U.S. patent application number 11/119059 was filed with the patent office on 2005-09-01 for methods and compositions for producing biopolymeric arrays.
Invention is credited to Schembri, Carol T..
Application Number | 20050191700 11/119059 |
Document ID | / |
Family ID | 23395020 |
Filed Date | 2005-09-01 |
United States Patent
Application |
20050191700 |
Kind Code |
A1 |
Schembri, Carol T. |
September 1, 2005 |
Methods and compositions for producing biopolymeric arrays
Abstract
Methods and compositions are provided for producing arrays of
polymeric binding agents. In the subject methods, the individual
polymers of the array are synthesized using solid phase synthesis
techniques on the surface of a substrate. A critical feature of the
invention is that one or more locations on the substrate surface
are spatially and temporally protected by a protective bubble
during the synthesis protocol, where the protective bubble may be
produced using any convenient bubble producing means. The bubble
producing means may be a component of either a substrate or a
structure separate from the substrate. Also provided are the arrays
produced by the subject methods, kits for use in practicing the
subject methods, and methods of using the arrays in analyte
detection assays, including hybridization assays, such as gene
discovery, differential gene expression and gene sequencing
assays.
Inventors: |
Schembri, Carol T.; (San
Mateo, CA) |
Correspondence
Address: |
AGILENT TECHNOLOGIES, INC.
Legal Department, DL429
Intellectual Property Administration
P. O. Box 7599
Loveland
CO
80537-0599
US
|
Family ID: |
23395020 |
Appl. No.: |
11/119059 |
Filed: |
April 28, 2005 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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11119059 |
Apr 28, 2005 |
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09997564 |
Nov 28, 2001 |
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6887715 |
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09997564 |
Nov 28, 2001 |
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09354816 |
Jul 16, 1999 |
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6346423 |
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Current U.S.
Class: |
435/6.11 ;
427/2.11; 435/91.2; 506/9 |
Current CPC
Class: |
B01J 2219/00653
20130101; B01J 2219/00531 20130101; B01J 2219/00497 20130101; Y10T
436/143333 20150115; B01J 19/0046 20130101; C07B 2200/11 20130101;
B01J 2219/00585 20130101; B01J 2219/00722 20130101; B82Y 30/00
20130101; C40B 40/00 20130101; B01J 2219/00274 20130101; B01J
2219/00533 20130101; B01J 2219/00731 20130101; B01J 2219/00596
20130101; B01J 2219/00527 20130101; B01J 2219/00659 20130101; B01J
2219/00725 20130101; B01J 2219/00536 20130101; C07H 21/00 20130101;
B01J 2219/00675 20130101 |
Class at
Publication: |
435/006 ;
435/091.2; 427/002.11 |
International
Class: |
C12Q 001/68; C12P
019/34; B05D 003/00 |
Claims
What is claimed is:
1. A method for modifying a portion of a substrate surface, said
method comprising: (a) producing a solvent layer on said substrate
surface; (b) selectively protecting at least one site on said
substrate surface with a protective bubble; and (c) contacting said
selectively protected substrate surface with a reactive agent under
conditions sufficient for said reactive agent to react with
unprotected susceptible moieties present said substrate surface;
whereby a portion of said substrate surface is modified.
2. The method according to claim 1, wherein said method comprises
reiterating steps (b) and (c) at least one additional time.
3. The method according to claim 1, wherein said method further
comprises removing unreacted reactive agent from said substrate
surface following said contact step.
4. The method according to claim 1, wherein said protective bubble
is produced by a bubble producing means.
5. The method according to claim 4, wherein said bubble producing
means is a heating means.
6. The method according to claim 4, wherein said bubble producing
means is a component of said substrate.
7. The method according to claim 4, wherein said bubble producing
means is present on a structure separate from said substrate.
8. A method for synthesizing a plurality of polymers on a substrate
surface, said method comprising: (a) producing a solvent layer on
said substrate surface, where said substrate surface has a
plurality of individually activatable resistors associated with it;
(b) performing at least two iterations of the following steps: (1)
selectively protecting at least one site on said substrate surface
with a protective bubble by selective activation of said resistors;
(2) contacting said selectively protected substrate surface with a
reactive agent under conditions sufficient for said reactive agent
to react with unprotected susceptible moieties present on said
substrate surface; and (3) removing unreacted reactive agent from
said substrate surface; whereby a plurality of polymers are
produced on said substrate surface.
9. The method according to claim 8, wherein said reactive agent is
a deblocking agent.
10. The method according to claim 8, wherein said reactive agent is
an activated monomer.
11. The method according to claim 8, wherein said polymers are
nucleic acids.
12. A method for synthesizing a plurality of polymers on a
substrate surface, said method comprising: (a) producing a solvent
layer on said substrate surface; (b) performing at least two
iterations of the following steps: (1) selectively protecting at
least one site on said substrate surface with a protective bubble,
where said protective bubble is produced by activation of a
resistor present on a structure apart from said substrate; (2)
contacting said selectively protected substrate surface with a
reactive agent under conditions sufficient for said reactive agent
to react with unprotected susceptible moieties present on said
substrate surface; and (3) removing unreacted reactive agent from
said substrate surface; whereby a plurality of polymers are
produced on said substrate surface.
13. The method according to claim 12, wherein said reactive agent
is a deblocking agent.
14. The method according to claim 12, wherein said reactive agent
is an activated monomer.
15. The method according to claim 12, wherein said polymers are
nucleic acids.
16. The method according to claim 12, wherein said polymers are
peptides.
17. A substrate produced according to the method of claim 1.
18. A polymeric array comprising: a plurality of distinct polymers
stably associated with the surface of a substrate, wherein said
substrate comprises a plurality of individually activatable
resistors associated with said surface and at least one of said
polymers is associated with at least one of said resistors.
19. The polymeric array according to claim 18, wherein said
plurality of resistors are beneath said surface of said
substrate.
20. A nucleic acid array comprising: a plurality of nucleic acid
spots stably associated with the surface of a substrate, wherein
said substrate comprises a plurality of individually activatable
resistors beneath said surface and at least one of said nucleic
acid spots is associated with at least one of said resistors.
21. A kit for producing a polymeric array, said kit comprising: a
substrate having a plurality of activatable resistors; and a
deblocking agent.
22. The kit according to claim 21, wherein said kit further
comprises a solvent.
23. The kit according to claim 21, wherein said kit further
comprises monomeric reagents.
24. A method of detecting the presence of an analyte in a sample,
said method comprising: contacting (a) a polymeric array having a
plurality of distinct polymers stably associated with the surface
of a substrate, wherein said substrate comprises a plurality of
individually activatable resistors associated with said surface,
with (b) a sample suspected of comprising said analyte under
conditions sufficient for binding of said analyte to a
complementary polymer on said array to occur; and detecting the
presence of binding complexes on the surface of the said array;
whereby the presence of said analyte in said sample is
detected.
25. The method according to claim 24, wherein said polymer is a
nucleic acid.
26. The method according to claim 25, wherein said analyte is a
nucleic acid and said binding is by hybridization.
27. The method according to claim 24, wherein said method further
comprises activating at least one of said resistors during at least
one of said contacting and detecting steps.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a divisional of U.S. patent application
Ser. No. 09/997,564, filed Nov. 28, 2001, which is a divisional of
Ser. No. 09/354,816, filed Jul. 16, 1999, now issued U.S. Pat. No.
6,346,423 from which priority is claimed under 35 U.S.C. 120. The
entireties of these applications are incorporated herein by
reference.
INTRODUCTION
[0002] 1. Technical Field
[0003] The field of this invention is polymeric arrays.
[0004] 2. Background of the Invention
[0005] "Biochips" or arrays of binding agents, such as
oligonucleotides and peptides, have become an increasingly
important tool in the biotechnology industry and related fields.
These binding agent arrays, in which a plurality of binding agents
are present on a solid support surface in the form of an array or
pattern, find use in a variety of applications, including gene
expression analysis, drug screening, nucleic acid sequencing,
mutation analysis, and the like.
[0006] Such arrays may be prepared in a number of different ways.
For example, DNA arrays may be prepared manually by spotting DNA
onto the surface of a substrate with a micro pipette. See Khrapko
et al., DNA Sequence (1991) 1:375-388. Alternatively, the dot-blot
approach, as well as the derivative slot-blot approach, may be
employed in which a vacuum manifold transfers aqueous DNA samples
from a plurality of wells to a substrate surface. In yet another
method of producing arrays of biopolymeric molecules, a pin is
dipped into a fluid sample of the biopolymeric compound and then
contacted with the substrate surface. By using a plurality or array
of pins, one can transfer a plurality of samples to the substrate
surface at the same time. Alternatively, an array of capillaries
can be used to produce biopolymeric arrays. See WO 95/35505. In
another method of producing biopolymeric arrays, arrays of
biopolymeric agents are "grown" on the surface of a substrate in
discreet regions. See e.g. U.S. Pat. No. 5,143,854 and Fodor et
al., Science (1991) 251:767-773.
[0007] Despite the variety of different methods available for the
production of biopolymeric arrays, there are disadvantages
associated with each method. For example, current methods of
growing the polymeric agents on the surface of an array, such as
the photoresist techniques described in Fodor supra, are expensive
and require the use of specialized photosensitive protecting groups
on the phosphoramidites. As such, there is continued interest in
the development of new methods for producing polymeric arrays,
particularly in the development of new methods for growing polymers
on the surface of a substrate to produce an array.
[0008] Relevant Literature
[0009] Patents and patent applications describing arrays of
biopolymeric compounds and methods for their fabrication and/or use
include: U.S. Pat. Nos. 4,877,745; 5,143,854; 5,242,974; 5,338,688;
5,384,261; 5,405,783; 5,412,087; 5,424,186; 5,429,807; 5,436,327;
5,445,934;5,449,754; 5,472,672; 5,474,796; 5,510,270; 5,527,681;
5,529,756; 5,532,128; 5,545,531; 5,552,270; 5,554,501; 5,556,752;
5,658,802; 5,561,071; 5,599,695; 5,624,711; 5,639,603; 5,658,734;
5,670,322; 5,677,195; 5,698,089; 5,700,637; 5,723,320; 5,744,305;
5,759,779; 5,763,170; 5,846,708; WO 90/10716; WO 92/10588; WO
93/17126; WO 95/11995; WO 95/35505; WO 97/10365; WO 97/27317; WO
97/46313; EP 0 373 203 B1; EP 742 287 A2; and EP 799 897 A1.
SUMMARY OF THE INVENTION
[0010] Methods and compositions for making polymeric arrays are
provided. In the subject methods, polymers are produced through the
sequential covalent addition of polymeric subunits to a growing
polymer chain on the surface of a substrate, where one or more
locations of the substrate surface are selective protected (both
spatially and temporally) by a protective bubble during the
sequential synthesis protocol. The protective bubble may be
produced on the surface in any convenient manner, including through
activation of bubble producing means, e.g. resistors, stably
associated with a surface of the substrate or part of a structure
separate from the substrate. A variety of different types of
polymeric arrays can be produced according to the subject methods,
including polypeptide and nucleic acid arrays. The subject arrays
find use in a variety of different analyte detection applications,
including hybridization assays, where specific applications include
gene discovery, differential expression and nucleic acid sequencing
assays.
Definitions
[0011] The term "nucleic acid" as used herein means a polymer
composed of nucleotides, e.g. deoxyribonucleotides or
ribonucleotides.
[0012] The terms "ribonucleic acid" and "RNA" as used herein mean a
polymer composed of ribonucleotides.
[0013] The terms "deoxyribonucleic acid" and "DNA" as used herein
mean a polymer composed of deoxyribonucleotides.
[0014] The term "oligonucleotide" as used herein denotes single
stranded nucleotide multimers of from about 10 to up to about 100
nucleotides in length.
[0015] The term "polynucleotide" as used herein refers to a single
or double stranded polymer composed of nucleotide monomers of
generally greater than 100 nucleotides in length and up to about
8,000 or more nucleotides in length.
[0016] The term "peptide" as used herein refers to any compound
produced by amide formation between a carboxyl group of one amino
acid and an amino group of another group.
[0017] The term "oligopeptide" as used herein refers to peptides
with fewer than about 10 to 20 residues, i.e. amino acid monomeric
units.
[0018] The term "polypeptide" as used herein refers to peptides
with more than 10 to 20 residues.
[0019] The term "protein" as used herein refers to polypeptides of
specific sequence of more than about 50 residues.
[0020] The term "array" as used herein means an substrate having a
plurality of binding agents stably attached to its surface, where
the binding agents may be spatially located across the surface of
the substrate in any of a number of different patterns.
[0021] The term "binding agent" means any agent that is a member of
a specific binding pair, where such agents include: peptides, e.g.
proteins or fragments thereof; nucleic acids, e.g.
oligonucleotides, polynucleotides; and the like; etc.
DESCRIPTION OF THE SPECIFIC EMBODIMENTS
[0022] Methods and compositions are provided for producing arrays
of polymeric binding agents. In the subject methods, the individual
polymers of the array are synthesized using solid phase synthesis
techniques on the surface of a substrate. A critical feature of the
invention is that one or more locations on the substrate surface
are spatially and temporally protected by a protective bubble
during the synthesis protocol, where the protective bubble may be
produced using any convenient bubble producing means. The bubble
producing means may be a component of either a substrate or a
structure separate from the substrate. Also provided are the arrays
produced by the subject methods, kits for use in practicing the
subject methods, and methods of using the arrays in analyte
detection assays, including hybridization assays, such as gene
discovery, differential gene expression and gene sequencing
assays.
[0023] Before the subject invention is described further, it is to
be understood that the invention is not limited to the particular
embodiments of the invention described below, as variations of the
particular embodiments may be made and still fall within the scope
of the appended claims. It is also to be understood that the
terminology employed is for the purpose of describing particular
embodiments, and is not intended to be limiting. Instead, the scope
of the present invention will be established by the appended
claims.
[0024] In this specification and the appended claims, the singular
forms "a," "an," and "the" include plural reference unless the
context clearly dictates otherwise. Unless defined otherwise, all
technical and scientific terms used herein have the same meaning as
commonly understood to one of ordinary skill in the art to which
this invention belongs.
[0025] The subject invention provides methods for fabricating
arrays of polymeric agents. The subject invention can be used to
fabricate a number of different types of arrays in which a
plurality of distinct polymeric binding agents are stably
associated with at least one surface of a substrate. The polymeric
binding agents may vary widely, where the only limitation is that
the polymeric binding agents are capable of being fabricated in a
step-wise fashion in which sub-units of the polymer, e.g. monomeric
units, submonomers, macromonomers (i.e. compounds of two or more,
usually no more than 10 and more usually no more than 8 monomers),
are sequentially added to each other to form a growing polymeric
chain to ultimately produce a polymeric molecule. Polymeric binding
agents of particular interest include biopolymeric molecules, such
as peptides, nucleic acids, polysaccharides and the like, where
peptides and nucleic acids are of particular interest in many
embodiments.
[0026] A critical feature of the subject methods is that protective
bubbles are positioned on the surface of the substrate both
spatially and temporally during the synthesis protocol in order to
control the nature (i.e. sequence) of the polymers that are
produced on the substrate surface. By spatially is meant that the
location of the protective bubble(s) is selected in a specific
manner, such that the protective bubble protects discrete and
defined locations on the support surface during polymer synthesis.
By temporally is meant that the duration and life of the protective
bubble is selected such that a location on the substrate surface
may be protected at one stage during synthesis and not protected at
a second stage during synthesis. By modulating the location of the
protective bubbles on the surface of the substrate during
synthesis, arrays of polymers of defined sequence and location are
produced.
[0027] The substrate surface may be protected with protective
bubbles using any convenient means. Generally, a protective bubble
producing means is employed to produce the protective bubble(s)
that selectively protect one or more locations of the substrate
surface at a given time during polymer synthesis. Although any type
of bubble producing means that is capable of being activated to
produce a bubble in a solvent layer positioned above the surface of
the substrate during polymer synthesis may be employed, the bubble
producing means is generally a heating means. In many embodiments,
the heating means is a resistor. For convenience, the subject
invention is now further described in terms of these embodiments in
which the bubble producing means is a resistor.
[0028] The protective bubble producing means employed to produce
the protective bubble(s) may incorporated into either the substrate
or a structure separate from the substrate, with the only
requirement being that the bubble producing means must be capable
of protecting the substrate surface at the desired location and
time during the synthesis process. Thus, in a first embodiment of
the invention, the bubble producing means is a component of the
substrate on which the polymers are grown, e.g. resistors are
components of the substrate, as described in greater detail below.
In a second embodiment, the bubble producing means (e.g. resistor)
is a component of a structure separate from the substrate, such as
a second plate that is brought into sufficient proximity of the
substrate surface during synthesis, as described in greater detail
below.
[0029] The substrate employed in the subject invention may be any
convenient configuration, but generally has a planar configuration.
By "planar configuration" is meant that the substrate has at least
one planar surface, which surface may have any convenient
cross-sectional shape, including circular, oval, square,
rectangular and the like. In many embodiments, the substrate has a
plate-like configuration, such as is found in a disk, rectangular
slide, square slide, and the like. In many embodiments in which the
ultimate array is to have a planar configuration, the substrate
comprises at least one planar surface that has a cross-sectional
area of at least about 4 mm.sup.3, usually at least about 16
mm.sup.2 and more usually at least about 25 mm.sup.2, where the
cross-sectional area of the planar surface may be as large as 2500
mm.sup.2 or larger, but generally does not exceed about 900
mm.sup.2 and usually does not exceed about 400 mm.sup.2. In those
embodiments where the planar surface has a square or rectangular
shape, the planar surface has a length of from about 2 to 50 mm,
usually from about 4 to 30 mm and more usually from about 5 to 20
mm, and has a width ranging from about 2 to 50 mm, usually from
about 4 to 30 mm and more usually from about 5 to 20 mm. The
substrate thickness may vary considerably, depending on the
detection protocol, i.e. whether detection is through the substrate
or just on the surface. For example, where the array is to be read
through the substrate, the thickness generally ranges from about
0.7 to 1.2 mm. Alternatively, where the array is to be surface
read, the thickness is generally dictated by the substrate
fabrication process.
[0030] In the first embodiment of the subject invention mentioned
above, the substrate employed in the subject methods is a substrate
that has a plurality of distinct, individually controllable
resistors associated with at least one of its surfaces, i.e. the
surface on which it is desired to place one or more polymeric
compounds. More particularly, the substrate in this first
embodiment is generally made up of a base material having a
plurality of resistors positioned on at least one surface thereof
and then coated with an insulating layer that is modified, as
necessary, to provide for any surface chemistry requisite for
production of the polymer molecules on the substrate surface. The
base material of the substrate is fabricated from any convenient
material or materials, where the substrate may be a pure material
or a composite structure of two or more different materials. As
indicated above, the substrate can be fabricated from any material
on which a plurality of resistors can be surface mounted. Suitable
materials therefore include silicon, fused glass, silica, and the
like. Ideally, the substrate will have a surface that provided at
most low background fluorescence.
[0031] On at least one surface of the base material, generally the
planar surface of the base material, are a plurality of
individually activatable resistors. By plurality is meant at least
2, usually at least 10 and more usually at least 100, where the
number of resistors present on the substrate surface may be as high
as 100,000 or higher, but generally does not exceed about 20,000
and usually does not exceed about 10,000.
[0032] The resistors are generally positioned on the planar surface
of the base material in the form of a pattern. Where the resistors
are positioned on the base material in the form of a pattern, the
pattern may vary as desired. As such, the pattern may be in the
form of organized rows and columns of resistors, e.g. a grid of
resistors, across the base material surface, a series of
curvilinear rows across the substrate surface, e.g. a series of
concentric circles or semi-circles of resistors, and the like.
[0033] The spacing of the resistors on the base material surface is
sufficient to provide a density of at least about 1000/cm.sup.2,
usually at least about 2000/cm.sup.2 and more usually at least
about 2500/cm.sup.2, where the density may be as great as
40,000/cm.sup.2 or greater, but generally does not exceed about
10,000/cm.sup.2 and usually does not exceed about 4,000/cm.sup.2.
In many embodiments the distance between any two given resistors on
a base material surface is at least about 50 .mu.m, usually at
least about 100 .mu.m and more usually at least about 160 .mu.m,
where the distance between any two adjacent resistors on the base
material surface may be as great as 1 mm or greater, but generally
does not exceed about 0.5 mm and usually does not exceed about 0.3
mm.
[0034] The resistors may be fabricated from any convenient material
that is capable of undergoing a sufficient rise in temperature
following application of an appropriate electrical current. As
such, any material that is capable of achieving a temperature of at
least about 50.degree. C., usually at least about 90.degree. C. and
more usually at least about 110.degree. C. upon application of an
electrical current having a magnitude of from about 1 to 100 mA,
usually from about 10 to 50 mA, may be employed. Suitable materials
from which the resistors may be fabricated include: tantalum
nitride, tantalum aluminum alloy, and the like.
[0035] Each of the resistors is individually activatable. By
individually activatable is meant that the temperature of each
resistor may be raised or lowered separately from any other
resistor present on the substrate. As such, means for providing the
requisite electrical current to each resistor are present on the
base material surface, where such means may be any current
communication means, such as stripes of a conducting material, etc.
The means for applying electrical current to each resistor further
includes a means for controlling which resistors are activated and
which are not, i.e. a switching means for directing electrical
current to the appropriate resistors associated with the substrate
surface. A variety of suitable means as described above are known
in the integrated circuit art and may be employed.
[0036] Positioned over the surface of the resistors on the base
material is an insulating material, i.e. an insulator layer. The
insulator material may be any convenient, non-conductive material
or a composite of two or more inert materials, where suitable inert
materials include silicon dioxide, silicon nitride, silicon carbide
and the like, with silicon dioxide being preferred, with the only
proviso being that the surface of the insulator layer must be
susceptible to modification such that attachment of polymers to the
surface can be achieved during polymer synthesis. The thickness of
the insulator layer is typically at least about 0.1 and more
usually at least about 0.2 .mu.m, where the insulator layer may
have a thickness as great as 2.0 .mu.m or greater, but will
generally not exceed about 1.5 .mu.m and usually will not exceed
about 1.0 .mu.m. As such, the plurality of the resistors is
associated with the substrate surface, and more specifically is
beneath the substrate surface, i.e. underneath the insulating layer
of the substrate.
[0037] The surface of the insulator layer is generally modified to
provide for surface groups that allow for covalent attachment of
the polymeric subunits onto the insulator layer during fabrication
of the arrays. Surface reactive groups that may be introduced onto
the surface of the insulating layer include: amino, e.g. primary
amino; hydroxyl; thiol; sulfonic acid; phosphorous and phosphoric
acid, particularly in the form of acid halides; especially chloride
and bromide; and the like. The reactive groups may introduced onto
the surface of the substrate using any convenient protocol, such as
the protocols described in U.S. patent application Ser. No.
09/145,015 filed Sep. 1, 1998, the disclosure of which is herein
incorporated by reference.
[0038] The above substrates may be fabricated using any convenient
protocol, where standard IC fabrication and surface chemistry
modification protocols are generally employed. A representative
protocol is as follows is provided in the experimental section
infra.
[0039] In the second embodiment, the substrate is not limited as in
the first embodiment, in that the substrate employed in the second
embodiment does not include a plurality of resistors. Instead, the
bubble producing means, e.g. resistors, are present on a structure
separate from the substrate, as summarized above. As such, the
substrate may be any convenient substrate that finds use in
biopolymeric arrays. In general, the substrate is rigid substrate
in this second embodiment. By rigid is meant that the support is
solid and does not readily bend, i.e. the support is not flexible.
As such, rigid substrates are sufficient to provide physical
support and structure to the nucleic acid spots present thereon.
Furthermore, when the rigid supports of the subject invention are
bent, they are prone to breakage. The substrates may be fabricated
from a variety of materials. In certain embodiments, e.g. where one
is interested in the production of nucleic acid arrays for use in
research and related applications, the materials from which the
substrate may be fabricated should ideally exhibit a low level of
non-specific binding during hybridization events. In many
situations, it will also be preferable to employ a material that is
transparent to visible and/or UV light. For rigid substrates,
specific materials of interest include: silicon; glass; plastics,
e.g. polytetrafluoroethylene, polypropylene, polystyrene,
polycarbonate, and blends thereof, and the like; metals, e.g. gold,
platinum, and the like; etc. The surface may be modified with one
or more different layers of compounds that serve to modify the
properties of the surface in a desirable manner. Such modification
layers, when present, will generally range in thickness from a
monomolecular thickness to about 1 mm, usually from a monomolecular
thickness to about 0.1 mm and more usually from a monomolecular
thickness to about 0.001 mm. Modification layers of interest
include: inorganic and organic layers such as metals, metal oxides,
conformal silica or glass coatings, polymers, small organic
molecules and the like. Polymeric layers of interest include layers
of: peptides, proteins, polynucleic acids or mimetics thereof, e.g.
peptide nucleic acids and the like; polysaccharides, phospholipids,
polyurethanes, polyesters, polycarbonates, polyureas, polyamides,
polyethyleneamines, polyarylene sulfides, polysiloxanes,
polyimides, polyacetates, and the like, where the polymers may be
hetero- or homopolymeric, and may or may not have separate
functional moieties attached thereto, e.g. conjugated. The
particular surface chemistry will be dictated, as in the first
embodiment, by the specific process to be used in polymer
synthesis, as described in greater detail infra.
[0040] Turning now to the subject methods for producing arrays, the
first step of the subject methods is to produce a solvent layer on
at least one surface of the array, i.e. the surface on which the
polymers are to be synthesized. The solvent layer may be produced
on the surface of the substrate by any convenient protocol, such as
by immersing the substrate in a container of the solvent, flooding
the surface of the array with the solvent and the like. As such,
the thickness of the solvent layer may vary widely, as long as it
is sufficiently thick to provide for a suitable environment for the
polymeric production chemistry to occur on the substrate surface
coated with the solvent layer. In other words, the solvent layer
must be of sufficient thickness to provide a suitable fluid
environment for the polymeric synthesis chemical reactions to
occur. Where the surface of the substrate is flooded with the
solvent layer, the thickness of the solvent layer is generally at
least about 100 .mu.m, usually at least about 1 mm thick, where the
thickness may be as great as 3 mm or greater, but generally does
not exceed about 2.5 mm and usually does not exceed about 2 mm.
[0041] The solvent of the solvent layer is generally selected based
on the particular chemistry to be performed in production of the
polymeric binding agents. As such, depending on the particular
chemical reactions to be performed during the synthesis of the
polymers on the substrate surface, the solvent layer may be aqueous
or non-aqueous. For example, the solvent layer may be aqueous in
those situations where the solid phase polymeric synthesis
protocols do not require anhydrous conditions. Aqueous solvents of
interest include pure water, a water in combination with a
co-solvent, e.g. an organic co-solvent, and the like. Where
anhydrous conditions are required, e.g. in nucleic acid synthesis,
non-aqueous solvents are employed. Non-aqueous solvents of interest
include organic solvents, such as tetrahydrofuran, acetonitrile,
dichloromethane, and the like, where acetonitrile is preferred in
many embodiments, e.g. in the production of nucleic acid
arrays.
[0042] Following production of the solvent layer on the substrate
surface, the substrate surface is selectively protected. By
"selectively protected" is meant that a portion of, but not all of,
the potential reactive sites on the substrate surface (i.e. the
sites containing covalently bound susceptible reactive moieties)
are protected from reaction. As such, following selective
protection of the substrate surface, only a portion of the
potential susceptible reactive groups present on the substrate
surface are actually available for reaction with a corresponding
reactive group, i.e. a group that reacts with the surface bound
susceptible moiety.
[0043] The substrate surface is selectively protected with one or
more protective bubbles positioned on the surface at sites where
prevention of reaction between surface bound susceptible groups and
reactive agents in the solvent layer is desired. The protective gas
bubbles are produced at a desired site(s) on the substrate surface
to achieve selective protection of the substrate surface in any
convenient manner.
[0044] In the first embodiment of the subject invention (i.e. where
the substrate comprises a plurality of individually activatable
resistors), selective protection of one or more sites is achieved
by activating the resistor associated with the substrate surface at
each site where protection is desired, i.e. by selectively
activating the resistors associated with the substrate surface. In
selectively activating the resistors associated with the substrate
surface, only a portion of the total number of resistors is
activated, where the portion that are activated are those that
underlie the surface at the site at which protection is
desired.
[0045] In the second embodiment of the subject invention, as
summarized above the resistors (or other bubble producing means)
are present on a structure that is separate from the substrate.
Typically, though not necessarily, the resistors are present on a
plate like structure of analogous proportions and composition to
the substrate of the first embodiment (with the exception that the
surface need not be modified to provide for functional groups
employed in the polymer synthesis protocol), such that the
resistors can be lined up with discrete and known locations of the
substrate to protect these locations at various stages during the
synthesis. In these embodiments, the structure comprising the
resistors is brought within sufficiently close proximity to the
substrate surface such that the bubble which nucleates on the
separate structure is capable of touching and covering a reactive
site on the substrate.
[0046] The resistors (present on either the substrate or the
separate structure, as described above) are selectively activated
by applying an electrical current to those resistors located at the
site of either the substrate surface to be protected or on the
separate structure immediately opposite the substrate surface
location to be protected. The surface area of the substrate covered
by each bubble, i.e. the surface area of the substrate at which
solvent is prevented from having contact with the susceptible
moieties stably attached thereto, generally ranges from about 100
to 62,500 .mu.m.sup.2, usually from about 625 to 22500 .mu.m.sup.2,
and more usually from about 2500 to 10,000 .mu.m.sup.2. The
electrical current applied to the resistor in the production of the
protective bubble is sufficient to raise the temperature of
resistor such that a protective bubble of desired volume is
produced, where the temperature of the resistor varies depending on
the nature of the solvent layer.
[0047] Following selective protection of the substrate surface, the
selectively protected surface is contacted with a reactive agent
that is capable of reacting with unprotected susceptible groups on
the substrate surface. Contact may be achieved by any convenient
means. Typically, the reactive agent is introduced into the solvent
layer on the surface of the substrate in a manner that does not
disrupt the protective bubble(s). Contact is maintained for a
sufficient period of time and under sufficient conditions for the
reactive agent to react with substantially all of the unprotected
susceptible moieties present on the substrate surface. This
incubation period varies depending on the nature of the reaction
being performed, but generally lasts for a period of time ranging
from about 5 sec to 10 min, usually from about 10 sec to 5 min and
more usually from about 10 sec to 1 min. Contact of the selectively
protected substrate surface with the reactive agent results in the
surface modification of a portion of, but not all of, the substrate
surface. In other words, the portion of the substrate surface not
selectively protected by the protective bubble(s) is chemically
modified, e.g. by the addition of a monomeric residue or by the
removal of a protective group depending on whether the reactive
agent is an activated monomer or a deblocking agent, following
contact with the reactive agent.
[0048] Following contact of the substrate layer with the reactive
agent and the passage of a sufficient period of time for all
potential reactions between the reactive agent and unprotected
susceptible moieties present on the substrate surface to occur, any
remaining reactive agent (i.e. un-reactive reactive agent) is
removed from the substrate surface. Removal of the un-reacted agent
from substrate surface may be accomplished using any convenient
methodology. Thus, one may use washing protocols to remove the
un-reacted reactive agent. Washing protocols may involve replacing
the solvent layer present on the substrate surface with a fresh
solvent layer, flooding the substrate surface with fresh solvent so
to displace essentially all of the prior solvent, and the like.
During or after the washing procedure, depending on the particular
protocol employed, the selective activated resistors are
deactivated. As such, following the washing procedure, one obtains
a substrate surface that has been selectively modified, e.g.
protective groups removed or polymeric subunit covalently attached,
in those areas that were not protected by the protective
bubbles.
[0049] Following washing, the entire substrate surface is contacted
with the next reactive agent in the polymeric synthesis protocol,
e.g. an activated monomer such as a nucleotide where the initial
reactive agent contacted with the selectively protected substrate
surface is a deblocking agent; or a deblocking agent such as
dichloroacetic acid or trichloroacetic acid where the initial
reactive agent is an activated nucleotide. Contact between this
second reactive agent and the substrate surface is maintained for a
period of time sufficient for any potential reactions to occur
between this second reactive agent and susceptible moieties on the
substrate surface. As in the first step, un-reacted reactive agent
is then removed from the substrate surface following this
incubation step, e.g. by washing.
[0050] By reiterating or repeating the above synthesis steps of
selective protection, reagent contact with the selectively
protected surface, washing, and reagent contact with entire surface
(which is not selectively protected), polymeric compounds are grown
at various positions on the surface of the substrate. By
controlling the nature of the reactive agents and the selective
protection of the surface, an array of diverse polymeric compounds
may be synthesized on the substrate surface.
[0051] As mentioned above, the subject invention can be used to
produce a number of different types of arrays, including nucleic
acid and peptide arrays. A preferred embodiment of the subject
invention is the use of the subject methods to produce nucleic acid
arrays. Nucleic acid arrays are produced according to the subject
invention by synthesizing nucleic acid polymers using conventional
phosphoramidite solid phase nucleic acid synthesis chemistry where
the solid support is a substrate as described above and protective
bubbles are employed at various stages of the step-wise synthesis
procedure to selectively protect certain sites on the substrate
surface from reaction during the synthesis protocol.
Phosphoramidite based chemical synthesis of nucleic acids is well
known to those of skill in the art, being reviewed in Streyer,
Biochemistry (1988) pp 123-124 and U.S. Pat. No. 4,415,732, the
disclosure of the latter being herein incorporated by
reference.
[0052] To produce nucleic acid arrays according to the subject
methods, a substrate surface as described above having the
appropriate surface groups, e.g. --OH groups, present on its
surface, is obtained. See the Experimental Section infra for a
representative protocol for preparing such a substrate. Since the
synthesis protocol must be carried out under anhydrous conditions,
all reactions are carried out in a non-aqueous, typically organic
solvent layer on the substrate surface, where the solvent layer is
acetonitrile in many embodiments.
[0053] Next, the first residues of each nucleic acid to be
synthesized on the array are covalently attached to the substrate
surface via the surface bound --OH groups. Depending on whether the
first nucleotide residue of each nucleic acid to be synthesized on
the array is the same or different, different protocols for this
step may be followed. Where each of the nucleic acids to be
synthesized on the substrate surface have the same initial
nucleotide at the 3' end, the entire surface of the substrate is
contacted with the appropriate activated nucleoside under
conditions sufficient for coupling of the activated nucleoside to
the reactive groups, e.g. --OH groups, present on the substrate
surface to occur. Alternatively, where the initial residue of the
various nucleic acids differs among the nucleic acids, one or more
sites on the substrate surface are initially selectively protected
with protective bubbles, as described supra, by activating the
appropriate resistors (either in the substrate or the structure
separate from the substrate, as described above). Following
selective protection of the surface, the appropriate activated
nucleotide, e.g. A, is then contacted with the substrate surface.
Next, different sites on the substrate surface are selectively
protected, followed by contact with a different activated
nucleotide, e.g. C. This process is then repeated with additional
different activated nucleotides, e.g. T & G, until all of the
initial nucleotides of each to be synthesized nucleic acids are
deposited on the substrate surface. At some point during this
initial deposition, usually following deposition of all of the
initial nucleotides, phosphite triesters present on the substrate
surface following coupling are converted to phosphotriesters, e.g.
by oxidation with a suitable oxidating agent, such as
I.sub.2/H.sub.2O. In addition, unreacted hydroxyl groups are
usually (though not necessarily) capped, e.g. using any convenient
capping agent, as is known in the art.
[0054] Following covalent attachment of the initial nucleotides of
each nucleic acid, the following two steps are performed: (1)
selectively protecting one or more positions on the substrate
surface with protective bubbles; and (2) contacting the selectively
protected surface with a reactive agent, where the reactive agent
may be a deblocking agent or an activated nucleotide. Since the
protocols vary depending on whether the reactive agent contacted
with the selectively protected surface is a deblocking agent or an
activated nucleoside phosphoramidite, each of these situations is
described separately below.
[0055] Where the reactive agent contacted with the selectively
protected substrate surface is a deblocking agent, the first step
following production of the substrate having the first monomeric
residue of each nucleic acid on its surface is to selectively
protect one or more positions on the substrate surface with
protective bubble(s). Selective protection results in a portion of
the sites on the substrate surface being exposed to the solvent
layer and a portion of the sites on the substrate surface being
"hidden" from the solvent layer. The selectively protected
substrate surface is then contacted with a deblocking or
deprotecting agent, e.g. by introducing a deblocking agent into the
solvent layer. Following introduction of the deblocking agent, the
substrate surface is incubated for a sufficient period of time
under appropriate conditions for all available protecting groups,
e.g. all protecting groups not protected, i.e. underneath, a
protective bubble, to be cleaved from the nucleotides that they are
protecting.
[0056] Contact of the selectively protected substrate surface with
a deblocking agent results in removal of the protecting groups from
those substrate bound residues not underneath a protective bubble.
As such, this step results in the deprotection of a portion of the
nucleotide residues on the substrate surface. Following
deprotection, the deblocking agent is removed from the solvent
layer on the surface of the substrate, where removal of the
deblocking agent can be accomplished using any convenient protocol.
Thus, the solvent layer may be completely removed from the
substrate surface, and then replaced with fresh solvent layer,
following one or more washing steps. Alternatively, a sufficient
amount of the solvent layer may be replaced with new solvent in a
flow through protocol in a manner sufficient to reduce the
concentration of deblocking agent present above the substrate
surface to essentially zero, e.g. by flushing the substrate surface
with fresh solvent. Either during or after this washing step, the
protective bubbles are removed, e.g. by deactivating the
selectively activated resistors on either the substrate or the
structure separate from the substrate, depending on which
embodiment of the invention is being employed.
[0057] Removal of the deblocking agent and protective bubbles
results in a substrate surface in which a portion of the bound
nucleotide residues are deprotected and a portion of the bound
nucleotide residues are protected. In others words, removal of the
protective bubbles and deblocking agent results in the production
of an array of nucleotide residues stably associated with the
substrate surface, where a portion of the nucleotide residues on
the array surface have --OH groups available for reaction with an
activated nucleotide.
[0058] The next step in the subject methods is to contact this
selectively deprotected array of surface bound nucleotides with an
activated nucleotide under conditions sufficient for coupling
between the activated nucleotide and the deprotected surface bound
nucleotide to occur. Contact of the selectively protected surface
with the activated nucleotide may be accomplished using any
convenient protocol, e.g. by contacting the surface with a solution
of the activated monomer; introducing the activated monomer into a
solvent layer already present on the substrate surface; and the
like. Contact of the selectively protected surface with the
activated nucleotide is maintained for a sufficient period of time
for coupling to occur. Coupling results in the production of a
substrate having a surface in which a portion of the surface bound
nulceic acids have been elongated by one nucleotide residue, while
the remainder have not. Next, unbound activated nucleotide is
removed from the surface, e.g. by washing. As is known in the art,
at some convenient point during the above steps, e.g. after each
coupling or after all of the couplings of a given layer, the
phosphite triesters that result from coupling are oxidized to
phosphotriesters. The only limitation on this oxidization step is
that it generally occurs prior to the addition of the next
nucleotide residue on a growing chain.
[0059] The above steps of: (a) selective protection; (b) contact of
the selectively protected surface with a deblocking agent; and (c)
contact of the entire surface with an activated nucleotide are
repeated with additional nucleotides until each of the desired
nucleic acids on the substrate surface are produced. By choosing
which sites are protected at each selective protection step as well
as which activated nucleotides, e.g. A, G, C & T, are contacted
with the entire substrate surface, an array having polymers of
desire sequence and spatial location is readily achieved.
[0060] The above protocol varies somewhat where the reactive agent
that is contacted with the selectively protected surface is the
activated nucleotide. In this embodiment, the first step in the
synthesis of the nucleic acids, following stable attachment of the
terminal nucleotides to the substrate surface, is to deblock all of
the nucleotides on the substrate surface, e.g. to contact the
entire surface with a deblocking agent. Following contact of the
entire surface with a deblocking agent, the surface is selectively
protected as described above, which results in a portion of the
deblocked substrate bound nucleotides being "hidden" underneath
protective bubbles. The selectively protected substrate surface is
then contacted with an activated nucleotide under coupling
conditions, whereby elongation occurs at those sites on the
substrate surface not under a protective bubble. Following
elongation, remaining activated nucleotide is removed e.g. by
washing. The surface is then selectively protected at different
locations, where at least a portion of the sites initially
protected remain unprotected by a protective bubble, and all of the
unprotected sites in the first activated nucleotide contact step
are generally (though not necessarily) protected (reaction should
not occur at these sites since they are occupied by the first
activated monomer which is protected). This second selectively
protected substrate surface is contacted with a second activated
monomer to elongate the nucleic acid present at the unprotected
sites. By reiterating these steps with the remaining activated
monomers, each of the nucleic acids on the array is elongated by
one residue. Thus, this protocol is analogous to the first
protocol, with the only difference being that the activated monomer
is contacted with the selectively protected surface and the
deblocking agent is contacted with the entire surface. As with the
first protocol, by tailoring the selective protection and the
sequence of activated nucleotide contact, one can obtain a nucleic
acid array of any desired sequence and spatial characteristics.
[0061] As mentioned above, the subject methods (particularly of the
second embodiment) are also amenable to the production of peptide
arrays, i.e. arrays of polymeric agents which are characterized by
the presence of peptide bonds. Any convenient solid phase peptide
synthesis protocol may adapted to practice the subject methods,
where the resistor comprising substrates of the subject methods are
employed as the solid phase. Jones, The Chemical Synthesis of
Peptides (Oxford University Press)(1993) provides a review of solid
phase peptide synthesis. The preparation of peptides according to
the subject methods is analogous to the preparation of nucleic
acids described above. Thus, the reactive agent contacted with the
selectively protected surface may be a deprotecting agent or an
.alpha.-amino protected amino acid. Where the reactive agent
contacted with the selectively protected surface is a deblocking or
deprotecting agent, the method further includes contacting the
entire surface of the substrate with an .alpha.-amino protected
amino acid. Conversely, where the reactive agent that is contacted
with the selectively protected surface is an .alpha.-amino
protected amino acid, the deblocking agent is contacted with the
entire surface. As with the nucleic acid synthesis, by appropriate
selection of which sites to selectively protect at a give time and
the order of contact of the .alpha.-amino protected amino acids
with the substrate surface, a peptide array of any desired spatial
and sequence characteristics may be obtained.
[0062] The subject methods result in the production of arrays of
polymeric binding agents, e.g. nucleic acid arrays, peptide arrays,
etc. The density and overall number of the polymeric binding agents
on the substrate surface may vary greatly. Because of the methods
by which the subject arrays are produced, the length of each
polymer on the substrate surface of the arrays generally does not
exceed about 50 monomeric units, usually does not exceed about 35
monomeric units and more usually does not exceed about 25 monomeric
units. In those arrays produced according to the first embodiment
of the subject invention, described above, a plurality of resistors
are associated with the surface of the substrate to which the
polymeric binding agents are stably attached.
[0063] The subject arrays find use in a variety applications, where
such applications are generally analyte detection applications in
which the presence of a particular in a given sample is detected at
least qualitatively, if not quantitatively. Protocols for carrying
out such assays are well known to those of skill in the art and
need not be described in great detail here. Generally, the sample
suspected of comprising the analyte of interest is contacted with
an array produced according to the subject methods under conditions
sufficient for the analyte to bind to its respective binding pair
member that is present on the array. Thus, if the analyte of
interest is present in the sample, it binds to the array at the
site of its complementary binding member and a complex is formed on
the array surface. The presence of this binding complex on the
array surface is then detected, e.g. through use of a signal
production system, e.g. an isotopic or fluorescent label present on
the analyte, etc. The presence of the analyte in the sample is then
deduced from the detection of binding complexes on the substrate
surface.
[0064] Specific analyte detection applications of interest include
hybridization assays in which the nucleic acid arrays of the
subject invention are employed. In these assays, a sample of target
nucleic acids is first prepared, where preparation may include
labeling of the target nucleic acids with a label, e.g. a member of
signal producing system. Following sample preparation, the sample
is contacted with the array under hybridization conditions, whereby
complexes are formed between target nucleic acids that are
complementary to probe sequences attached to the array surface. The
presence of hybridized complexes is then detected. Specific
hybridization assays of interest which may be practiced using the
subject arrays include: gene discovery assays, differential gene
expression analysis assays; nucleic acid sequencing assays, and the
like.
[0065] Where the subject arrays are arrays having a plurality of
resistors incorporated into the substrate, e.g. such as those
produced according to the first embodiment of the subject
invention, assays can be performed in which one or more of the
resistors is selectively activated to modulate the temperature of
the reaction solution above the substrate surface, e.g. during
hybridization or detection. For example, the resistors could be
heated to different temperatures to get the desired stringency for
each probe type during a nucleic acid hybridization reaction.
Alternatively, for polymorphism analysis, melt-off experiments may
be performed. In such experiments, the hybridization is allowed to
proceed and then the array is scanned wet. Then each resistor is
slowly heated while the array is rescanned. As the probe/target
pairs are heated, they will separate and the signal at each feature
will drop. The signal is plotted relative to temperature (or
voltage applied to the resistor). The point of inflection on the
curve is called T.sub.m or the melting point of the probe/target
hybridization. At this point, half of the probe/target pairs have
separated. T.sub.m gives a measure of the binding strength of the
hybridization. Exact compliments have higher T.sub.m's than pairs
with mismatches such as single base changes, additions or
deletions.
[0066] Also provided by the subject invention are kits for use in
producing the subject arrays. Kits for producing the subject arrays
generally include at least a substrate having a plurality of
individually activatable resistors associated with a surface
thereof. The kits may further include various reagents that are
employed in the polymeric synthesis protocol, e.g. deblocking
agent, monomers, e.g. DMT protected nucleotide phosphoramidites,
activating agents, solvents, oxidizing agents, and the like. In
addition, the kits typically further include instructions for how
to synthesize a polymeric array according to the subject methods,
where these instructions are generally present on at least one of a
package insert and the package of the kit.
[0067] Finally, kits for use in analyte detection assays are
provided. The subject kits at least include the arrays of the
subject invention. The kits may further include one or more
additional components necessary for carrying out the analyte
detection assay, such as sample preparation reagents, buffers,
labels, and the like. In addition, the kits typically further
include instructions for how practice the subject analyte detection
methods according to the subject invention, where these
instructions are generally present on at least one of a package
insert and the package of the kit.
[0068] The following examples are offered by way of illustration
and not by way of limitation.
EXPERIMENTAL
[0069] I. Preparation of a Resistor Substrate for Use in the
Synthesis of Nucleic Acid Arrays
[0070] A resistor substrate is prepared according to the method
described in U.S. Pat. No. 4,809,428, the disclosure of which is
herein incorporated by reference, with the only difference being
that the barrier layer is not applied. Instead another coating of
SiO.sub.2 is applied in thickness ranging from about 0.25-1 micron.
The surface of then functionalized according to the process
disclosed in U.S. patent application Ser. No. 09/145,015, filed
Sep. 1, 1998, the disclosure of which is herein incorporated by
reference, to provide for surface --OH groups.
[0071] II. Production of Nucleic Acid Arrays.
[0072] Nucleic acid arrays are synthesized on the functionalized
surface of resistor substrates, as described above, according to
the following methods.
[0073] A. Protecting at the Phosphoramidite Addition Step.
[0074] The substrate is built as described in Section I above
through the addition of the two passivation layers, where the
SiO.sub.2 layer is added only in the region of the resistors. As
such, the addition of the linker chemistry only occurs on the
SiO.sub.2 layer. The linker chemistry does not have any protecting
group and ends in a hydroxyl, thereby providing the requisite
surface --OH moieties required for synthesis of the nucleic
acids.
[0075] The surface is flooded in acetonitrile. Bubbles are formed
over the features that will not couple the first phosphoramidite.
The acetonitrile is exchanged with acetonitrile that contains the
first phosphoramidite. The coupling reaction occurs. The
phosphoramidite solution is removed by exchange with neat
acetonitrile. The resistors are turned off. Any remaining bubbles
are washed off by the capping solutions that flood the surface. The
process is repeated for the three remaining phosphoramidites such
that all of the sites have a first base coupled. After the last
coupling, the surface is flooded with the oxidizing reagents
(capping if employed) and then the deblocking reagents. The process
is repeated for the second round of base additions.
[0076] B. Protecting at the Deblock Step.
[0077] In this embodiment, the surface of the resistor substrate as
describe in Section I above is modified such that the surface
linker includes a protecting group, such as dimethyloxytrityl. It
is assumed that the active surface covers the entire surface, the
area over the resistors and the area between the resistors. The
first step is to inactivate the area between the resistors. The
surface is flooded with dichloromethane. Bubbles are formed at all
of the resistor locations. The solvent is exchanged with 3%
dichloroacetic acid or trichloroacetic acid in dichloromethane to
deblock the non-resistor surfaces. The solvent is exchanged with
dichloromethane and the resistors are turned off. The surface is
flooded with the capping reagents to cap all the hydroxyls between
the features. The synthesis process can now start. The surface is
again flooded with dichloromethane. Bubbles are formed at those
resistor locations that will not be receiving the first
phosphoramidite. The solvent is exchanged with 3% trichloroacetic
acid in dichloromethane to deblock those sites that will receive
the first phosphoramidite. Again the solvent is exchanged with
dichloromethane and the resistors are turned off. The
dichloromethane is removed and the surface is flooded with the
first phosphoramidite. It can couple only at the sites that were
deprotected. The phosphoramidite is removed and the surface is
flooded with the capping solutions. These solutions are removed and
the surface is flooded with the oxidation reagents. These reagents
are removed and the process is started again. The next set of
features is deprotected and the second phosphoramidite is added.
Normally, the process must be repeated four times to get a single
base addition at each location. The process is repeated until
oligos of the desired length are built at each feature.
[0078] The resultant nucleic acid arrays find use in variety of
hybridization applications, as describe supra.
[0079] It is evident from the above results and discussion that a
simple and efficient way to prepare polymeric arrays is provided.
Because the substrate is selectively protected by protective
bubbles at appropriate stages during the polymeric synthesis
process, all of the steps in the synthesis process are alignment
independent, which is a distinct advantage over prior art methods,
particularly those in which large numbers of distinct polymers are
to be positioned on the substrate surface. Furthermore, the subject
methods are readily adaptable to automated systems. As such, the
subject invention is a significant contribution to the art.
[0080] All publications and patent applications cited in this
specification are herein incorporated by reference as if each
individual publication or patent application were specifically and
individually indicated to be incorporated by reference. The
citation of any publication is for its disclosure prior to the
filing date and should not be construed as an admission that the
present invention is not entitled to antedate such publication by
virtue of prior invention.
[0081] Although the foregoing invention has been described in some
detail by way of illustration and example for purposes of clarity
of understanding, it is readily apparent to those of ordinary skill
in the art in light of the teachings of this invention that certain
changes and modifications may be made thereto without departing
from the spirit or scope of the appended claims.
* * * * *