--O).sub.m, (--O--(R''''O)P(O)--S).sub.m,
(--S--(R''''O)P(O)--O).sub.m, or nothing, n is 1-20 (e.g., 1, 2, 3,
4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20), m
is 1 to 3, and R'''' is H or C.sub.1-C.sub.6 alkyl. Preferably, n
is 5, 6, or 11. In other embodiments, the nitrogen may form part of
a terminal oxyamino group, e.g., --ONH.sub.2, or hydrazino group,
--NHNH.sub.2. The linker group may optionally be substituted, e.g.,
with hydroxy, alkoxy, perhaloalkyl, and/or optionally inserted with
one or more additional heteroatoms, e.g., N, O, or S. Preferred
linker groups may include, e.g., LAP-X--(CH.sub.2).sub.nNH--;
LAP-X--C(O)(CH.sub.2).sub.nNH--; LAP-X-NR''''(CH.sub.2).sub.nNH--;
LAP-X--(CH.sub.2).sub.nONH--; LAP-X--C(O)(CH.sub.2).sub.nONH--;
LAP-X--NR''''(CH.sub.2).sub.nONH--;
LAP-X--(CH.sub.2).sub.nNHNH.sub.2--,
LAP-X--C(O)(CH.sub.2).sub.nNHNH.sub.2--;
LAP-X--NR''''(CH.sub.2).sub.nNHNH.sub.2--;
LAP-X--C(O)--(CH.sub.2).sub.n--C(O)--;
LAP-X--C(O)--(CH.sub.2).sub.nC(O)O--; LAP-X--C(O)--O--;
LAP-X--C(O)--(CH.sub.2).sub.n--NH --C(O)--;
LAP-X--C(O)--(CH.sub.2).sub.n--; LAP-X--C(O)--NH--; LAP-X--C(O)--;
LAP-X--(CH.sub.2).sub.n--C(O)--; LAP-X--(CH.sub.2).sub.n--C(O)O--;
LAP-X--(CH.sub.2).sub.n--; or LAP-X--(CH.sub.2).sub.n--NH--C(O)--.
In some embodiments, amino terminated linker groups (e.g.,
NH.sub.2, ONH.sub.2, NH.sub.2NH.sub.2) can form an imino bond
(i.e., C.dbd.N) with the ligand. In some embodiments, amino
terminated linker groups (e.g., NH.sub.2, ONH.sub.2,
NH.sub.2NH.sub.2) can be acylated, e.g., with C(O)CF.sub.3.
[0052] In some embodiments, the linker group can terminate with a
mercapto group (i.e., SH) or an olefin (e.g., CH.dbd.CH.sub.2). For
example, the linker group can be LAP-X--(CH.sub.2).sub.n--SH,
LAP-X--C(O)(CH.sub.2).sub.nSH, LAP-X--(CH.sub.2).sub.n
--(CH.dbd.CH.sub.2), or
LAP-X--C(O)(CH.sub.2).sub.n(CH.dbd.CH.sub.2), in which X and n can
be as described for the linker groups above. In certain
embodiments, the olefin can be a Diels-Alder diene or dienophile.
The linker group may optionally be substituted, e.g., with hydroxy,
alkoxy, perhaloalkyl, and/or optionally inserted with one or more
additional heteroatoms, e.g., N, O, or S. The double bond can be
cis or trans or E or Z.
[0053] In other embodiments the linker group may include an
electrophilic moiety, preferably at the terminal position of the
linker group. Preferred electrophilic moieties include, e.g., an
aldehyde, alkyl halide, mesylate, tosylate, nosylate, or brosylate,
or an activated carboxylic acid ester, e.g. an NHS ester, or a
pentafluorophenyl ester. Preferred linker groups (underlined)
include LAP-X--(CH.sub.n).sub.nCHO; LAP-X--C(O)(CH.sub.2).sub.nCHO;
or LAP-X--NR''''(CH.sub.2)CHO, in which n is 1-6 and R'''' is
C.sub.1-C.sub.6 alkyl; or LAP-X--(CH.sub.2).sub.nC(O)ONHS;
LAP-X--C(O)(CH.sub.2).sub.nC(O)ONHS; or
LAP-X--NR''''(CH.sub.2).sub.nC(O)ONHS, in which n is 1-6 and R''''
is C.sub.1-C.sub.6 alkyl;
LAP-X--(CH.sub.2).sub.nC(O)OC.sub.6F.sub.5;
LAP-X--C(O)(CH.sub.2).sub.nC(O)OC.sub.6F.sub.5; or
LAP-X--NR''''(CH.sub.2).sub.nC(O)OC.sub.6F.sub.5, in which n is
1-11 and R'''' is C.sub.1-C.sub.6 alkyl; or
--(CH.sub.2).sub.nCH.sub.2LG;
LAP-X--C(O)(CH.sub.2).sub.nCH.sub.2LG; or
LAP-X--NR''''(CH.sub.2).sub.nCH.sub.2LG, in which X, R'''' and n
can be as described for the linker groups above (LG can be a
leaving group, e.g., halide, mesylate, tosylate, nosylate,
brosylate). Coupling the oligonucleotide-linker group to the
galactose moiety can be carried out by coupling a nucleophilic
group of the galactose moiety with an electrophilic group on the
linker group.
[0054] In other embodiments, other protected amino groups can be at
the terminal position of the linker group, e.g., alloc, monomethoxy
trityl (MMT), trifluoroacetyl, Fmoc, or aryl sulfonyl (e.g., the
aryl portion can be ortho-nitrophenyl or ortho,
para-dinitrophenyl).
[0055] In any of the above linker groups, in addition, one, more
than one, or all, of the n-CH.sub.2--groups may be replaced by one
or a combination of, e.g., X, as defined above,
--Y--(CH.sub.2).sub.m--, --Y--(C(CH.sub.3)H).sub.m--,
--Y--C((CH.sub.2).sub.pCH.sub.3)H).sub.m--,
--Y--(CH.sub.2--C(CH.sub.3)H).sub.m,
--Y--(CH.sub.2--C((CH.sub.2).sub.pCH.sub.3)H).sub.m--,
--CH.dbd.CH--, or --C.ident.C--, wherein Y is O, S, Se, S--S, S(O),
S(O).sub.2, m is 1-4 and p is 0-4.
[0056] Where more than one galactose moiety is present on the same
ligand, the more than one galactose moieties may be linked to the
oligonucleotide strand in a linear fashion, or, preferably, by a
branched linker group. When connected in linear fashion, the
galactose moieties may be attached to the linker group as side
groups (i.e., every galactose moiety is attached to a linker group
only at one point), and/or one or more of the galactose moieties
may be interjected between linker groups (i.e., one or more
galactose moieties are attached to linker groups at two points,
e.g. via the C1 and the C6 positions).
[0057] Preferably, the linker group is a branched linker group, and
more preferably a symmetric branched linker group. The branch point
will be an at least trivalent, but may be a tetravalent,
pentavalent, or hexavalent atom, or a group presenting such
multiple valencies. In preferred embodiments, the branch point is a
glycerol, or glycerol triphosphate, group. Preferred embodiments of
branched linker groups are, for example, without limitation, those
shown in FIG. 7.
[0058] In embodiments comprising more than one galactose moieties,
the linker group(s) preferably provide for a certain distance
between the galactose moieties, e.g. more than 5 .ANG., preferably
more than 10 .ANG., more preferably more than 15 .ANG., or most
preferably more than 20 .ANG.. The distance between the galactose
moieties may influence their ability to bind to and crosslink to
more than one asialoglycoprotein receptor on the cell's
surface.
[0059] RNA Strands
[0060] An RNAi agent of the invention includes a region of
sufficient complementarity to the target gene, and is of sufficient
length in terms of nucleotides, such that antisense strand may form
a duplex with the target nucleic acid. The RNAi agent can modulate
the function of the targeted molecule. For example, when the
targeted molecule is an mRNA or pre-mRNA, the RNAi agent can
inhibit gene expression; when the target is a microRNA (miRNA), the
RNAi agent will inhibit the miRNA function and will thus
up-regulate expression of the mRNAs targeted by the particular
miRNA; when the target is a region of a pre-mRNA the affects
splicing, the RNAi agent can alter the choice of splice site and
thus the mRNA sequence; when the RNAi agent functions as an miRNA,
expression of the targeted mRNA is inhibited.
[0061] A RNAi agent is, or includes, a region that is at least
partially, and in some embodiments fully, complementary to the
target RNA. It is not necessary that there be perfect
complementarity between the RNAi agent and the target, but the
correspondence must be sufficient to enable the RNAi agent, or a
cleavage product thereof, to modulate (e.g., inhibit) target gene
expression.
[0062] An RNAi agent will preferably have one or more of the
following properties:
[0063] (1) it will be of the Formula 1, 2, 3, or 4 described
below;
[0064] (2) it will have a 5' modification that includes one or more
phosphate groups or one or more analogs of a phosphate group;
[0065] (3) it will, despite modifications, even to a very large
number of bases specifically base pair and form a duplex structure
with a homologous target RNA of sufficient thermodynamic stability
to allow modulation of the activity of the targeted RNA;
[0066] (4) it will, despite modifications, even to a very large
number, or all of the nucleosides, still have "RNA-like"
properties, i.e., it will possess the overall structural, chemical
and physical properties of an RNA molecule, even though not
exclusively, or even partly, of ribonucleotide-based content. For
example, all of the nucleotide sugars can contain e.g., 2'OMe, 2'
fluoro in place of 2' hydroxyl. Such agent can still be expected to
exhibit RNA-like properties. While not wishing to be bound by
theory, the electronegative fluorine prefers an axial orientation
when attached to the C2' position of ribose. This spatial
preference of fluorine can, in turn, force the sugars to adopt a
C.sub.3'-endo pucker. This is the same puckering mode as observed
in RNA molecules and gives rise to the RNA-characteristic
A-family-type helix. Further, since fluorine is a good hydrogen
bond acceptor, it can participate in the same hydrogen bonding
interactions with water molecules that are known to stabilize RNA
structures. (Generally, it is preferred that a modified moiety at
the 2' sugar position will be able to enter into hydrogen-bonding
which is more characteristic of the 2'-OH moiety of a
ribonucleotide than the 2'-H moiety of a deoxyribonucleotide. A
preferred RNAi agent will: exhibit a C.sub.3'-endo pucker in all,
or at least 50, 75,80, 85, 90, or 95% of its sugars; exhibit a
C.sub.3'-endo pucker in a sufficient amount of its sugars that it
can give rise to a the RNA-characteristic A-family-type helix; will
have no more than 20, 10, 5, 4, 3, 2, or 1 sugar which is not a
C.sub.3'-endo pucker structure.
[0067] Preferred 2'-modifications with C3'-endo sugar pucker
include:
[0068] 2'-OH, 2'-O-Me, 2'-O-methoxyethyl, 2'-O-aminopropyl, 2'-F,
2'-O --CH.sub.2--CO--NHMe,
2'-O--CH.sub.2--CH.sub.2--O--CH.sub.2--CH.sub.2--N(Me).sub.2,
LNA
[0069] (5) regardless of the nature of the modification, and even
though the RNAi agent can contain deoxynucleotides or modified
deoxynucleotides, it is preferred that DNA molecules, or any
molecule in which more than 50, 60, or 70% of the nucleotides in
the molecule are deoxyribonucleotides, or modified
deoxyribonucleotides which are deoxy at the 2' position, are
excluded from the definition of RNAi agent.
[0070] Preferred 2'-modifications with a C2'-endo sugar pucker
include:
[0071] 2'-H, 2'-Me, 2'-S-Me, 2'-Ethynyl, 2'-ara-F.
[0072] Sugar modifications can also include L-sugars and
2'-5'-linked sugars.
[0073] RNAi agents discussed herein include otherwise unmodified
nucleotides as well as nucleotides that have been modified, e.g.,
to improve efficacy, and polymers of nucleoside surrogates.
Unmodified RNA refers to a molecule in which the components of the
nucleic acid, namely sugars, bases, and phosphate moieties, are the
same or essentially the same as that which occur in nature,
preferably as occur naturally in the human body. The art has
referred to rare or unusual, but naturally occurring, RNAs as
modified RNAs, see, e.g., Limbach et al. (Nucleic Acids Res., 1994,
22:2183-2196). Such rare or unusual RNAs, often termed modified
RNAs, are typically the result of a post transcriptional
modification and are within the term unmodified RNA as used herein.
Modified RNA, as used herein, refers to a molecule in which one or
more of the components of the nucleic acid, namely sugars, bases,
and phosphate moieties, are different from that which occur in
nature, preferably different from that which occurs in the human
body. While they are referred to as "modified RNAs" they will of
course, because of the modification, include molecules that are
not, strictly speaking, RNAs. Nucleoside surrogates are molecules
in which the ribophosphate backbone is replaced with a
non-ribophosphate construct that allows the bases to the presented
in the correct spatial relationship such that hybridization is
substantially similar to what is seen with a ribophosphate
backbone, e.g., non-charged mimics of the ribophosphate backbone.
Examples of all of the above are discussed herein.
[0074] As nucleic acids are polymers of subunits or monomers, many
of the modifications described below occur at a position which is
repeated within a nucleic acid, e.g., a modification of a base, or
a phosphate moiety, or a non-linking O of a phosphate moiety. In
some cases the modification will occur at all of the subject
positions in the nucleic acid but in many, and infact in most cases
it will not. By way of example, a modification may only occur at a
3' or 5' terminal position, may only occur in a terminal regions,
e.g. at a position on a terminal nucleotide or in the last 2, 3, 4,
5, or 10 nucleotides of a strand. The ligand can be at attached at
the 3' end, the 5' end, or at an internal position, or at a
combination of these positions. For example, the ligand can be at
the 3' end and the 5' end; at the 3' end and at one or more
internal positions; at the 5' end and at one or more internal
positions; or at the 3' end, the 5' end, and at one or more
internal positions. E.g., a phosphorothioate modification at a
non-linking O position may only occur at one or both termini, or
may only occur in a terminal region, e.g., at a position on a
terminal nucleotide or in the last 2, 3, 4, 5, or 10 nucleotides of
the oligonucleotide. The 5' end can be phosphorylated.
[0075] Modifications and nucleotide surrogates are discussed
below.
##STR00001##
[0076] The scaffold presented above in Formula 1 represents a
portion of a ribonucleic acid. The basic components are the ribose
sugar, the base, the terminal phosphates, and phosphate
internucleotide linkers. Where the bases are naturally occurring
bases, e.g., adenine, uracil, guanine or cytosine, the sugars are
the unmodified 2' hydroxyl ribose sugar (as depicted) and W, X, Y,
and Z are all O, Formula 1 represents a naturally occurring
unmodified oligoribonucleotide.
[0077] Unmodified oligoribonucleotides may be less than optimal in
some applications, e.g., unmodified oligoribonucleotides can be
prone to degradation by e.g., cellular nucleases. Nucleases can
hydrolyze nucleic acid phosphodiester bonds. However, chemical
modifications to one or more of the above RNA components can confer
improved properties, and, e.g., can render oligoribonucleotides
more stable to nucleases. Unmodified oligoribonucleotides may also
be less than optimal in terms of offering linker group points for
attaching ligands or other moieties to an RNAi agent.
[0078] Modified nucleic acids and nucleotide surrogates can include
one or more of:
[0079] (i) alteration, e.g., replacement, of one or both of the
non-linking (X and Y) phosphate oxygens and/or of one or more of
the linking (W and Z) phosphate oxygens (When the phosphate is in
the terminal position, one of the positions W or Z will not link
the phosphate to an additional element in a naturally occurring
ribonucleic acid. However, for simplicity of terminology, except
where otherwise noted, the W position at the 5' end of a nucleic
acid and the terminal Z position at the 3' end of a nucleic acid,
are within the term "linking phosphate oxygens" as used
herein.);
[0080] (ii) alteration, e.g., replacement, of a constituent of the
ribose sugar, e.g., of the 2' hydroxyl on the ribose sugar, or
wholesale replacement of the ribose sugar with a structure other
than ribose, e.g., as described herein;
[0081] (iii) wholesale replacement of the phosphate moiety (bracket
I) with "dephospho" linkers;
[0082] (iv) modification or replacement of a naturally occurring
base;
[0083] (v) replacement or modification of the ribose-phosphate
backbone (bracket II);
[0084] (vi) modification of the 3' end or 5' end of the RNA, e.g.,
removal, modification or replacement of a terminal phosphate group
or conjugation of a moiety, e.g. a fluorescently labeled moiety, to
either the 3' or 5' end of RNA.
[0085] The terms replacement, modification, alteration, and the
like, as used in this context, do not imply any process limitation,
e.g., modification does not mean that one must start with a
reference or naturally occurring ribonucleic acid and modify it to
produce a modified ribonucleic acid but rather modified simply
indicates a difference from a naturally occurring molecule.
[0086] It is understood that the actual electronic structure of
some chemical entities cannot be adequately represented by only one
canonical form (i.e. Lewis structure). While not wishing to be
bound by theory, the actual structure can instead be some hybrid or
weighted average of two or more canonical forms, known collectively
as resonance forms or structures. Resonance structures are not
discrete chemical entities and exist only on paper. They differ
from one another only in the placement or "localization" of the
bonding and nonbonding electrons for a particular chemical entity.
It can be possible for one resonance structure to contribute to a
greater extent to the hybrid than the others. Thus, the written and
graphical descriptions of the embodiments of the present invention
are made in terms of what the art recognizes as the predominant
resonance form for a particular species. For example, any
phosphoroamidate (replacement of a nonlinking oxygen with nitrogen)
would be represented by X.dbd.O and Y.dbd.N in the above
figure.
[0087] Specific modifications are discussed in more detail
below.
[0088] The Phosphate Group
[0089] The phosphate group is a negatively charged species. The
charge is distributed equally over the two non-bridging oxygen
atoms. However, the phosphate group can be modified by replacing
one of the oxygens with a different substituent. One result of this
modification to RNA phosphate backbones can be increased resistance
of the oligoribonucleotide to nucleolytic breakdown. Thus while not
wishing to be bound by theory, it can be desirable in some
embodiments to introduce alterations which result in either an
uncharged bridge or a charged bridge with unsymmetrical charge
distribution.
[0090] Examples of modified phosphate groups include
phosphorothioate, phosphoroselenates, borano phosphates, borano
phosphate esters, hydrogen phosphonates, phosphoroamidates, alkyl
or aryl phosphonates and phosphotriesters. Phosphorodithioates have
both non-linking oxygens replaced by sulfur. Unlike the situation
where only one of the non-bridging oxygens is altered, the
phosphorus center in the phosphorodithioates is achiral which
precludes the formation of oligoribonucleotides diastereomers.
Diastereomer formation can result in a preparation in which the
individual diastereomers exhibit varying resistance to nucleases.
Further, the hybridization affinity of RNA containing chiral
phosphate groups can be lower relative to the corresponding
unmodified RNA species. Thus, while not wishing to be bound by
theory, modifications to both non-bridging oxygens which eliminate
the chiral center, e.g. phosphorodithioate formation, may be
desirable in that they cannot produce diastereomer mixtures. Thus,
either or both of the non-bridging oxygens can be replaced by any
one of S, Se, B, C, H, N, or OR (R is alkyl or aryl). Replacement
with sulfur is preferred.
[0091] The phosphate bridge can also be modified by replacement of
a bridging oxygen with nitrogen (bridged phosphoroamidates), sulfur
(bridged phosphorothioates) and carbon (bridged
methylenephosphonates). The replacement can occur at a terminal
oxygen, e.g. at the 3'- or 5'-terminus. Replacement the 3'-teminus
with carbon or the 5'-terminus with nitrogen is preferred.
[0092] Candidate agents can be evaluated for suitability as
described below.
[0093] The Sugar Group
[0094] A modified RNA can include modification of all or some of
the sugar groups of the ribonucleic acid. E.g., the 2' hydroxyl
group (OH) can be modified or replaced with a number of different
"oxy" or "deoxy" substituents. While not being bound by theory,
enhanced stability is expected since the hydroxyl can no longer be
deprotonated to form a 2' alkoxide ion. The 2' alkoxide can
catalyze degradation by intramolecular nucleophilic attack on the
linker phosphorus atom. Again, while not wishing to be bound by
theory, it can be desirable to some embodiments to introduce
alterations in which alkoxide formation at the 2' position is not
possible.
[0095] Examples of "oxy"-2' hydroxyl group modifications include
alkoxy or aryloxy (OR, e.g., R.dbd.H, alkyl, cycloalkyl, aryl,
aralkyl, heteroaryl or sugar); polyethyleneglycols (PEG),
O(CH.sub.2CH.sub.2O).sub.nCH.sub.2CH.sub.2OR; "locked" nucleic
acids (LNA) in which the 2' hydroxyl is connected, e.g., by a
methylene bridge or ethylene bridge (e.g., 2'-4'-ethylene bridged
nucleic acid (ENA)), to the 4' carbon of the same ribose sugar;
O-AMINE (AMINE=NH.sub.2; alkylamino, dialkylamino, heterocyclyl,
arylamino, diaryl amino, heteroaryl amino, or diheteroaryl amino,
ethylene diamine, polyamino) and aminoalkoxy,
O(CH.sub.2).sub.nAMINE, (e.g., AMINE=NH.sub.2; alkylamino,
dialkylamino, heterocyclyl, arylamino, diaryl amino, heteroaryl
amino, or diheteroaryl amino, ethylene diamine, polyamino). It is
noteworthy that oligonucleotides containing only the methoxyethyl
group (MOE), (OCH.sub.2CH.sub.2OCH.sub.3, a PEG derivative),
exhibit nuclease stabilities comparable to those modified with the
robust phosphorothioate modification.
[0096] "Deoxy" modifications include hydrogen (i.e. deoxyribose
sugars); halo (e.g., fluoro); amino (e.g. NH.sub.2; alkylamino,
dialkylamino, heterocyclyl, arylamino, diaryl amino, heteroaryl
amino, diheteroaryl amino, or amino acid);
NH(CH.sub.2CH.sub.2NH).sub.nCH.sub.2CH.sub.2-AMINE (AMINE=NH.sub.2;
alkylamino, dialkylamino, heterocyclyl, arylamino, diaryl amino,
heteroaryl amino,or diheteroaryl amino), --NHC(O)R (R=alkyl,
cycloalkyl, aryl, aralkyl, heteroaryl or sugar), cyano; mercapto;
alkyl-thio-alkyl; thioalkoxy; and alkyl, cycloalkyl, aryl, alkenyl
and alkynyl, which may be optionally substituted with e.g., an
amino functionality. Preferred substitutents are 2'-methoxyethyl,
2'-OCH.sub.3, 2'-O-allyl, 2'-C-allyl, and 2'-fluoro.
[0097] The sugar group can also contain one or more carbons that
possess the opposite stereochemical configuration than that of the
corresponding carbon in ribose. Thus, a modified RNA can include
nucleotides containing e.g., arabinose, as the sugar.
[0098] Modified RNAs can also include "abasic" sugars, which lack a
nucleobase at C-1'. These abasic sugars can also be further contain
modifications at one or more of the constituent sugar atoms.
[0099] To maximize nuclease resistance, the 2' modifications can be
used in combination with one or more phosphate linker modifications
(e.g., phosphorothioate). The so-called "chimeric" oligonucleotides
are those that contain two or more different modifications.
Chimeric oligonucleotides are well within the bounds of the present
invention.
[0100] The modification can also entail the wholesale replacement
of a ribose structure with another entity at one or more sites in
the RNAi agent.
[0101] Candidate modifications can be evaluated as described
below.
[0102] Replacement of the Phosphate Group
[0103] The phosphate group can be replaced by non-phosphorus
containing connectors. While not wishing to be bound by theory, it
is believed that since the charged phosphodiester group is the
reaction center in nucleolytic degradation, its replacement with
neutral structural mimics should impart enhanced nuclease
stability. Again, while not wishing to be bound by theory, it can
be desirable, in some embodiment, to introduce alterations in which
the charged phosphate group is replaced by a neutral moiety.
[0104] Examples of moieties which can replace the phosphate group
include siloxane, carbonate, carboxymethyl, carbamate, amide,
thioether, ethylene oxide linker, sulfonate, sulfonamide,
thioformacetal, formacetal, oxime, methyleneimino,
methylenemethylimino, methylenehydrazo, methylenedimethylhydrazo
and methyleneoxymethylimino. Preferred replacements include the
methylenecarbonylamino and methylenemethylimino groups.
[0105] Candidate modifications can be evaluated as described
below.
[0106] Replacement of Ribophosphate Backbone
[0107] Oligonucleotide-mimicking scaffolds can also be constructed
wherein the phosphate linker and ribose sugar are replaced by
nuclease resistant nucleoside or nucleotide surrogates. While not
wishing to be bound by theory, it is believed that the absence of a
repetitively charged backbone diminishes binding to proteins that
recognize polyanions (e.g. nucleases). Again, while not wishing to
be bound by theory, it can be desirable in some embodiment, to
introduce alterations in which the bases are linker grouped by a
neutral surrogate backbone.
[0108] Examples include the morphilino, cyclobutyl, pyrrolidine and
peptide nucleic acid (PNA) nucleoside surrogates. A preferred
surrogate is a PNA surrogate.
[0109] Candidate modifications can be evaluated as described
below.
[0110] Terminal Modifications
[0111] The 3' and 5' ends of an oligonucleotide strand can be
modified. Such modifications can be at the 3' end, 5' end or both
ends of the molecule. They can include modification or replacement
of an entire terminal phosphate or of one or more of the atoms of
the phosphate group. E.g., the 3' and 5' ends of an oligonucleotide
can be conjugated to other functional molecular entities such as
labeling moieties, e.g., fluorophores (e.g., pyrene, TAMRA,
fluorescein, Cy3 or Cy5 dyes) or protecting groups (based e.g., on
sulfur, silicon, boron or ester). The functional molecular entities
can be attached to the sugar through a phosphate group and/or a
spacer. The terminal atom of the spacer can connect to or replace
the linking atom of the phosphate group or the C-3' or C-5' O, N, S
or C group of the sugar. Alternatively, the spacer can connect to
or replace the terminal atom of a nucleotide surrogate (e.g.,
PNAs). These spacers or linkers can include e.g.,
--(CH.sub.2).sub.n--, --(CH.sub.2).sub.nN--, --(CH.sub.2).sub.nO--,
--(CH.sub.2).sub.nS--, O(CH.sub.2CH.sub.2O).sub.nCH.sub.2CH.sub.2OH
(e.g., n=3 or 6), abasic sugars, amide, carboxy, amine, oxyamine,
oxyimine, thioether, disulfide, thiourea, sulfonamide, or
morpholino, or biotin and fluorescein reagents. While not wishing
to be bound by theory, it is believed that conjugation of certain
moieties can improve transport, hybridization, and specificity
properties. Again, while not wishing to be bound by theory, it may
be desirable to introduce terminal alterations that improve
nuclease resistance. Other examples of terminal modifications
include dyes, intercalating agents (e.g. acridines), cross-linkers
(e.g. psoralene, mitomycin C), porphyrins (TPPC4, texaphyrin,
Sapphyrin), polycyclic aromatic hydrocarbons (e.g., phenazine,
dihydrophenazine), artificial endonucleases (e.g. EDTA), lipophilic
oligonucleotide strands (e.g., cholesterol, cholic acid, adamantane
acetic acid, 1-pyrene butyric acid, dihydrotestosterone, 1,3
-Bis-O(hexadecyl)glycerol, geranyloxyhexyl group,
hexadecylglycerol, borneol, menthol, 1,3-propanediol, heptadecyl
group, palmitic acid, myristic acid, O3-(oleoyl)lithocholic acid,
O3-(oleoyl)cholenic acid, dimethoxytrityl, or phenoxazine) and
peptide conjugates (e.g., antennapedia peptide, Tat peptide),
alkylating agents, phosphate, amino, mercapto, PEG (e.g., PEG-40K),
MPEG, [MPEG].sub.2, polyamino, alkyl, substituted alkyl,
radiolabeled markers, enzymes, haptens (e.g. biotin),
transport/absorption facilitators (e.g., aspirin, vitamin E, folic
acid), synthetic ribonucleases (e.g., imidazole, bisimidazole,
histamine, imidazole clusters, acridine-imidazole conjugates, Eu3+
complexes of tetraazamacrocycles).
[0112] Terminal modifications can be added for a number of reasons,
including as discussed elsewhere herein to modulate activity or to
modulate resistance to degradation. Preferred modifications include
the addition of a methylphosphonate at the 3'-most terminal
linkage; a 3' C5-aminoalkyl-dT; 3' cationic group; or another 3'
conjugate to inhibit 3'-5' exonucleolytic degradation.
[0113] Terminal modifications useful for modulating activity
include modification of the 5' end with phosphate or phosphate
analogs. E.g., in preferred embodiments RNAi agents are 5'
phosphorylated or include a phosphoryl analog at the 5' terminus.
5'-phosphate modifications include those which are compatible with
RISC mediated gene silencing. Suitable modifications include:
5'-monophosphate ((HO).sub.2(O)P--O-5'); 5'-diphosphate
((HO).sub.2(O)P--O--P(HO)(O)--O-5'); 5'-triphosphate
((HO).sub.2(O)P--O--(HO)(O)P--O--P(HO)(O)--O-5'); 5'-guanosine cap
(7-methylated or non-methylated)
(7m-G-O-5'-(HO)(O)P--O--(HO)(O)P--O--P(HO)(O)--O-5'); 5'-adenosine
cap (Appp), and any modified or unmodified nucleotide cap structure
(N--O-5'-(HO)(O)P--O--(HO)(O)P--O--P(HO)(O)--O-5');
5'-monothiophosphate (phosphorothioate; (HO).sub.2(S)P--O-5');
5'-monodithiophosphate (phosphorodithioate; (HO)(HS)(S)P--O-5'),
5'-phosphorothiolate ((HO).sub.2(O)P--S-5'); any additional
combination of oxgen/sulfur replaced monophosphate, diphosphate and
triphosphates (e.g. 5'-alpha-thiotriphosphate,
5'-gamma-thiotriphosphate, etc.), 5'-phosphoramidates
((HO).sub.2(O)P--NH-5', (HO)(NH.sub.2)(O)P--O-5'),
5'-alkylphosphonates (R=alkyl=methyl, ethyl, isopropyl, propyl,
etc., e.g. RP(OH)(O)--O-5'-, (OH).sub.2(O)P-5'-CH.sub.2--),
5'-alkyletherphosphonates (R=alkylether=methoxymethyl
(MeOCH.sub.2--), ethoxymethyl, etc., e.g. RP(OH)(O)--O-5'-).
[0114] Terminal modifications can also be useful for monitoring
distribution, and in such cases the preferred groups to be added
include fluorophores, e.g., fluorescein or an Alexa dye, e.g.,
Alexa 488. Terminal modifications can also be useful for enhancing
uptake, useful modifications for this include cholesterol. Terminal
modifications can also be useful for cross-linking an RNAi agent to
another moiety; modifications useful for this include mitomycin
C.
[0115] Candidate modifications can be evaluated as described
below.
[0116] The Bases
[0117] Adenine, guanine, cytosine and uracil are the most common
bases found in RNA. These bases can be modified or replaced to
provide RNA's having improved properties. E.g., nuclease resistant
oligoribonucleotides can be prepared with these bases or with
synthetic and natural nucleobases (e.g., inosine, thymine,
xanthine, hypoxanthine, nubularine, isoguanisine, or tubercidine)
and any one of the above modifications. Alternatively, substituted
or modified analogs of any of the above bases, e.g., "unusual
bases" and "universal bases" can be employed. Examples include
without limitation 2-aminoadenine, 6-methyl and other alkyl
derivatives of adenine and guanine, 2-propyl and other alkyl
derivatives of adenine and guanine, 5-halouracil and cytosine,
5-propynyl uracil and cytosine, 6-azo uracil, cytosine and thymine,
5-uracil (pseudouracil), 4-thiouracil, 5-halouracil,
5-(2-aminopropyl)uracil, 5-amino allyl uracil, 8-halo, amino,
thiol, thioalkyl, hydroxyl and other 8-substituted adenines and
guanines, 5-trifluoromethyl and other 5-substituted uracils and
cytosines, 7-methylguanine, 5-substituted pyrimidines,
6-azapyrimidines and N-2, N-6 and O-6 substituted purines,
including 2-aminopropyladenine, 5-propynyluracil and
5-propynylcytosine, dihydrouracil, 3-deaza-5-azacytosine,
2-aminopurine, 5-alkyluracil, 7-alkylguanine, 5-alkyl
cytosine,7-deazaadenine, N6, N6-dimethyladenine, 2,6-diaminopurine,
5-amino-allyl-uracil, N3-methyluracil, substituted 1,2,4-triazoles,
2-pyridinone, 5-nitroindole, 3-nitropyrrole, 5-methoxyuracil,
uracil-5-oxyacetic acid, 5-methoxycarbonylmethyluracil,
5-methyl-2-thiouracil, 5-methoxycarbonylmethyl-2-thiouracil,
5-methylaminomethyl-2-thiouracil, 3-(3-amino-3carboxypropyl)uracil,
3-methylcytosine, 5-methyl cytosine, N.sup.4-acetyl cytosine,
2-thiocytosine, N6-methyladenine, N6-isopentyladenine,
2-methylthio-N6-isopentenyladenine, N-methylguanines, or
O-alkylated bases. Further purines and pyrimidines include those
disclosed in U.S. Pat. No. 3,687,808, those disclosed in the
Concise Encyclopedia Of Polymer Science And Engineering, pages
858-859, Kroschwitz, J. I., ed. John Wiley & Sons, 1990, and
those disclosed by Englisch et al., Angewandte Chemie,
International Edition, 1991, 30, 613.
[0118] Generally, base changes are less preferred for promoting
stability, but they can be useful for other reasons, e.g., some,
e.g., 2,6-diaminopurine and 2 amino purine (e.g., 2-amino adenine),
are fluorescent. Modified bases can reduce target specificity. This
should be taken into consideration in the design of RNAi
agents.
[0119] Candidate modifications can be evaluated as described
below.
[0120] Evaluation of Candidate RNAi Agents
[0121] One can evaluate a candidate RNAi agent, e.g., a modified
RNAi agent, for a selected property by exposing the agent or
modified molecule and a control molecule to the appropriate
conditions and evaluating for the presence of the selected
property. For example, resistance to a degradent can be evaluated
as follows. A candidate modified RNA (and preferably a control
molecule, usually the unmodified form) can be exposed to
degradative conditions, e.g., exposed to a milieu, which includes a
degradative agent, e.g., a nuclease. E.g., one can use a biological
sample, e.g., one that is similar to a milieu, which might be
encountered, in therapeutic use, e.g., blood or serum, or a
cellular fraction, e.g., a cell-free homogenate or disrupted cells.
The candidate and control could then be evaluated for resistance to
degradation by any of a number of approaches. For example, the
candidate and control could be labeled, preferably prior to
exposure, with, e.g., a radioactive or enzymatic label, or a
fluorescent label, such as Cy3 or Cy5. Control and modified RNA's
can be incubated with the degradative agent, and optionally a
control, e.g., an inactivated, e.g., heat inactivated, degradative
agent. A physical parameter, e.g., size, of the modified and
control molecules are then determined. They can be determined by a
physical method, e.g., by polyacrylamide gel electrophoresis or a
sizing column, to assess whether the molecule has maintained its
original length, or assessed functionally. Alternatively, Northern
blot analysis or mass spectrometry can be used to assay the length
of an unlabeled modified molecule.
[0122] A functional assay can also be used to evaluate the
candidate agent. A functional assay can be applied initially or
after an earlier non-functional assay, (e.g., assay for resistance
to degradation) to determine if the modification alters the ability
of the molecule to inhibit gene expression. For example, a cell,
e.g., a mammalian cell, such as a mouse or human cell, can be
co-transfected with a plasmid expressing a fluorescent protein,
e.g., GFP, and a candidate RNAi agent homologous to the transcript
encoding the fluorescent protein (see, e.g., WO 00/44914). For
example, a modified RNAi agent homologous to the GFP mRNA can be
assayed for the ability to inhibit GFP expression by monitoring for
a decrease in cell fluorescence, as compared to a control cell, in
which the transfection did not include the candidate RNAi agent,
e.g., controls with no agent added and/or controls with a
non-modified RNA added. Efficacy of the candidate agent on gene
expression can be assessed by comparing cell fluorescence in the
presence of the modified and unmodified RNAi agent. In an
alternative functional assay, a candidate RNAi agent homologous to
an endogenous mouse gene, preferably a maternally expressed gene,
such as c-mos, can be injected into an immature mouse oocyte to
assess the ability of the agent to inhibit gene expression in vivo
(see, e.g., WO 01/36646). A phenotype of the oocyte, e.g., the
ability to maintain arrest in metaphase II, can be monitored as an
indicator that the agent is inhibiting expression. For example,
cleavage of c-mos mRNA by an RNAi agent would cause the oocyte to
exit metaphase arrest and initiate parthenogenetic development
(Colledge et al. Nature 370: 65-68, 1994; Hashimoto et al. Nature,
370:68-71, 1994). The effect of the modified agent on target RNA
levels can be verified by Northern blot to assay for a decrease in
the level of target RNA, or by Western blot to assay for a decrease
in the level of target protein, as compared to a negative control.
Controls can include cells in which with no agent is added and/or
cells in which a non-modified RNA is added.
[0123] An RNAi agent that targets an miRNA ore pre-miRNA can be
assayed by monitoring expression of the transcript targeted by the
miRNA. For example, an RNAi agent designed to bind an miRNA that
targets GFP can be assessed by monitoring for an increase in cell
fluorescence, as compared to a control cell, in which the
transfection did not include the candidate RNAi agent, e.g.,
controls with no agent added and/or controls with a non-modified
RNA added. In another example, an RNAi agent designed to bind an
miRNA that targets an endogenous enzyme can be assessed by
monitoring for an increase in enzyme activity, as compared to a
control cell. The effect of the modified RNAi agent on target miRNA
levels can be verified by Northern blot to assay for a decrease in
the level of the target miRNA.
Exemplary Embodiments
[0124] One aspect the invention provides an RNAi agent for
inhibiting the expression of a target gene in a cell, wherein the
RNAi agent consists essentially of an oligoribonucleotide strand of
between 15 and 30 nucleotides in length, wherein said
oligoribonucleotide strand is coupled via a linker to a ligand of
formula (I)
##STR00002##
[0125] wherein n is 1-20;
[0126] R.sup.1, R.sup.3, R.sup.4 and R.sup.6 are each independently
for each occurrence H, a phosphate group, a ligand of formula (I),
a C.sub.1-C.sub.6 alkyoxy, a C.sub.1-C.sub.6 acyloxy,
##STR00003##
a carbohydrate or
##STR00004##
provided that at least one of R.sup.1, R.sup.3, R.sup.4 and R.sup.6
is
##STR00005##
[0127] R.sup.2 and R.sup.7 are each independently for each
occurrence OH or NHCH.sub.2COOH;
[0128] R.sup.8, R.sup.9 and R.sup.10 are independently for each
occurrence H, a phosphate group, a ligand of formula (I), a
C.sub.1-C.sub.6 alkyoxy, a C.sub.1-C.sub.6 acyloxy, a
carbohydrate,
##STR00006##
[0129] the linker is linear, branched, or a bond;
[0130] Z.sup.1 and Z.sup.2 are independently O, S, OH, O.sup.-,
OR.sup.11 , Se, BH.sub.3.sup.-, H, NHR.sup.12, N(R.sup.12).sub.2,
optionally substituted alkyl, optionally substituted cycloalkyl,
optionally substituted aralkyl, optionally substituted aryl, or
optionally substituted heteroaryl;
[0131] R.sup.11 and R.sup.12 are each independently for each
occurrence optionally substituted alkyl, optionally substituted
cycloalkyl, optionally substituted aryl, optionally substituted
aralkyl, optionally substituted heterocyclyl, optionally
substituted heteroaryl or amino acid;
[0132] wherein said oligoribonucleotide strand is complementary to
at least one portion of an mRNA corresponding to the target
gene.
[0133] In one embodiment R.sup.1, R.sup.3, R.sup.4 and R.sup.6 are
each independently for each occurrence H, a phosphate group, a
ligand of formula (I), a C.sub.1-C.sub.6 alkyoxy, a C.sub.1-C.sub.6
acyloxy or
##STR00007##
and Z.sup.1 and Z.sup.2 are independently O or S.
[0134] In a preferred embodiment the formula (I) has the
structure
##STR00008##
wherein R.sup.6 is H, a phosphate group, or a ligand of formula (I)
and R.sup.1 is
##STR00009##
[0135] In one embodiment the branched linker has a structure of
formula (III)
##STR00010##
[0136] wherein Z.sup.3 and Z.sup.4 are independently independently
O, S, OH, O.sup.-, OR.sup.11 , Se, BH.sub.3.sup.-, H, NHR12.sub.,
N(R.sup.12).sub.2, optionally substituted alkyl, optionally
substituted cycloalkyl, optionally substituted aralkyl, optionally
substituted aryl, or optionally substituted heteroaryl;
[0137] R.sup.11 and R.sup.12 are each independently for each
occurrence optionally substituted alkyl, optionally substituted
cycloalkyl, optionally substituted aryl, optionally substituted
aralkyl, optionally substituted heterocyclyl, optionally
substituted heteroaryl or amino acid. In a preferred embodiment,
Z.sup.3 and Z.sup.4 are independently O or S.
[0138] In one embodiment, the intervening linker has a structure of
formula (IV)
igand-O--CH.sub.2CH.sub.2(OCH.sub.2CH.sub.2).sub.nOP(Z.sup.5)(Z.sup.6)O--
branched-linker Formula (IV)
[0139] wherein n is 1-20; and
[0140] Z.sup.5 and Z.sup.6 are each independently independently O,
S, OH, O.sup.-, OR.sup.11, Se, BH.sub.3.sup.-, H, NHR.sup.12,
N(R.sup.12).sub.2, optionally substituted alkyl, optionally
substituted cycloalkyl, optionally substituted aralkyl, optionally
substituted aryl, or optionally substituted heteroaryl;
[0141] R.sup.11 and R.sup.12 are each independently for each
occurrence optionally substituted alkyl, optionally substituted
cycloalkyl, optionally substituted aryl, optionally substituted
aralkyl, optionally substituted heterocyclyl, optionally
substituted heteroaryl or amino acid. In a preferred embodiment
Z.sup.5 and Z.sup.6 are independently O or S.
[0142] In certain embodiments, the present invention relates to the
aforementioned RNAi agent, wherein n is 3. In certain embodiments,
the present invention relates to the aforementioned RNAi agent,
wherein at least one of Z.sup.5 and Z.sup.6 is S. In certain
embodiments, the present invention relates to the aforementioned
RNAi agent, wherein both of Z.sup.5 and Z.sup.6 are O.
[0143] In certain embodiments, the present invention relates to the
aforementioned RNAi agent, wherein the distance between the
galactose moieties is at least about 4 .ANG., at least about 10
.ANG., at least about 15 .ANG., or at least about 20 .ANG..
[0144] In certain embodiments, the present invention relates to the
aforementioned RNAi agent, wherein the RNAi agent is capable of
inhibiting the expression of the target gene in the cell.
[0145] In certain embodiments, the present invention relates to the
aforementioned RNAi agent, wherein the cell harbors an
asialoglycoprotein receptor on its surface.
[0146] In certain embodiments, the present invention relates to the
aforementioned RNAi agent, wherein the cell is a hepatocyte.
[0147] Another aspect of the invention provides an RNAi agent for
inhibiting the expression of a target gene in a cell, wherein the
RNAi agent consists essentially of two mutually complementary
oligoribonucleotide strands of between 15 and 30 nucleotides in
length, wherein at least one of the oligoribonucleotide strands is
coupled via a linker to a ligand of formula (I)
##STR00011##
[0148] wherein n is 1-20;
[0149] R.sup.1, R.sup.3, R.sup.4 and R.sup.6 are each independently
for each occurrence H, a phosphate group, a
[0150] ligand of formula (I), a C.sub.1-C.sub.6 alkyoxy, a
C.sub.1-C.sub.6 acyloxy,
##STR00012##
a carbohydrate or
##STR00013##
provided that at least one of R.sup.1, R.sup.3, R.sup.4 and R.sup.6
is
##STR00014##
[0151] R.sup.2 and R.sup.7 are each independently for each
occurrence OH or NHCH.sub.2COOH;
[0152] R.sup.8, R.sup.9 and R.sup.10 are independently for each
occurrence H, a phosphate group, a ligand of formula (I), a
C.sub.1-C.sub.6 alkyoxy, a C.sub.1-C.sub.6 acyloxy,
##STR00015##
a carbohydrate or
##STR00016##
[0153] the linker is linear, branched, or a bond;
[0154] Z.sup.1 and Z.sup.2 are independently O, S, OH, O.sup.-,
OR.sup.11 , Se, BH.sub.3.sup.-, H, NHR.sup.12, N(R.sup.12).sub.2,
optionally substituted alkyl, optionally substituted cycloalkyl,
optionally substituted aralkyl, optionally substituted aryl, or
optionally substituted heteroaryl;
[0155] R.sup.11 and R.sup.12 are each independently for each
occurrence optionally substituted alkyl, optionally substituted
cycloalkyl, optionally substituted aryl, optionally substituted
aralkyl, optionally substituted heterocyclyl, optionally
substituted heteroaryl or amino acid;
[0156] wherein at least one oligoribonucleotide strand is
complementary to at least one portion of an mRNA corresponding to
the target gene.
[0157] In one embodiment R.sup.1, R.sup.3, R.sup.4 and R.sup.6 are
each independently for each occurrence H, a phosphate group, a
ligand of formula (I), a C.sub.1-C.sub.6 alkyoxy, a C.sub.1-C.sub.6
acyloxy or
##STR00017##
and Z.sup.1 and Z.sup.2 are independently O or S.
[0158] In a preferred embodiment the formula (I) has the
structure
##STR00018##
wherein R.sup.6 is H, a phosphate group, or a ligand of formula (I)
and R.sup.1 is
##STR00019##
[0159] In one embodiment the branched linker has a structure of
formula (III)
##STR00020##
[0160] wherein Z.sup.3 and Z.sup.4 are independently independently
O, S, OH, O.sup.-, OR.sup.11 , Se, BH3.sup.-, H, NHR.sup.12,
N(R.sup.12).sub.2, optionally substituted alkyl, optionally
substituted cycloalkyl, optionally substituted aralkyl, optionally
substituted aryl, or optionally substituted heteroaryl;
[0161] R.sup.11 and R.sup.12 are each independently for each
occurrence optionally substituted alkyl, optionally substituted
cycloalkyl, optionally substituted aryl, optionally substituted
aralkyl, optionally substituted heterocyclyl, optionally
substituted heteroaryl or amino acid. In a preferred embodiment,
Z.sup.3 and Z.sup.4 are independently O or S.
[0162] In one embodiment, the intervening linker has a structure of
formula (IV)
ligand-O
--CH.sub.2CH.sub.2(OCH.sub.2CH.sub.2).sub.nOP(Z.sup.5)(Z.sup.6)-
O-branched-linker Formula (IV)
[0163] wherein n is 1-20; and
[0164] Z.sup.5 and Z.sup.6 are each independently independently O,
S, OH, O.sup.-, OR.sup.11 , Se, BH.sub.3.sup.-, H, NHR.sup.12,
N(R.sup.12).sub.2, optionally substituted alkyl, optionally
substituted cycloalkyl, optionally substituted aralkyl, optionally
substituted aryl, or optionally substituted heteroaryl;
[0165] R.sup.11 and R.sup.12 are each independently for each
occurrence optionally substituted alkyl, optionally substituted
cycloalkyl, optionally substituted aryl, optionally substituted
aralkyl, optionally substituted heterocyclyl, optionally
substituted heteroaryl or amino acid. In a preferred embodiment
Z.sup.5 and Z.sup.6 are independently O or S.
[0166] In certain embodiments, the present invention relates to the
aforementioned RNAi agent, wherein n is 3. In certain embodiments,
the present invention relates to the aforementioned RNAi agent,
wherein at least one of Z.sup.5 and Z.sup.6 is S. In certain
embodiments, the present invention relates to the aforementioned
RNAi agent, wherein both of Z.sup.5 and Z.sup.6 are O.
[0167] In certain embodiments, the present invention relates to the
aforementioned RNAi agent, wherein the distance between the
galactose moieties is at least about 4 .ANG., at least about 10
.ANG., at least about 15 .ANG., or at least about 20 .ANG..
[0168] In certain embodiments, the present invention relates to the
aforementioned RNAi agent, wherein the RNAi agent is capable of
inhibiting the expression of the target gene in the cell.
[0169] In certain embodiments, the present invention relates to the
aforementioned RNAi agent, wherein the cell harbors an
asialoglycoprotein receptor on its surface.
[0170] In certain embodiments, the present invention relates to the
aforementioned RNAi agent, wherein the cell is a hepatocyte.
[0171] In certain embodiments, the present invention relates to any
one of the aforementioned RNAi agents, wherein n is 1, 2, 3, 4, 5
or 6.
[0172] In certain embodiments, the present invention relates to any
one of the aforementioned RNAi agents, wherein n is 4.
[0173] In certain embodiments, the present invention relates to any
one of the aforementioned RNAi agents, wherein at least one of
Z.sup.1 and Z.sup.2 is S.
[0174] In certain embodiments, the present invention relates to any
one of the aforementioned RNAi agents, wherein both of Z.sup.1 and
Z.sup.2 are O.
[0175] In certain embodiments, the present invention relates to any
one of the aforementioned RNAi agents, wherein at least one the
oligoribonucleotide strands comprises at least one phosphorothioate
linkage.
[0176] In certain embodiments, the present invention relates to any
one of the aforementioned RNAi agents, wherein at least one of the
oligoribonucleotide strands comprises at least one nucleotide with
a 2'-modification. In certain embodiments, the present invention
relates to any one of the aforementioned RNAi agents, wherein the
2'-modification comprises one of 2'-H, 2'-O-methyl,
2'-O-methoxyethyl, 2'-O-aminopropyl, 2'-Fluoro, 2'-O
--CH.sub.2--CO-NHMe,
2'-O--CH.sub.2CH.sub.2OCH.sub.2CH.sub.2N(Me).sub.2, 2'-4'-methylene
(LNA), 2'-4'-ethylene (ENA), 2'-S-methyl, 2'-ara-fluoro,
2'-O-allyl, 2'-C-allyl, 2'-O-NH.sub.2, 2'-NH.sub.2 and
2'-ethynyl.
[0177] Another aspect of the invention relates to a pharmaceutical
composition, comprising (i) any one of the aforementioned RNAi
agents; and (ii) a pharmaceutically acceptable excipient.
[0178] Another aspect of the invention relates to a method for the
manufacture of an RNAi agent of any one of the aforementioned RNAi
agents, comprising the steps of (i) synthesizing two mutually
complementary oligoribonucleotide strands of between 15 and 30
nucleotides in length, wherein at least one of the
oligoribonucleotides is coupled to a ligand comprising a linker
group and at least one galactose moiety; and (ii) effecting the
hybridization of the at least two mutually complementary
oligoribonucleotides. In certain embodiments, the present invention
relates to the aforementioned method of manufacture, further
comprising the step of formulating the RNAi agent with a
pharmaceutically acceptable excipient.
[0179] Another aspect of the invention relates to a method to
introduce an RNAi agent into a cell, comprising the step of
contacting the cell with the RNAi agent of the present invention.
In certain embodiments, the cell is a hepatocyte.
[0180] Another aspect of the invention relates to a method of
treatment, comprising a step of administering to a subject in need
thereof a therapeutically effective amount of a pharmaceutical
composition of the present invention. In certain embodiments, the
subject is in need of a treatment for a disease or condition
related to unwanted expression of a target gene in the liver. In
certain embodiments, the subject is a vertebrate, mammal, or
human.
[0181] Another aspect of the invention relates to a cell,
comprising an RNAi agent of the present invention. In certain
embodiments, the cell is a hepatocyte.
[0182] Methods for Making Oligonucleotide Agents
[0183] A listing of ribonucleosides containing the ribonucleosides
described herein are described in "The RNA Modification Database"
maintained by Pamela F. Crain, Jef Rozenski and James A. McCloskey;
Departments of Medicinal Chemistry and Biochemistry, University of
Utah, Salt Lake City, Utah 84112, USA.
[0184] The 5' silyl protecting group can be used in conjunction
with acid labile orthoesters at the 2' position of ribonucleosides
to synthesize oligonucleotides via phosphoramidite chemistry. Final
deprotection conditions are known not to significantly degrade RNA
products. Functional groups on the unusual and universal bases are
blocked during oligonucleotide synthesis with protecting groups
that are compatible with the operations being performed that are
described herein. All syntheses can be conducted in any automated
or manual synthesizer on large, medium, or small scale. The
syntheses may also be carried out in multiple well plates or glass
slides.
[0185] The 5'-O-silyl group can be removed via exposure to fluoride
ions, which can include any source of fluoride ion, e.g., those
salts containing fluoride ion paired with inorganic counterions
e.g., cesium fluoride and potassium fluoride or those salts
containing fluoride ion paired with an organic counterion, e.g., a
tetraalkylammonium fluoride. A crown ether catalyst can be utilized
in combination with the inorganic fluoride in the deprotection
reaction. Preferred fluoride ion source are tetrabutylammonium
fluoride or aminehydrofluorides (e.g., combining aqueous HF with
triethylamine in a dipolar aprotic solvent, e.g.,
dimethylformamide).
[0186] The choice of protecting groups for use on the phosphite
triesters and phosphotriesters can alter the stability of the
triesters towards fluoride. Methyl protection of the
phosphotriester or phosphitetriester can stabilize the linkage
against fluoride ions and improve process yields.
[0187] Since ribonucleosides have a reactive 2' hydroxyl
substituent, it can be desirable to protect the reactive 2'
position in RNA with a protecting group that is compatible with a
5'-O-silyl protecting group, e.g. one stable to fluoride.
Orthoesters meet this criterion and can be readily removed in a
final acid deprotection step that can result in minimal RNA
degradation.
[0188] Tetrazole catalysts can be used in the standard
phosphoramidite coupling reaction. Preferred catalysts include e.g.
tetrazole, S-ethyl-tetrazole, p-nitrophenyltetrazole.
[0189] The general process is as follows. Nucleosides are suitably
protected and functionalized for use in solid-phase or
solution-phase synthesis of RNA oligonucleotides. The 2'-hydroxyl
group in a ribonucleotide can be modified using a tris orthoester
reagent. The 2'-hydroxyl can be modified to yield a 2'-O-orthoester
nucleoside by reacting the ribonucleoside with the tris orthoester
reagent in the presence of an acidic catalyst, e.g., pyridinium
p-toluene sulfonate. This reaction is known to those skilled in the
art. The product can then be subjected to further protecting group
reactions (e.g., 5'-O-silylation) and functionalizations (e.g.,
3'-O-phosphitylation) to produce a desired reagent (e.g.,
nucleoside phosphoramidite) for incorporation within an
oligonucleotide or polymer by reactions known to those skilled in
the art.
[0190] Preferred orthoesters include those comprising ethylene
glycol ligands which are protected with acyl or ester protecting
groups. Specifically, the preferred acyl group is acetyl. The
nucleoside reagents may then be used by those skilled in the art to
synthesize RNA oligonucleotides on commercially available
synthesizer instruments, e.g., Gene Assembler Plus (Pharmacia),
380B (Applied Biosystems). Following synthesis (either
solution-phase or solid-phase) of an oligonucleotide or polymer,
the product can be subjected to one or more reactions using
non-acidic reagents. One of these reactions may be strong basic
conditions, for example, 40% methylamine in water for 10 minutes at
55.degree. C., which will remove the acyl protecting groups from
the ethylene glycol ligands but leave the orthoester moiety
attached. The resultant orthoester may be left attached when the
polymer or oligonucleotide is used in subsequent applications, or
it may be removed in a final mildly-acidic reaction, for example,
10 minutes at 55.degree. C. in 50 mM acetic acid, pH 3.0, followed
by addition of equal volume of 150 mM TRIS buffer for 10 minutes at
55.degree. C.
[0191] Universal bases are described in "Survey and Summary: The
Applications of Universal DNA base analogues" Loakes, D., Nucleic
Acid Research 2001, 29, 2437, which is incorporated by reference in
its entirety. Specific examples are described in the following:
Liu, D.; Moran, S.; Kool, E. T. Chem. Biol., 1997, 4, 919-926;
Morales, J. C.; Kool, E. T. Biochemistry, 2000, 39, 2626-2632;
Matray, T, J.; Kool, E. T. J. Am. Chem. Soc., 1998, 120, 6191-6192;
Moran, S. Ren, R. X.-F.; Rumney IV, S.; Kool, E. T. J. Am. Chem.
Soc., 1997, 119, 2056-2057; Guckian, K. M.; Morales, J. C.; Kool,
E. T. J. Org. Chem., 1998, 63, 9652-9656; Berger, M.; Wu. Y.;
Ogawa, A. K.; McMinn, D. L.; Schultz, P. G.; Romesberg, F. E.
Nucleic Acids Res., 2000, 28, 2911-2914; Ogawa, A. K.; Wu, Y.;
McMinn, D. L.; Liu, J.; Schultz, P. G.; Romesberg, F. E. J. Am.
Chem. Soc., 2000, 122, 3274-3287; Ogawa, A. K.; Wu. Y.; Berger, M.;
Schultz, P. G.; Romesberg, F. E. J. Am. Chem. Soc., 2000, 122,
8803-8804; Tae, E. L.; Wu, Y.; Xia, G.; Schultz, P. G.; Romesberg,
F. E. J. Am. Chem. Soc., 2001, 123, 7439-7440; Wu, Y.; Ogawa, A.
K.; Berger, M.; McMinn, D. L.; Schultz, P. G.; Romesberg, F. E. J.
Am. Chem. Soc., 2000, 122, 7621-7632; . McMinn, D. L.; Ogawa. A.
K.; Wu, Y.; Liu, J.; Schultz, P. G.; Romesberg, F. E. J. Am. Chem.
Soc., 1999, 121, 11585-11586; Brotschi, C.; Haberli, A.; Leumann,
C, J. Angew. Chem. Int. Ed., 2001, 40, 3012-3014; Weizman, H.; Tor,
Y. J. Am. Chem. Soc., 2001, 123, 3375-3376; Lan, T.; McLaughlin, L.
W. J. Am. Chem. Soc., 2000, 122, 6512-13.
[0192] As discussed above, the monomers and methods described
herein can be used in the preparation of modified RNA molecules, or
polymeric molecules comprising any combination of monomer compounds
described herein and/or natural or modified ribonucleotides.
Modified RNA molecules include e.g. those molecules containing a
chemically or stereochemically modified nucleoside (e.g., having
one or more backbone modifications, e.g., phosphorothioate or
P-alkyl; having one or more sugar modifications, e.g., 2'-OCH.sub.3
or 2'-F; and/or having one or more base modifications, e.g.,
5-alkylamino or 5-allylamino) or a nucleoside surrogate.
[0193] Coupling of 5'-hydroxyl groups with phosphoramidites forms
phosphite ester intermediates, which in turn are oxidized e.g.,
with iodine, to the phosphate diester. Alternatively, the
phosphites may be treated with, e.g., sulfur, selenium, amino, and
boron reagents to form modified phosphate backbones. Linkages
between the monomers described herein and a nucleoside or
oligonucleotide chain can also be treated with iodine, sulfur,
selenium, amino, and boron reagents to form unmodified and modified
phosphate backbones respectively. Similarly, the monomers described
herein may be coupled with nucleosides or oligonucleotides
containing any of the modifications or nucleoside surrogates
described herein.
[0194] The synthesis and purification of oligonucleotide conjugates
can be performed by established methods. See, for example, Trufert
et al., Tetrahedron, 52:3005, 1996; and Manoharan, "Oligonucleotide
Conjugates in Antisense Technology," in Antisense Drug Technology,
ed. S. T. Crooke, Marcel Dekker, Inc., 2001. The protected monomer
compounds can be separated from a reaction mixture and further
purified by a method such as column chromatography, high pressure
liquid chromatography, or recrystallization. As can be appreciated
by the skilled artisan, further methods of synthesizing the
compounds of the formulae herein will be evident to those of
ordinary skill in the art. Additionally, the various synthetic
steps may be performed in an alternate sequence or order to give
the desired compounds. Other synthetic chemistry transformations,
protecting groups (e.g., for hydroxyl, amino, etc. present on the
bases) and protecting group methodologies (protection and
deprotection) useful in synthesizing the compounds described herein
are known in the art and include, for example, those such as
described in R. Larock, Comprehensive Organic Transformations, VCH
Publishers (1989); T. W. Greene and P. G. M. Wuts, Protective
Groups in Organic Synthesis, 2d. Ed., John Wiley and Sons (1991);
L. Fieser and M. Fieser, Fieser and Fieser's Reagents for Organic
Synthesis, John Wiley and Sons (1994); and L. Paquette, ed.,
Encyclopedia of Reagents for Organic Synthesis, John Wiley and Sons
(1995), and subsequent editions thereof.
[0195] The protected monomer compounds of this invention may
contain one or more asymmetric centers and thus occur as racemates
and racemic mixtures, single enantiomers, individual diastereomers
and diastereomeric mixtures. All such isomeric forms of these
compounds are expressly included in the present invention. The
compounds described herein can also contain linkages (e.g.,
carbon-carbon bonds, carbon-nitrogen bonds, e.g., amides) or
substituents that can restrict bond rotation, e.g. restriction
resulting from the presence of a ring or double bond. Accordingly,
all cis/trans, E/Z isomers, and rotational isomers (rotamers) are
expressly included herein. The compounds of this invention may also
be represented in multiple tautomeric forms, in such instances, the
invention expressly includes all tautomeric forms of the compounds
described herein (e.g., alkylation of a ring system may result in
alkylation at multiple sites, the invention expressly includes all
such reaction products). All such isomeric forms of such compounds
are expressly included in the present invention. All crystal forms
of the compounds described herein are expressly included in the
present invention.
[0196] Formulation
[0197] The RNAi agents described herein can be formulated for
administration to a subject.
[0198] For ease of exposition the formulations, compositions and
methods in this section are discussed largely with regard to
unmodified RNAi agents. It should be understood, however, that
these formulations, compositions and methods can be practiced with
other RNAi agents, e.g., modified RNAi agents, and such practice is
within the invention.
[0199] A formulated RNAi agent composition can assume a variety of
states. In some examples, the composition is at least partially
crystalline, uniformly crystalline, and/or anhydrous (e.g., less
than 80, 50, 30, 20, or 10% water). In another example, the RNAi
agent is in an aqueous phase, e.g., in a solution that includes
water.
[0200] The aqueous phase or the crystalline compositions can, e.g.,
be incorporated into a delivery vehicle, e.g., a liposome
(particularly for the aqueous phase) or a particle (e.g., a
microparticle as can be appropriate for a crystalline composition).
Generally, the RNAi agent composition is formulated in a manner
that is compatible with the intended method of administration (see,
below).
[0201] In particular embodiments, the composition is prepared by at
least one of the following methods: spray drying, lyophilization,
vacuum drying, evaporation, fluid bed drying, or a combination of
these techniques; or sonication with a lipid, freeze-drying,
condensation and other self-assembly.
[0202] An RNAi agent preparation can be formulated in combination
with another agent, e.g., another therapeutic agent or an agent
that stabilizes an RNAi agent, e.g., a protein that complexes with
an RNAi agent. Still other agents include chelators, e.g., EDTA
(e.g., to remove divalent cations such as Mg.sup.2+), salts, RNAse
inhibitors (e.g., a broad specificity RNAse inhibitor such as
RNAsin) and so forth.
[0203] In one embodiment, the RNAi agent preparation includes a
second RNAi agent, e.g., a second RNAi agent that can modulate gene
expression with respect to a second gene, or with respect to the
same gene. Still other preparation can include at least three,
five, ten, twenty, fifty, or a hundred or more different RNAi agent
species. Such RNAi agents can modulate gene expression with respect
to a similar number of different genes.
[0204] In one embodiment, the RNAi agent preparation includes at
least a second therapeutic agent (e.g., an agent other than an RNA
or a DNA). For example, an RNAi agent composition for the treatment
of a viral disease, e.g. HCV, might include a known antiviral agent
(e.g., a protease inhibitor). In another example, an RNAi agent
composition for the treatment of a cancer might further comprise a
chemotherapeutic agent. In a preferred embodiment, the
pharmaceutical composition includes an additive that stimulates the
expression, activity and/or affinity of the asialoglycoprotein
receptor for the binding of the RNAi agent. For example, the
additive may result in an increase of the calcium concentrations in
the liver. An increased calcium concentration in the liver may
enhance the expression of the asialoglycoprotein receptor, and
increase the number of receptor molecules present on hepatocytes as
compared to a delivery of the RNAi agent without the additive.
[0205] RNAi agents described herein can be formulated for delivery
in a membranous molecular assembly, e.g., a liposome or a micelle.
In one embodiment, a preparation including an RNAi agent can be
formulated as an emulsion that includes a surfactant.
[0206] Targeting to the Liver
[0207] Aspects of the invention relate to silencing genes expressed
in the liver, or to upregulating genes that are regulated by one or
more endogenous miRNAs. Accordingly, the invention includes
compositions and methods for delivering RNAi agents to the liver,
e.g., to treat disorders of or related to the liver.
[0208] An RNAi agent composition of the invention can be one that
has been modified to alter distribution in favor of the liver. A
composition of the invention includes an RNAi agent, e.g., an RNAi
agent described herein.
[0209] Preferably, an RNAi agent of the invention is designed to be
effective as a treatment for one or more adverse conditions or
diseases of the liver, e.g. Alagille syndrome, alcoholic liver
disease, alpha-1-antitrypsin deficiency, Budd-Chiari syndrome,
biliary atresia, Byler disease, dyslipidemias, Caroli-disease,
Crigler-Najjar Syndrome, Dubin-Johnson Syndrome, fatty liver,
galactosemia, Gilbert syndrome, glycogen storage disease I,
hemangioma, hemochromatosis, hepatitis of viral or autoimmune
etiology, liver cancer, liver fibrosis and cirrhosis, porphyria
cutanea tarda, erythrohepatic protoporphyria, Rotor syndrome,
sclerosing cholangitis, or Wilson disease.
[0210] For example, an RNAi agent directed to the liver can target
apoB-100 to treat a disorder characterized by elevated or otherwise
unwanted expression of apoB-100, elevated or otherwise unwanted
levels of cholesterol, and/or disregulation of lipid metabolism.
The RNAi agent can be administered to an individual at risk for the
disorder to delay onset of the disorder or a symptom of the
disorder. These disorders include HDL/LDL cholesterol imbalance;
dyslipidemias, e.g., familial combined hyperlipidemia (FCHL),
acquired hyperlipidemia; hypercholestorolemia; statin-resistant
hypercholesterolemia; coronary artery disease (CAD) coronary heart
disease (CHD) atherosclerosis. In one embodiment, the RNAi agent
that targets apoB-100 is administered to a subject diagnosed as
having statin-resistant hypercholesterolemia.
[0211] The apoB-100 RNAi agent can be administered in an amount
sufficient to reduce levels of serum LDL --C and/or HDL --C and/or
total cholesterol in a subject. In one embodiment, the RNAi agent
is administered in an amount sufficient to reduce the risk of
myocardial infarction the subject.
[0212] In one embodiment, expression levels of apoB-100 are
decreased in the liver following administration of the apoB-100
RNAi agent. For example, the RNAi agent can be complexed with a
moiety that targets the liver, e.g., an antibody or ligand that
binds a receptor on the liver.
[0213] In other embodiments, an RNAi agent targeted to the liver
can modulate expression of, e.g., beta-catenin or
glucose-6-phosphatase RNA, to treat a liver-related disorder.
[0214] In another embodiment, the RNAi agent targets an miRNA or
pre-miRNA expressed in the liver. In another embodiment, the human
is suffering from a disorder characterized by overexpression or
accumulation of the miRNA in the liver, or decreased expression of
a nucleic acid that is the target of the miRNA expressed in the
liver. Administration of the RNAi agent to the subject, or to a
cell of the lung of the subject, can result in the pairing of the
RNAi agent with the target miRNA and the subsequent downregulation
of the miRNA.
[0215] In one embodiment, the RNAi agent targets an miRNA normally
expressed in liver tissue, and in another embodiment, the human is
suffering from a disorder characterized by decreased expression of
the miRNA in the liver. Administration of the RNAi agent to the
subject, or to a cell of the liver, at least partially rescues the
function of the downregulated miRNA.
[0216] In one embodiment, the RNAi agent targets an RNA that is the
product of a gene from a pathogenic organism. For example, a
hepatocyte infected with any of a number of hepatitis viruses, e.g.
hepatitis A, B or C, will produce various RNAs and proteins from
the viral genome that relate to viral replication.
[0217] In one embodiment, the RNAi agent targets a gene related to
the formation of fibrotic lesions in the liver, e.g. a gene related
to the formation of the extracellular matrix, e.g. a collagen
gene.
[0218] In one embodiment, the RNAi agent targets a gene related to
the development and progression of cancer, e.g. of liver cancer,
e.g. of hepatocellular carcinoma. For example, a gene essential for
the proliferation of cells may be targeted, for example, without
limitation, a gene involved in the formation of the mitotic
spindle, or a gene that inhibits the apoptosis of cancer cells,
e.g. bcl-2.
[0219] Finally, the present invention also provides the use of an
RNAi agent according to the invention for the preparation of a
pharmaceutical composition for curative, preventive or vaccine
treatment of mammals. Preferably, such compositions are intended
for the treatment of the human or animal body. "Treatment" as used
herein refers to prophylaxis and therapy. It concerns both the
treatment of humans and animals. A "therapeutically effective
amount of a peptide or a composition" is a dose sufficient for the
alleviation of one or more symptoms normally associated with the
disease desired to be treated. A method according to the invention
is preferentially intended for the treatment of the diseases listed
above.
[0220] Route of Delivery
[0221] The RNAi agents described herein can be administered by
various routes of delivery, e.g., by oral, pulmonary, intravenous,
topical, rectal, anal, or vaginal, delivery, e.g. as described in
International Application Serial No. PCT/US2004/11829, filed Apr.
16, 2004. The contents of this reference are incorporated herein in
their entirety.
[0222] Dosage
[0223] In one aspect, the invention features a method of
administering an RNAi agent to a subject (e.g., a human subject).
The method includes administering a unit dose of the RNAi agent
that targets an RNA, e.g., an mRNA, in the subject (e.g., an
endogenous or pathogen target RNA). In one embodiment, the unit
dose is less than 1.4 mg per kg of bodyweight, or less than 10, 5,
2, 1, 0.5, 0.1, 0.05, 0.01, 0.005, 0.001, 0.0005, 0.0001, 0.00005
or 0.00001 mg per kg of bodyweight, and less than 200 nmole of RNAi
agent (e.g. about 4.4.times.10.sup.16 copies) per kg of bodyweight,
or less than 1500, 750, 300, 150, 75, 15, 7.5, 1.5, 0.75, 0.15,
0.075, 0.015, 0.0075, 0.0015, 0.00075, 0.00015 nmole of RNAi agent
per kg of bodyweight.
[0224] The defined amount can be an amount effective to treat or
prevent a disease or disorder, e.g., a disease or disorder
associated with the target RNA, such as an RNA present in the
liver. The unit dose, for example, can be administered by injection
(e.g., intravenous or intramuscular), an inhaled dose, or a topical
application. Particularly preferred dosages are less than 2, 1, or
0.1 mg/kg of body weight.
[0225] In a preferred embodiment, the unit dose is administered
less frequently than once a day, e.g., less than every 2, 4, 8 or
30 days. In another embodiment, the unit dose is not administered
with a frequency (e.g., not a regular frequency). For example, the
unit dose may be administered a single time.
[0226] In one embodiment, the effective dose is administered with
other traditional therapeutic modalities. In one embodiment, the
subject has a viral infection and the modality is an antiviral
agent other than an RNAi agent. In another embodiment, the subject
has atherosclerosis and the effective dose of an RNAi agent is
administered in combination with, e.g., after surgical
intervention, e.g., angioplasty.
[0227] In one embodiment, a subject is administered an initial dose
and one or more maintenance doses of an RNAi agent, or a precursor,
e.g., a larger RNAi agent which can be processed into an RNAi
agent. The maintenance dose or doses are generally lower than the
initial dose, e.g., one-half less of the initial dose. A
maintenance regimen can include treating the subject with a dose or
doses ranging from 0.01 .mu.g to 1.4 mg/kg of body weight per day,
e.g., 10, 1, 0.1, 0.01, 0.001, or 0.00001 mg per kg of bodyweight
per day. The maintenance doses are preferably administered no more
than once every 5, 10, or 30 days. Further, the treatment regimen
may last for a period of time, which will vary depending upon the
nature of the particular disease, its severity and the overall
condition of the patient. In preferred embodiments the dosage may
be delivered no more than once per day, e.g., no more than once per
24, 36, 48, or more hours, e.g., no more than once for every 5 or 8
days. Following treatment, the patient can be monitored for changes
in his condition and for alleviation of the symptoms of the disease
state. The dosage of the compound may either be increased in the
event the patient does not respond significantly to current dosage
levels, or the dose may be decreased if an alleviation of the
symptoms of the disease state is observed, if the disease state has
been ablated, or if undesired side-effects are observed.
[0228] The effective dose can be administered in a single dose or
in two or more doses, as desired or considered appropriate under
the specific circumstances. If desired to facilitate repeated or
frequent infusions, implantation of a delivery device, e.g., a
pump, semi-permanent stent (e.g., intravenous, intraperitoneal,
intracisternal or intracapsular), or reservoir may be
advisable.
[0229] In one embodiment, the RNAi agent pharmaceutical composition
includes a plurality of RNAi agent species. In another embodiment,
the RNAi agent species has sequences that are non-overlapping and
non-adjacent to another species with respect to a naturally
occurring target sequence. In another embodiment, the plurality of
RNAi agent species is specific for different naturally occurring
target genes. In another embodiment, the RNAi agent is allele
specific.
[0230] In some cases, a patient is treated with an RNAi agent in
conjunction with other therapeutic modalities. For example, a
patient being treated for a liver disease, e.g., early stage
hepatocellular carcinoma, can be administered an RNAi agent
specific for a target gene known to enhance the progression of the
disease in conjunction with a drug known to inhibit activity of the
target gene product. For example, a patient who has early stage
hepatocellular carcinoma can be treated with an RNAi agent that
targets, for example, bcl-2, or a gene involved in DNA adduct
repair, in conjunction with the small molecule cisplatin, which is
known to form DNA adducts, primarily intrastrand crosslink adducts
(See Siddikh, Oncogene. 2003, 22:7265).
[0231] Following successful treatment, it may be desirable to have
the patient undergo maintenance therapy to prevent the recurrence
of the disease state, wherein the compound of the invention is
administered in maintenance doses, ranging from 0.01 .mu.g to 100 g
per kg of body weight (see U.S. Pat. No. 6,107,094).
[0232] The concentration of the RNAi agent composition is an amount
sufficient to be effective in treating or preventing a disorder or
to regulate a physiological condition in humans. The concentration
or amount of RNAi agent administered will depend on the parameters
determined for the agent and the method of administration, e.g.
oral, nasal, buccal, pulmonary, intravenous, or rectal delivery.
For example, nasal formulations tend to require much lower
concentrations of some ingredients in order to avoid irritation or
burning of the nasal passages. It is sometimes desirable to dilute
an oral formulation up to 10-100 times in order to provide a
suitable nasal formulation.
[0233] Certain factors may influence the dosage required to
effectively treat a subject, including but not limited to the
severity of the disease or disorder, previous treatments, the
general health and/or age of the subject, and other diseases
present. Moreover, treatment of a subject with a therapeutically
effective amount of an RNAi agent, e.g., a double-stranded RNAi
agent, or precursor thereof) can include a single treatment or,
preferably, can include a series of treatments. It will also be
appreciated that the effective dosage of an RNAi agent used for
treatment may increase or decrease over the course of a particular
treatment. Changes in dosage may result and become apparent from
the results of diagnostic assays as described herein. For example,
the subject can be monitored after administering an RNAi agent
composition. Based on information from the monitoring, an
additional amount of the RNAi agent composition can be
administered.
[0234] Dosing is dependent on severity and responsiveness of the
disease condition to be treated, with the course of treatment
lasting from several days to several months, or until a cure is
effected or a diminution of disease state is achieved. Optimal
dosing schedules can be calculated from measurements of drug
accumulation in the body of the patient. Persons of ordinary skill
can easily determine optimum dosages, dosing methodologies and
repetition rates. Optimum dosages may vary depending on the
relative potency of individual compounds, and can generally be
estimated based on EC.sub.50 found to be effective in in vitro and
in vivo animal models. In some embodiments, the animal models
include transgenic animals that express a human gene, e.g. a gene
that produces a target RNA. The transgenic animal can be deficient
for the corresponding endogenous RNA. In another embodiment, the
composition for testing includes an RNAi agent that is
complementary, at least in an internal region, to a sequence that
is conserved between the target RNA in the animal model and the
target RNA in a human.
[0235] In one aspect, the invention features a method that
includes: administering a first amount of a composition that
comprises an RNAi agent, e.g., a double-stranded RNAi agent or
precursor thereof) to a subject, wherein the RNAi agent is
substantially complementary to a target nucleic acid; evaluating an
activity associated with a protein encoded by the target nucleic
acid; wherein the evaluation is used to determine if a second
amount should be administered. In a preferred embodiment the method
includes administering a second amount of the composition, wherein
the timing of administration or dosage of the second amount is a
function of the evaluating. The method can include other features
described herein.
[0236] In another aspect, the invention features a method of
administering a source of an RNAi agent to a subject. The method
includes administering or implanting a source of an RNAi agent. In
one embodiment, the source releases the RNAi agent over time, e.g.
the source is a controlled or a slow release source, e.g., a
microparticle that gradually releases the RNAi agent. In another
embodiment, the source is a pump, e.g., a pump that includes a
sensor or a pump that can release one or more unit doses.
[0237] In one aspect, the invention features a pharmaceutical
composition that includes an RNAi agent, including a nucleotide
sequence sufficiently complementary to a target RNA to allow duplex
formation with a target nucleic acid. The target RNA can be a
transcript of an endogenous human gene. In one embodiment, the RNAi
agent (a) is about 5 to about 100 nucleobases long, e.g., about 8
to about 75, e.g., about 8 to about 50 nucleotides long, e.g.,
about 15 to about 30 nucleotides long, e.g., 15, 16, 17, 18, 19,
20, 21, 22, 23, 24, or 25 nucleotides; and (b) is complementary to
an endogenous target RNA In one embodiment, the pharmaceutical
composition can be an emulsion, microemulsion, cream, jelly, or
liposome.
[0238] In certain other aspects, the invention provides kits that
include a suitable container containing a pharmaceutical
formulation of an RNAi agent or a precursor of an RNAi agent). In
certain embodiments the individual components of the pharmaceutical
formulation may be provided in one container. Alternatively, it may
be desirable to provide the components of the pharmaceutical
formulation separately in two or more containers, e.g., one
container for a preparation comprising one strand of the RNAi
agent, and at least another for the second strand. The kit may be
packaged in a number of different configurations such as one or
more containers in a single box. The different components can be
combined, e.g., according to instructions provided with the kit.
The components can be combined according to a method described
herein, e.g., to prepare and administer a pharmaceutical
composition. The kit can also include a delivery device.
[0239] In another aspect, the invention features a device, e.g., an
implantable device, wherein the device can dispense or administer a
composition that includes an RNAi agent, or a precursor, e.g., a
larger RNAi agent which can be processed into an RNAi agent. The
RNAi agent can inhibit expression of an endogenous transcript. In
one embodiment, the device is coated with the composition. In
another embodiment the RNAi agent is disposed within the device. In
another embodiment, the device includes a mechanism to dispense a
unit dose of the composition. In other embodiments the device
releases the composition continuously, e.g., by diffusion.
Exemplary devices include stents, catheters, pumps, artificial
organs or organ components (e.g., artificial heart, a heart valve,
etc.), and sutures.
[0240] Cells Comprising an RNAi Agent of the Invention
[0241] The invention further concerns a cell comprising an RNAi
agent of the invention. Preferred embodiments of the instant cell
are as provided for other inventive aspects above. According to the
invention, "cells" include prokaryotic cells and eukaryotic cells,
yeast cells, plant cells, human or animal cells, in particular
mammalian cells. In a preferred embodiment, the cell is a
hepatocyte,. In particular, cancer cells should be mentioned. In
preferred embodiments, the cell will be a cell expressing the
asialoglyprotein receptor, such as a hepatocyte, preferably of
mammalian, and more preferably of human, origin.
[0242] Remarks
[0243] These and other embodiments are disclosed or are obvious
from and encompassed by the description and examples of the present
invention. Further literature concerning any one of the methods,
uses and compounds to be employed in accordance with the present
invention may be retrieved from public libraries, using for example
electronic devices. For example the public database "Medline" may
be utilized which is available on Internet, e.g. under
http://www.ncbi.nlm.nih.gov/PubMed/medline.html. Further databases
and addresses, such as http://www.ncbi.nlm.nih.gov,
http://www.infobiogen.fr, http://www.fmi.ch/biology/researchi3
tools.html, http://www.tigr.org, are known to the person skilled in
the art and can also be obtained using, e.g., http://www.lycos.com.
An overview of patent information in biotechnology and a survey of
relevant sources of patent information useful for retrospective
searching and for current awareness is given in Berks, TIBTECH 12
(1994), 352-364.
[0244] The methods, compositions and uses of the invention can be
applied in the treatment of all kinds of diseases the treatment
and/or diagnostic of which is related to or dependent on the
transfer of nucleic acids in cells. The compositions, and uses of
the present invention may be desirably employed in humans, although
animal treatment is also encompassed by the uses described
herein.
[0245] The invention has been described in an illustrative manner,
and it is to be understood that the terminology which has been used
is intended to be in the nature of words of description rather than
of limitation. Obviously, many modifications and variations of the
present invention are possible in light of the above teachings. It
is therefore to be understood that within the scope of the appended
claims, the invention may be practiced different from what is
specifically described herein.
[0246] The disclosure of all patents, publications, published
patent applications, and database entries cited in the present
application are hereby incorporated by reference in their entirety
to the same extent as if each such individual patent, publication
and database entry were specifically and individually indicated to
be incorporated by reference and were set forth in its entirety
herein.
EXAMPLES
1. Materials
[0247] Where the source of a reagent is not specifically given
herein, such reagent may be obtained from any supplier of reagents
for molecular biology at a quality/purity standard for application
in molecular biology.
[0248] SYNTHESIS OF
1-O-{4-[(2--CYANOETHOXY)-N,N-DIISOPROPYLAMINO-PHOSPHANYLOXY]-BUTYL}-6-O-(-
4-METHOXYTRIPHENYLMETHYL)-2,3,4-TRI-O-ACETYL-B-D-GALACTOPYRANOSIDE
(9)
[0249] The synthesis of compound 9 is illustrated in FIG. 6. 20 g
(51.24 mmol) of .beta.-D-galactosepentaacetate 1 was dissolved in
150 ml THF and 6.7 ml (61.49 mmol) of benzylamine was added with a
dropping funnel. The reaction was stirred for 18 h at room
temperature to give 2,3,4,6-tetra-O-acetyl-.beta.-D-galactopyranose
2.
[0250] Product 2 was dissolved in 50 ml (240 mmol)
trichloacetonitrile and cooled down to -20.degree. C. Within 15 min
3.56 ml (23.96 mmol) of 1,8-Diazabicyclo[5.4.0]-undec-7-ene were
added using a dropping funnel. After 1.5 h synthesis of
2,3,4,6-tetra-O-acetyl-D-galactopyranosyl-trichloracetimidate 3 was
completed and the solvent was removed under reduced pressure. The
residue was chromatographed over Kieselge160 using
cyclohexane/acetic acid ethyl ester 4:1 and product 3 was obtained
in 71.5% yield.
[0251] 19 g (38.38 mmol) of product 3 were dissolved in 150 ml
CH.sub.2Cl.sub.2 and 13.34 ml (57.57 mmol)
4-(tent-butyldimethylsilyl)-oxy-1-butanole was added. 2.47 g (9.59
mmol) Silver-trifluormethansulfonate in 0.5 ml Toluol was dissolved
in a flask and cooled down to -78.degree. C. Product 3 was added
over a dropping funnel within 10 min and reaction was stirred for
20 h. Afterwards 0.3 eq. triethylamine were added and the mixture
was diluted with 50 ml CH.sub.2Cl.sub.2 for extraction with 0.2 M
HCl and sodium hydrogen carbonate. The solution was dried over
Na.sub.2SO.sub.4 and solvent was removed under reduced pressure.
1--O-(4-tert-butyl-dimethyl
silyloxybutyl)-2,3,4,6-tetra-O-acetyl-.beta.-D-galactopyranoside 4
was purified over Kieselge160 (cyclohexane/acetic acid ethyl ester
6:1) in 77.9% yield.
[0252] To obtain
1-O-(4-tert-butyl-dimethylsilyloxy)-.beta.-D-galactopyranoside 5
product 4 (15.28 g 29.29 mmol) was dissolved in 30 ml methanol and
2 ml sodium methylate (25% in methanol) were added at room
temperature. The mixture was stirred for 3 h and an equal amount of
methanol was added as well as portions of an anionic exchange
material Amberlit IR-120 to generate a pH around 7.0. The Amberlit
was removed by filtration, the solution was dried with
Na.sub.2SO.sub.4 and the solvent was removed under reduced
pressure.
[0253] For protecting C6-OH by a monomethoxytrityl group (MMT)
product 5 was dissolved in 30 ml pyridine and converted with 23.5 g
(59 mmol) 4-Methoxytrityl-chloromethane into the corresponding
1-O-[4-tert-butyl-dimethylsilyloxybutyl]-6-O-(4-methoxytriphenylmethyl)-.-
beta.-D-galactopyranoside 6 (MacKellar et al., Nucleic Acids Res
1992, 20:3411).
[0254] Product 6 (theoretically 29.29 mmol) was then peracetylated
without any purification using 33 ml (351.5 mmol) acetic anhydride
(99%) in additionally 15 ml pyridine. After 16 h the synthesis of
von
1-O-[4-tert-butyl-dimethylsilyloxybutyl]-6-O-(4-methoxytriphenylmethyl)-2-
,3,4-tri-O-acetyl-.beta.-D-galactopyranoside 7 was completed and
solvent was removed under reduced pressure. The residue was
chromatographed over Kieselge160 using cyclohexane/acetic acid
ethyl ester 10:1 in order to give product 7 in 39.6% yield.
[0255] Product 7 was dissolved in 15 ml THF and 4 ml (22.25 mmol)
of tetrabutylammoniumfluoride (1M in THF) were added using a
dropping funnel (1 drop/sec). 24 h later the separation of the
protecting group was completed
1-O-[4hydroxybutyl]-6-O-(4-methoxytriphenylmethyl)-2,3,4-tri-O--
acetyl-.beta.-D-galacto-pyranoside 8 was obtained in 70.2%
yield.
[0256] .sup.1H-NMR (300 MHz), CDCl.sub.3): 4.90-5.00 (d, J1/2=6.,77
Hz, 1H, H-1.beta.).
[0257] .sup.13C-NMR(75 MHz), CDCl.sub.3): .delta.=171.1-169.9 (3C,
O.dbd.C--CH.sub.3); 158.6 (p-Ar); 144.8 (2C, C.sup.MMT-3); 136.0
(C.sup.MMT-2); 130.9 (2C, o-Ar); 128.3 (4C, o'-Ar); 127.7
(4C,m'-Ar); 126.9 (4C, p'-Ar); 113.1 (2C, m-Ar); 103.1 (C-1.beta.);
86.4 (C .sup.MMT-1); 72.8 (C-2); 72.5 (C-3); 72.0 (C-4); 70.3
(C-5); 69.3 (C-1'); 68.0 (C-4'); 62.3 (C-6); 55.1 (O--CH.sub.3);
26.8 (C-2'); 26.4 (C-3'); 22.6 (3C, O.dbd.C--CH.sub.3).
[0258] In order to synthesize
OF1-O-{4-[(2-cyanoethoxy)-N,N-diisopropylamino-phosphanyl
oxy]-butyl}-6-O-(4-methoxytriphenylmethyl)-2,3,4-tri-O-acetyl-.beta.-D-ga-
lactopyranoside 9 product 8 (3.5 g; 5.38 mmol) was dissolved in 20
ml acetonitrile and filled in a flask that previuos was
equilibrated with argon using a needle. Subsequently 1.12 ml (6.45
mmol) N-ethyldiisopropylamine, 2.65 ml (8.07 mmol)
2-cyanoethyl-N,N,N,N-tetraisopropylphosphane and 11.8 ml (5.92
mmol) S-ethylthiotetrazole (0.5 M) were added using a needle. After
1.5 h conversion into the phosphoramidite was completed and the
mixture was extracted with a sodium chloride solution and dried
over Na.sub.2SO.sub.4. The solvent was removed under reduced
pressure and the residue was chromatographed (cyclohexane/acetic
acid ethyl ester 3:1) to give product 9 in 74.3% yield as a white
crystalline solid.
[0259] Synthesis of Sirnas
[0260] Single-stranded RNAs were produced by solid phase synthesis
on a scale of 1 .mu.mole using an Expedite 8909 synthesizer
(Applied Biosystems, Applera Deutschland GmbH, Darmstadt, Germany)
and controlled pore glass (CPG, 500 .ANG., Proligo Biochemie GmbH,
Hamburg, Germany) as solid support. RNA and RNA containing
2'-O-methyl nucleotides were generated by solid phase synthesis
employing the corresponding phosphoramidites and 2'-O-methyl
phosphoramidites, respectively (Proligo Biochemie GmbH, Hamburg,
Germany). These building blocks were incorporated at selected sites
within the sequence of the oligoribonucleotide chain using standard
nucleoside phosphoramidite chemistry such as described in Current
protocols in nucleic acid chemistry, Beaucage, S. L. et al.
(Edrs.), John Wiley & Sons, Inc., New York, N.Y., USA.
Phosphorothioate linkages were introduced by replacement of the
iodine oxidizer solution with a solution of the Beaucage reagent
(Chruachem Ltd, Glasgow, UK) in acetonitrile (1%). Further
ancillary reagents were obtained from Mallinckrodt Baker
(Griesheim, Germany).
[0261] Galactose conjugated siRNAs were synthesized using the same
protocols as above with additional coupling of a symmetrical
branching CED phosphoramidite (SB, ChemGenes) and the synthesized
galactose amidite 9 (FIG. 7). In case of the SBTEGGAL modification
a tetraethylene glycol (TEG, ChemGenes) was introduced between the
SB linkage and the galactose moiety.
[0262] RNA synthesis of the Chol-siRNAs started from a controlled
pore glass solid support carrying a cholesterol-aminocaproic
acid-pyrrolidine linker, the synthesis of which is described
elsewhere (Soutschek et al., Nature 2004, 432:173; US patent
application, publication number 20060105976). To generate
fluorescently labeled antisense strands an additional coupling of
an Indodicarbocyanine3-1-o --CED-phosphoreamidite (Cy3, ChemGenes)
at the 5' end of the antisense strand was performed.
[0263] Deprotection and purification of the crude
oligoribonucleotides by anion exchange HPLC were carried out
according to established procedures. Yields and concentrations were
determined by UV absorption of a solution of the respective RNA at
a wavelength of 260 nm using a spectral photometer (DU 640B,
Beckman Coulter GmbH, UnterschleiBheim, Germany), and products
characterized by ES mass spectrometry. Double stranded RNA was
generated by mixing an equimolar solution of complementary strands
in annealing buffer (20 mM sodium phosphate, pH 6.8; 100 mM sodium
chloride), heated in a water bath at 85-90.degree. C. for 3 minutes
and cooled to room temperature over a period of 3-4 hours. The
annealed RNA solution was diluted to a concentration of 50 .mu.mole
double stranded RNA/1 and stored at -20.degree. C. until use.
[0264] The siRNAs used in this study consisted of a 21-nucleotide
sense strand and a 23-nucleotide antisense strand resulting in a
two-nucleotide overhang at the 3' end of the antisense strand. ApoB
siRNA (ORF position 10049-10071): sense
5'-GUCAUCACACUGAAUACCAA*U-3'(SEQ ID NO: 1); antisense
5'-AUUGGUAUUAGUGUGUGAc* a*C-3'(SEQ ID NO: 2); bc12 siRNA: sense
5'-GGCCUUCUUUGAGUUCGGUGG-3 '(SEQ ID NO: 3); anti sense
5'-CCACCGAACUCAAAGAAGGCcaC-3'(SEQ ID NO: 4); gfp siRNA: sense
5'-CCACAUGAAGCA GCACGACUU-3'(SEQ ID NO: 5); antisense
5'-AAGUCGUGCUGCUUCAUGUG guC-3'(SEQ ID NO: 6). The lower-case letter
represent 2'-O-methyl-modified nucleotides; asterisks represent
phosphorothioate linkages.
[0265] To generate siRNAs from RNA single strands, equimolar
amounts of complementary sense and antisense strands were mixed and
annealed and siRNAs were further characterized by gel
electrophoresis.
[0266] In Vitro Activity and Silencing Experiments
[0267] To determine the in vitro activity of siRNAs, HuH7 cells
were transfected with siRNAs using oligofectamine (Invitrogen) and
siRNA concentrations ranging from 0.1 nM to 100 nM. ApoB protein
content was determined from cell culture supernatant by a sandwhich
ELISA capturing apoB with a polyclonal goat anti human apoB
antibody (Chemicon International). ApoB detection was performed 48
h after transfection with a horseraddish peroxidase-conjugated goat
anti human apoB-100 polyclonal antibody (Academy Bio-Medical
Company). The remaining apoB content was calculated as the ratio of
apoB protein in the supernatant of the cells treated with
apoB-specific siRNA to the apoB protein in the supernatant of cells
treated with unrelated control siRNAs. The QuantiGene assay
(Genospectra) was used to quantify the reduction of apoB mRNA after
siRNA treatment. Lysates from the cells were directly used for apoB
and gapdh quantification, and the ratio of apoB and gapdh mRNA was
calculated and expressed as a group average relative to cells
treated with unrelated control siRNAs. Specific probes for
detection of apoB and gapdh mRNA levels were designed to the
following regions of the mRNA ORF: probe set apoB 8374-8776; probe
set gapdh 252-472.
[0268] The complete panel of siRNAs was also evaluated for the
ability to mediate posttranscriptional silencing of the apoB gene
expression without using a transfection reagent. For these
experiments cells were incubated with the same siRNAs used in the
transfection experiments in concentrations at 10 5 .mu.M and 1
.mu.M siRNA. Cells were seeded in serum free media and the siRNAs
were added. Four hours after siRNA donation fetal calf serum was
added and 48 h after siRNA administration protein and mRNA contents
were determined as described above. The same experiments was
performed with HuH7 cells cultured in 5 mM CaCl.sub.2 to activate
the asialoglycoprotein receptor. After washing and seeding of the
cells the siRNAs were added in the same concentrations as mentioned
above.
[0269] For competition experiments HuH7 cells were incubated with 1
mM N-acetylgalactosamine at 37.degree. C. in serum free media and
siRNAs were added after 30 min in concentration at 10 .mu.M, 5
.mu.M and 1 .mu.M. 48 h after siRNA administration protein and mRNA
contents were determined as outlined above.
[0270] Flourescence Microscopy and Uptake Studies
[0271] To determine an uptake of the galactose conjugated siRNAs
into the cytoplasm the sense strands were annealed with a Cy3
(Indodicarbocyanine 3) labeled antisense strand. After an
incubation time of 16 h and a siRNAs concentration of 10 .mu.M the
cell culture media was removed and cells were washed twice with PBS
to eliminate siRNAs that were not taken up by the cells and 100
.mu.l/well of normal media was added. Accordingly 10 .mu.l/well of
a 0.1 mg/ml stock solution of
4',6-Diamidino-2-phenylindoldihydrochloride (Sigma) were added and
the cells were incubated for 30 min at 37.degree. C. After washing
the cells twice with PBS and adding fresh media the fluorenscence
exposures were performed with an Olympus IX50 microscope and a
monochrome camera (7.0 monochrome IR, Diagnostic Instruments) and
pictures were analyzed with the MetaView Imaging software (Visitron
Systems). To visualize the Cy3 fluorescence a NIB (Ex.sub.max
547/Em.sub.max 563 nm) filter was used and the exposure of the DAPI
fluorescence was performed with a NB filter (Ex.sub.max 365 nm).
Completing an overlay of both fluorescence exposures were created
using the MetaView Imaging software.
[0272] In this study we describe the synthesis of galactose
conjugated siRNAs. Using this approach it was undertaken to
generate uptake via receptor mediated processes in liver cells as
shown from Biessen and colleagues with galactose modified molecules
(Biessen et al., Biochem. J. 1999, 340(Pt 3):783; Biessen et al.,
Methods Enzymol. 2000, 314:324; Rensen et al., J. Biol. Chem. 2001,
276:37577). Glycoconjugation of siRNAs with branched structures
comprising galactose was selected to target the asialoglycoprotein
receptor. A phosphoramidite was generated from
.beta.-D-Galactosepentaacetate as outlined in FIG. 6 and two
different 5'-modified siRNAs were synthesized on solid phase.
[0273] Two linkage structures broadened the chemical space probed
by this investigation. First a symmetrical branching linker (SB)
was coupled to the 5'-end of the sense strand during solid phase
synthesis followed by coupling of the galactose phosphoramidite 9
to generate the SBGAL conjugate (FIG. 7). The second approach used
an additionally inserted tetraethylene glycol linkage (TEG) between
the symmetrical branching linker and the galactose residues to
synthesize the SBTEGGAL conjugate. This procedure aimed for an
increased distance (.about.16 .ANG.) between the negatively charged
siRNA and the sugar moiety, because it was already shown that an
upper gap advance the binding and internalisation via the
asialoglycoprotein receptor (Biessen et al., Biochem. J 1994,
302(Pt 1):283).
[0274] In vitro sudies with modified siRNAs using a transfection
agent
[0275] The ability of the above described conjugates to mediate
posttranscriptional silencing of the apoB gene expression was
demonstrated by classic transfection experiments using
oligofectamine (FIG. 1). Silencing of the apoB mRNA would be
expected to result in a corresponding reduction in apoB 100 protein
levels. The apoB 100 protein and mRNA levels were measured by
enzyme-linked immunosorbent assay (ELISA) and b-DNA in HuH7
hepatocarcinoma cells after transfection at siRNA concentrations
ranging from 100 nM to 0.1 nM. The data are presented as mean
values with corresponding standard diviation of three assays in
triplicates normalized to the average level of unrelated siRNAs
(b442, b442SBGAL and gfp3'Chol). Both galactose conjugated siRNAs
SBGAL and SBTEGGAL are able to reduce the apoB 100 protein and mRNA
content in a dose dependant manner comparable to that of the
unmodified apoB sequence. As shown in FIG. 1a and b, cells treated
with 100 nM SBGAL and SBTEGGAL modified siRNAs showed statistically
significant reductions (mean.+-.s.d.; protein: SBGAL 87.+-.5%;
SBTEGGAL 73.+-.3% and mRNA: SBGAL 79.+-.9%; SBTEGGAL 71.+-.7%) in
apoB 100 protein and mRNA levels as compared with the mean of the
unspecific controls (P*<0.001). The 3' Chol modified siRNA used
as a positive control in all experiments (Soutschek et al., Nature
2004, 432:173) showed a lower silencing effect at the same siRNA
concentration compared to that of the suger conjugated and
unmodified siRNAs (mean.+-.s.d.; protein: 52% .+-.14%; mRNA:
69.+-.8%). In summary, the 5'-modification of the sense strand with
branched galactose structures did not affect the in vitro activity
of these compounds to mediate a posttranscriptional silencing of
the apoB gene expression.
[0276] Delivery Experiments in the Absence of a Transfection
Agent
[0277] Glycoconjugation of the siRNA with branched galactose
structures was selected to target the asialoglycoprotein receptor
(ASGPR). To demonstrate the ability of galactose conjugated siRNAs
SBGAL and SBTEGGAL to silence apoB expression in vitro without
using transfection agents HuH7 cells were incubated with these
siRNAs in concentrations ranging from 10 .mu.M to 1 and protein and
mRNA levels were determined using ELISA and b-DNA (FIG. 2a and b).
The results presented in FIG. 2a and b show that incubation with
galactose modified siRNAs resulted in a dose-dependent significant
decrease of apoB 100 protein and mRNA content (P*<0.005). Using
a dose of 10 .mu.M SBGAL conjugated siRNA the apoB 100 protein was
reduced to 56.+-.14% and the mRNA content decreased to 68.+-.5%.
The SBTEGGAL conjugate also caused a reduction of the protein level
(mean.+-.s.d.; 58.+-.7%) and mRNA content (60.+-.14%) compared to
unrelated siRNAs. Furthermore the 3' Chol modified siRNA permitted
a decrease of apoB protein and mRNA equal to that of the suger
conjugated siRNAs at a concentration of 10 .mu.M siRNA
(mean.+-.s.d.; protein: 54.+-.6%; mRNA: 49.+-.15%). In contrast
cells treated with the unmodified apoB siRNA showed no significant
reduction in the apoB 100 protein or mRNA levels, because as
expected due to their negative charge and high molecular weight
unmodified siRNAs are not able to cross cellular membranes.
Ultimately, a dose-dependent reduction of apoB protein and mRNA
contents could be demonstrated in the absence of any transfection
reagent using galactose modified siRNAs, suggesting receptor
mediated uptake.
[0278] Improved Silencing Effects for Galactose Conjugated Sirnas
Upon Receptor Activation
[0279] The galactose conjugated siRNAs were synthesized to target
the asialoglycoprotein receptor (ASGPR), which is expressed on the
cell surface of hepatocytes. The ASGPR is capable of internalizing
galactose terminated molecules (Biessen et al., Methods Enzymol
2000, 314:324; Biessen et al., Biochem J 1999, 340(Pt 3):783;
Biessen et al., Biochem J 1994, 302(Pt 1):283; Rensen et al., J
Biol Chem 2001, 276:37577; Hangeland et al., Bioconj Chem 1995,
6:695; Duff et al., Methods Enzymol 2000, 313:297). These receptors
belong to the family of C-type lectins, and their functionality is
calcium dependent (Van Lenten and Ashwell, J Biol Chem 1972,
247:4633; Drickamer, J Biol. Chem 1988, 263:9557). To further
confirm the mediation of uptake via the receptor, HUH7 cells were
cultured in a growth medium containing 5 mM CaCl.sub.2 in order to
activate the receptor. In contrast the direct incubation
experiments with the siRNAs were performed after removing the
growth medium and washing the cells with PBS. The same procedure as
for the incubation experiments without receptor activation was
performed at siRNA concentrations ranging from 10 .mu.M to 1 .mu.M.
Protein and mRNA levels were determined using ELISA and the b-DNA
assay, and data evaluated as means with standard deviation relative
to unrelated siRNAs (b442, b442SBGAL, b442SBTEGGAL and gfp3' Chol).
As shown in FIG. 3a and b, receptor activation with calcium
chloride resulted in significantly improved and dose-dependent
silencing effects by the galactose conjugated siRNAs, whereas the
activity of the 3' Chol modified siRNA remained unaffected
(P*<0,001). The SBGAL conjugated siRNA decreased apoB mRNA
content by about 70.+-.7% at a concentration of 10 .mu.M siRNA. At
the same concentration the siRNA containing an additional TEG
linkage (SBTEGGAL) reduced mRNA content by 90.+-.2%. Silencing of
the mRNA resulted in corresponding decreases in protein levels
(36.+-.10%; 10.+-.6%). Culturing the cells in calcium chloride had
no effect on gene silencing by the unmodified apoB siRNA; as
expected, no silencing was observed. Furthermore the unrelated
siRNAs having the same galactose modifications as the apoB siRNAs
also were not able to decrease apoB protein and mRNA contents.
Thus, an unspecific effect of the galactose modification itself is
excluded. The results presented herein additionally support a
receptor mediated uptake for the galactose conjugated siRNAs SBGAL
and SBTEGGAL.
[0280] Galactose Conjugated Sirnas are Localized in the
Cytoplasm
[0281] Due to the ability of the galactose modified siRNAs to
silence the apoB gene expression it can be assumed that these
siRNAs are able to cross the cellular membrane and enter the
cytoplasm of the target cells without using a transfection agent.
To determine the uptake into the cell fluorescently labeled siRNAs
were used to visualize these siRNAs in intracellular compartments.
Therefore cells were grown in the absence or presence of 5 mM
calcium chloride to activate the asialoglycoprotein receptor and
fluorescently labeled siRNAs were added at a concentration of 10
.mu.M. 16 h after siRNA administration exposures were generated
using fluorescence microscopy (FIG. 5). Internalisation of the
modified apoB siRNAs was determined by
4',6-Diamidino-2-phenylindoldihydrochloride staining of the nucleus
and fluorescence was localized around the nucleus (not shown).
Cells grown in normal cell culture media and incubated with
galactose modified siRNAs showed a minimal fluorescence within the
cytoplasm (FIG. 5, left panel), whereas culturing the cells in 5 mM
calcium chloride in order to activate the asialoglycoprotein
receptor significantly enhance intracellular fluorescence (FIG. 5,
right panel). In contrast the 3'-Cholesterol modified siRNA
remained unaffected and these cells showed an equal distribution of
the siRNA within the cytoplasm with or without receptor activation.
Uptake of the unmodified apoB siRNA as well remained unaffected and
no fluorescence could be detected within the cells. As expected,
culturing the cells in 5 mM calcium chloride had no effect on the
uptake of the unmodified apoB sequence. Hence, it was further
demonstrated that the galactose conjugated siRNAs are selectively
taken up by parenchymal liver cells upon receptor activation with
calcium chloride.
[0282] Competition of Galactose Conjugated Sirnas with Other
Ligands of the Asgpr
[0283] To investigate whether the galactose conjugated siRNAs are
specifically taken up by the asialoglycoprotein receptor,
competition studies with N-acetylgalactosamine were performed.
GalNAc is known to possess a 40 to 50-fold higher binding affinity
for the ASGPR as compared to galactose (Rensen et al., J. Biol.
Chem. 2001, 276:37577). Cells were seeded and preincubated for 30
min with 1 mM GalNAc and than the siRNAs were added in
concentrations of 10 .mu.M, 5 .mu.M and 1 .mu.M. As shown in FIG. 4
a and b, preincubation with GalNAc resulted in an almost complete
inhibition of the silencing effect caused by the galactose
conjugated siRNAs SBGAL and SBTEGGAL. No significant reductions in
apoB protein and mRNA contents could be observed (protein content
10 .mu.M SBGAL siRNA 99.+-.9%; SBTEGGAL 96.+-.6% and mRNA content
SBGAL 75.+-.3%; SBTEGGAL 84.+-.10%). In contrast the RNA
interference effect and resulting reduction in apoB protein and
mRNA levels caused by the 3'-Cholesterol modified siRNA remained
unaffected. These results further confirm that the galactose
containing siRNAs are selectively taken up by the
asialoglycoprotein receptor and that this uptake can be competed
out by an excess of N-acetylgalactosamine, whereas the uptake of
3'-Chol conjugated siRNAs seems to occur via another mechanism.
Sequence CWU 1
1
6121RNAArtificial Sequencesource/note="Description of Artificial
Sequence Synthetic
oligonucleotide"misc_feature(20)..(21)Phosphorothioate linkage
1gucaucacac ugaauaccaa u 21221RNAArtificial
Sequencesource/note="Description of Artificial Sequence Synthetic
oligonucleotide"modified_base(19)..(19)2'-O-methyl-modified
cmisc_feature(19)..(20)Phosphorothioate
linkagemodified_base(20)..(20)2'-O-methyl-modified a 2auugguauua
gugugugaca c 21321RNAArtificial Sequencesource/note="Description of
Artificial Sequence Synthetic oligonucleotide" 3ggccuucuuu
gaguucggug g 21423RNAArtificial Sequencesource/note="Description of
Artificial Sequence Synthetic
oligonucleotide"modified_base(21)..(21)2'-O-methyl-modified
cmodified_base(22)..(22)2'-O-methyl-modified a 4ccaccgaacu
caaagaaggc cac 23521RNAArtificial Sequencesource/note="Description
of Artificial Sequence Synthetic oligonucleotide" 5ccacaugaag
cagcacgacu u 21623RNAArtificial Sequencesource/note="Description of
Artificial Sequence Synthetic
oligonucleotide"modified_base(21)..(21)2'-O-methyl-modified
gmodified_base(22)..(22)2'-O-methyl-modified u 6aagucgugcu
gcuucaugug guc 23
* * * * *
References