Systems tools and methods of assaying biological materials using spatially-addressable arrays
First Claim
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1. An assay system for multiplexing together on a single array a plurality of different biological samples having one biological target per sample or a plurality of different biological targets per sample, comprising:
- an array apparatus that comprises a plurality of first biological probes on a substrate in an array pattern of features, wherein each first probe is different from others in the plurality of first probes, each different first probe is located at a different feature location of the array and is a different address on the array; and
a plurality of second biological probes, each second probe comprising a first region and a second region, each second probe being different from others in the plurality of second probes by comprising a different first region, wherein the first region of each second probe is complementary to a different first probe, and the second region of each second probe is complementary to a specific target, such that each second probe addresses a complementary specific target from a different sample of the plurality of different samples being assayed to one of the different addresses on the array corresponding to a respective complementary different first probe.
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Abstract
Systems, tools and methods of assaying biological material are used to perform complex sandwich hybridization assays. The tools used comprise biological solution probes that are customized for each assay. The solution probe comprises a first region for hybridizing to a probe, in a generic set of capture probes on a universal assay apparatus, and a second region for hybridizing to a target in a sample. The solution probe assembles the target to the assay apparatus by hybridizing the second region to the target and the first region to the capture probe. In array assays, one or more biological samples, having one or more targets per sample, can be multiplexed on the same universal array comprising the generic set of capture probes in an array pattern of features on the substrate. The customized solution probe addresses and assembles a predetermined target-sample combination onto the array at a corresponding capture probe address location. The systems, tools and methods have specificity and sensitivity by systematically providing a reduced likelihood of cross-hybridizations and intramolecular structures in the probes. Specificity and sensitivity of the assay are provided by the incorporation of a chemically modified monomer in the capture probe and a similarly modified monomer complement in the first region of the solution probe. The modified monomers preferentially hybridize with each other. When the probe and respective probe region are oligonucleotides, the complementary modified nucleotides have a reversed polarity relative to the polarity of the respective probe and probe region. The complementary reversed polarity nucleotides form a thermodynamically more stable hybridization to each other than a hybridization between the reversed polarity nucleotide and a complementary nucleotide whose polarity is not similarly reversed.
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Citations
28 Claims
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1. An assay system for multiplexing together on a single array a plurality of different biological samples having one biological target per sample or a plurality of different biological targets per sample, comprising:
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an array apparatus that comprises a plurality of first biological probes on a substrate in an array pattern of features, wherein each first probe is different from others in the plurality of first probes, each different first probe is located at a different feature location of the array and is a different address on the array; and
a plurality of second biological probes, each second probe comprising a first region and a second region, each second probe being different from others in the plurality of second probes by comprising a different first region, wherein the first region of each second probe is complementary to a different first probe, and the second region of each second probe is complementary to a specific target, such that each second probe addresses a complementary specific target from a different sample of the plurality of different samples being assayed to one of the different addresses on the array corresponding to a respective complementary different first probe. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 11, 24, 25, 26)
wherein the oligonucleotide first probes comprise a plurality of first nucleotides having either a (3′ - →
5′
) or (5′
→
3′
) polarity, and a first modified nucleotide that has a reversed polarity with respect to the polarity of the plurality of first nucleotides, and
wherein the oligonucleotide regions of the second probes comprise a plurality of second nucleotides having the same polarity as the polarity of the plurality of first nucleotides, the plurality of second nucleotides being complementary to the plurality of first nucleotides, and the second modified monomer comprises a second nucleotide that has a reversed polarity with respect to the polarity of the plurality of second nucleotides, the second reversed polarity nucleotide being complementary to the first reversed polarity nucleotide in the first probe, and wherein the complementary first reversed polarity nucleotide and the second reversed polarity nucleotide preferentially hybridize with each other instead of with a complementary nucleotide whose polarity is not similarly reversed, such that specificity and sensitivity is provided to the assay.
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9. An assay system for multiplexing on a single array one or more biological samples having one or more biological targets per sample, comprising:
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an array apparatus that comprises a plurality of first biological probes on a substrate in an array pattern of features, wherein each first probe is different from others in the plurality of first probes, each different first probe is located at a different feature location of the array and is a different address on the array; and
a plurality of second biological probes, each second probe comprising a first region and a second region, each second probe being different from others in the plurality of second probes by comprising a different first region, wherein the first region of each second probe is complementary to a different first probe, and the second region of each second probe is complementary to a target in the one or more samples, such that each second probe addresses a target from a sample being assayed to one of the different addresses on the array corresponding to a respective complementary different first probe, wherein each first probe comprises a first sequence of monomers, and wherein the first region of each second probe comprises a second sequence of monomers, and wherein the first sequence of monomers comprises a first modified monomer and the second sequence of monomers comprises a second similarly modified monomer that is complementary to the first modified monomer, wherein the modification causes the complementary first modified monomer and second modified monomer to preferentially hybridize or bind with each other instead of with a complementary monomer that is not similarly modified.
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10. An assay system for multiplexing on a single array one or more biological samples having one or more biological targets per sample, comprising:
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an array apparatus that comprises a plurality of first biological probes on a substrate in an array pattern of features, wherein each first probe is different from others in the plurality of first probes, each different first probe is located at a different feature location of the array and is a different address on the array; and
a plurality of second biological probes, each second probe comprising a first region and a second region, each second probe being different from others in the plurality of second probes by comprising a different first region, wherein the first region of each second probe is complementary to a different first probe, and the second region of each second probe is complementary to a target in the one or more samples, such that each second probe addresses a target from a sample being assayed to one of the different addresses on the array corresponding to a respective complementary different first probe, wherein the plurality of first probes comprises oligonucleotide first probes and the first regions of the plurality of second probes comprises oligonucleotide regions, and wherein the oligonucleotide first probes comprise a plurality of first nucleotides having either a (3′
→
5′
) or (5′
→
3′
) polarity, and a first modified nucleotide that has a reversed polarity with respect to the polarity of the plurality of first nucleotides, andwherein the oligonucleotide regions of the second probes comprise a plurality of second nucleotides having the same polarity as the polarity of the plurality of first nucleotides, the plurality of second nucleotides being complementary to the plurality of first nucleotides, and a second modified nucleotide that has a reversed polarity with respect to the polarity of the plurality of second nucleotides, the second reversed polarity nucleotide being complementary to the first reversed polarity nucleotide in the first probe, and wherein the complementary first reversed polarity nucleotide and the second reversed polarity nucleotide preferentially hybridize with each other instead of with a complementary nucleotide whose polarity is not similarly reversed, such that specificity and sensitivity is provided to the assay.
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12. An assay method of multiplexing together on a single array a plurality of different biological samples having one biological target per sample or a plurality of different biological targets per sample, comprising the steps of:
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providing an array apparatus having a plurality of first biological probes on a substrate in an array pattern of features, each first probe being different, each different first probe being located on a different feature location of the array, wherein each different first probe is a different address on the array apparatus;
providing a plurality of second biological probes, each second probe comprising a first region and a second region, each second probe being different from others in the plurality of second probes by comprising a different first region that is complementary to a different one of the first probes, the second region of each second probe being complementary to a specific target, such that each second probe addresses a complementary specific target from a different sample of the plurality of different samples being assayed to one of the different addresses on the array corresponding to a respective complementary different first probe;
assembling the target from each sample to the array with the plurality of second probes;
removing unassembled biological materials from the array; and
analyzing assay results comprising the step of determining the presence of the one target or the plurality of different targets in the plurality of different samples from whether the target from each different sample is assembled on the array at the corresponding first probe location. - View Dependent Claims (13, 14, 15, 16, 19, 20, 21, 22, 23, 27, 28)
incubating the plurality of different biological samples with the plurality of second probes to hybridize the biological targets per sample with complementary second regions of the second probes; and
incubating together the plurality of second probes with the plurality of first probes on the array apparatus to hybridize the first regions of the plurality of second probes to corresponding complementary first probes.
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14. The assay method of claim 12, wherein the step of removing comprises the step of washing any unhybridized second probes and any unhybridized targets off the array apparatus surface.
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15. The assay method of claim 12, wherein the plurality of different biological samples comprises the one target per sample to be multiplexed, wherein the second region of each second probe is the same and complementary to the one target per sample, and wherein the step of assembling comprises the steps of:
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separately preincubating a different second probe with each different sample of the plurality of different samples so that each different second probe hybrdizes to the complementary target from a respective sample, and incubating together the different hybridized second probes with the array apparatus to hybridize the different first regions of the different hybridized second probes with complementary first probes on the array corresponding to the different addresses.
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16. The assay method of claim 12, wherein the plurality of different biological samples comprises the plurality of different targets per sample to be multiplexed, wherein the second region of each second probe is different and complementary to a different one of the plurality of different targets per sample, and wherein the step of assembling comprises the steps of:
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separately preincubating different second probes with each different sample, the different second probes in a respective sample being complementary to the different targets of the respective sample so that each different second probe in the respective sample hybridizes to the complementary target of the respective sample, and incubating together the different hybridized second probes with the array apparatus to hybridize the different first regions of the different hybridized second probes with complementary first probes on the array corresponding to the different addresses.
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19. The assay method of claim 13, wherein each first probe and each complementary first region further comprises a member of a specific binding pair, and wherein the step of assembling further comprises the step of cross-linking the members of the pair.
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20. The assay method of claim 13, wherein the steps of incubating are performed simultaneously.
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21. The assay method of claim 13, wherein the step of incubating together the plurality of second probes with the plurality of first probes is performed before the step of incubating the different biological samples with the plurality of second probes.
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22. The assay method of multiplexing of claim 12, wherein the assay results are analyzed at a first location, the method further comprising communicating the assay results or a conclusion based on the assay results to a second location remote from the first location.
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23. The assay method of multiplexing of claim 22, wherein the one or more samples was obtained from a third location remote from the first location or the second location.
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27. The assay method of claim 12, wherein each first probe of the plurality of first probes comprises a first sequence of monomers, and wherein the first region of each second probe of the plurality of second probes comprises a second sequence of monomers, and wherein the first sequence of monomers comprises a first modified monomer and the second sequence of monomers comprises a second similarly modified monomer that is complementary to the first modified monomer, and wherein in the step of assembling, the first modified monomer preferentially hybridizes to the complementary second modified monomer instead of to a complementary monomer that is not similarly modified, such that the method provides specificity and sensitivity to the assay.
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28. The assay method of claim 12, wherein the plurality of first probes comprises oligonucleotide first probes and the first regions of the plurality of second probes comprises oligonucleotide regions,
wherein the oligonucleotide first probes comprise a plurality of first nucleotides having either a (3′ - →
5′
) or (5′
→
3′
) polarity, and a first modified nucleotide that has a reversed polarity with respect to the polarity of the plurality of first nucleotides, andwherein the oligonucleotide regions of the second probes comprise a plurality of second nucleotides having the same polarity as the polarity of the plurality of first nucleotides, the plurality of second nucleotides being complementary to the plurality of first nucleotides, and a second modified nucleotide that has a reversed polarity with respect to the polarity of the plurality of second nucleotides, the second reversed polarity nucleotide being complementary to the first reversed polarity nucleotide in the first probe, and wherein in the step of assembling, the plurality of first probes are hybridized to the plurality of second probes and the first reversed polarity nucleotide preferentially hybridizes to the complementary second reversed polarity nucleotide instead of to a complementary nucleotide whose polarity is not similarly reversed, such that the method provides specificity and sensitivity to the assay.
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17. An assay method of multiplexing on a single array one or more biological samples having one or more biological targets per sample, comprising the steps of:
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providing an array apparatus having a plurality of first biological probes on a substrate in an array pattern of features, each first probe being different, each different first probe being located on a different feature location of the array, wherein each different first probe is a different address on the array apparatus;
providing a plurality of second biological probes, each second probe comprising a first region and a second region, each second probe being different from others in the plurality of second probes by comprising a different first region that is complementary to a different one of the first probes, the second region of each second probe being complementary to a target from the one or more samples, such that each second probe addresses a target from a sample being assayed to one of the different addresses on the array corresponding to a respective complementary different first probe;
assembling the target from the sample to the array with the plurality of second probes;
removing unassembled biological materials from the array; and
analyzing assay results comprising the step of determining the presence of the one or more targets in the one or more samples from whether the target from the sample is assembled on the array at the corresponding first probe location, wherein each first probe comprises a first sequence of monomers, and wherein the first region of each second probe comprises a second sequence of monomers, and wherein the first sequence of monomers comprises a first modified monomer and the second sequence of monomers comprises a second similarly modified monomer that is complementary to the first modified monomer, and wherein in the step of assembling, the first modified monomer preferentially hybridizes to the complementary second modified monomer instead of to a complementary monomer that is not similarly modified, such that the method provides specificity and sensitivity to the assay.
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18. An assay method of multiplexing on a single array one or more biological samples having one or more biological targets per sample, comprising the steps of:
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providing an array apparatus having a plurality of first biological probes on a substrate in an array pattern of features, each first probe being different, each different first probe being located on a different feature location of the array, wherein each different first probe is a different address on the array apparatus;
providing a plurality of second biological probes, each second probe comprising a first region and a second region, each second probe being different from others in the plurality of second probes by comprising a different first region that is complementary to a different one of the first probes, the second region of each second probe being complementary to a target from the one or more samples, such that each second probe addresses a target from a sample being assayed to one of the different addresses on the array corresponding to a respective complementary different first probe;
assembling the target from the sample to the array with the plurality of second probes;
removing unassembled biological materials from the array; and
analyzing assay results comprising the step of determining the presence of the one or more targets in the one or more samples from whether the target from the sample is assembled on the array at the corresponding first probe location, wherein the plurality of first probes comprises oligonucleotide first probes and the first regions of the plurality of second probes comprises oligonucleotide regions, and wherein the oligonucleotide first probes comprise a plurality of first nucleotides having either a (3′
→
5′
) or (5′
→
3′
) polarity, and a first modified nucleotide that has a reversed polarity with respect to the polarity of the plurality of first nucleotides, andwherein the oligonucleotide regions of the second probes comprise a plurality of second nucleotides having the same polarity as the polarity of the plurality of first nucleotides, the plurality of second nucleotides being complementary to the plurality of first nucleotides, and a second modified nucleotide that has a reversed polarity with respect to the polarity of the plurality of second nucleotides, the second reversed polarity nucleotide being complementary to the first reversed polarity nucleotide in the first probe, and wherein in the step of assembling, the plurality of first probes are hybridized to the plurality of second probes and the first reversed polarity nucleotide preferentially hybridizes to the complementary second reversed polarity nucleotide instead of to a complementary nucleotide whose polarity is not similarly reversed, such that the method provides specificity and sensitivity to the assay.
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Specification
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Current AssigneeAgilent Technologies Europe BV (Agilent Technologies, Inc.)
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Original AssigneeAgilent Technologies, Inc.
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InventorsDelenstarr, Glenda C.
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Primary Examiner(s)Brusca, John S.
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Assistant Examiner(s)KIM, YOUNG J
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Application NumberUS09/436,437Time in Patent Office1,002 DaysField of Search435/6, 435/91.2US Class Current435/6.11CPC Class CodesC12Q 1/6837 using probe arrays or probe...C12Q 2523/101 Crosslinking agents, e.g. p...C12Q 2537/137 a displacement stepC12Q 2565/133 conformational analysisC12Q 2565/514 characterised by the use of...C40B 40/00 Libraries per se, e.g. arra...
