INTEGRATION OF A PROTEIN COLOCALIZATION DEVICE (PCD) ONTO A MICROFLUIDIC DEVICE
Provided herein are structures and methods for detecting one or more analyte molecules present in a sample. In some embodiments, the one or more analyte molecules are detected using one or more supramolecular structures. In some embodiments, the supramolecular structures are bi-stable, wherein the supramolecular structures shift from an unstable state to a stable state through interaction with one or more analyte molecules from the sample. In some embodiments, the stable state supramolecular structures are configured to provide a signal for analyte molecule detection and quantification.
1 . A method for generating analyte capture data, the method comprising:
attaching a plurality of supramolecular structures to a surface of a substrate, wherein the supramolecular structures each comprise one or more affinity binders attached to a core structure;
exposing the surface to a sample comprising an analyte;
interrogating the surface to identify one or more capture sites of bound analytes; and
comparing the capture sites to a decode mapping file to generate qualitative or quantitative analyte capture data.
2 . The method of claim 1 , wherein the core structure comprises a DNA origami.
3 . The method of claim 1 , wherein the substrate comprises a flow cell or a portion of a flow-cell.
4 . The method of claim 1 , wherein the affinity binders comprise one or more of a protein, a peptide, an antibody, an aptamer, a fluorophore, a darpin, a catalyst, a polymerization initiator, a polymer, or combinations thereof.
5 . The method of claim 1 , further comprising incubating the surface and the sample.
6 . The method of claim 1 , wherein the decode mapping file comprises location data relating placement of supramolecular structures and associated affinity binders on the surface.
7 . A method for generating analyte capture data, the method comprising:
attaching a plurality of supramolecular structures to a surface of a substrate, wherein the supramolecular structures each comprise one or more affinity binders attached to a core structure;
generating a decode mapping file for the surface, wherein decode mapping file comprises location data relating placement of supramolecular structures and associated affinity binders on the surface; and
comparing one or more capture sites of one or more analytes on the surface after exposure to a sample to the decode mapping file to generate qualitative or quantitative analyte capture data.
8 . The method of claim 7 , wherein the core structure comprises a DNA origami.
9 . The method of claim 7 , wherein the substrate comprises a flow cell or a portion of a flow-cell.
10 . The method of claim 7 , wherein the affinity binders comprise one or more of a protein, a peptide, an antibody, an aptamer, a fluorophore, a darpin, a catalyst, a polymerization initiator, a polymer, or combinations thereof.
11 . A method for generating analyte capture data, the method comprising:
attaching a plurality of supramolecular structures to a surface of a substrate, wherein the supramolecular structures each comprise one or more affinity binders attached to a core structure;
exposing the surface to a sample comprising one or more analytes; and
determining which analyte was captured at each capture site on the surface to generate qualitative or quantitative analyte capture data.
12 . The method of claim 11 , wherein the core structure comprises a DNA origami.
13 . The method of claim 11 , wherein the substrate comprises a flow cell or a portion of a flow-cell.
14 . The method of claim 11 , wherein the affinity binders comprise one or more of a protein, a peptide, an antibody, an aptamer, a fluorophore, a darpin, a catalyst, a polymerization initiator, a polymer, or combinations thereof.
15 . The method of claim 11 , further comprising incubating the surface and the sample.
16 . A method for generating analyte capture data, the method comprising:
exposing, in a solution, a plurality of supramolecular structures to a sample comprising one or more analytes, wherein the supramolecular structures each comprise one or more affinity binders attached to a core structure;
processing the solution to remove supramolecular structures that have not bound analyte;
deconstructing complexes of the supramolecular structure and analyte present in the solution to release one or more unique identifiers associated with each binding event of analyte to a respective supramolecular structure;
isolating the one or more unique identifiers in the solution;
exposing a surface seeded with a one or more adapter types to the solution comprising the one or more unique identifiers; and
performing a readout operation of the one or more unique identifiers which have interacted with the one or more adapters to generate qualitative or quantitative analyte capture data.
17 . The method of claim 16 , further comprising incubating the supramolecular structures and the sample in solution.
18 . The method of claim 16 , wherein the one or more unique identifiers comprise barcode sequences.
19 . The method of claim 16 , wherein the one or more adapter types comprise one or more primers, wherein at least a subset of the one or more primers are complementary to at least a portion of the one or more unique identifiers.
20 . The method of claim 16 , wherein the core structure comprises a DNA origami.
21 . The method of claim 16 , wherein the surface is provided as a portion of a flow cell.
22 . The method of claim 16 , wherein the affinity binders comprise one or more of a protein, a peptide, an antibody, an aptamer, a fluorophore, a darpin, a catalyst, a polymerization initiator, a polymer, or combinations thereof.
23 . A method for generating analyte capture data, the method comprising:
exposing, in a solution, a plurality of supramolecular structures to a sample comprising one or more analytes, wherein the supramolecular structures each comprise one or more affinity binders attached to a core structure;
processing the solution to remove supramolecular structures that have bound analyte;
deconstructing supramolecular structures unbound to analytes and remaining in the solution to release one or more unique identifiers indicative of which analyte or analytes to which the remaining supramolecular structures have an affinity;
isolating the one or more unique identifiers in the solution;
exposing a surface seeded with a one or more adapter types to the solution comprising the one or more unique identifiers; and
performing a readout operation of the one or more unique identifiers which have interacted with the one or more adapters to generate qualitative or quantitative analyte capture data.
24 . A substrate comprising a plurality of supramolecular structures, each supramolecular structure comprising:
a core structure comprising a plurality of core molecules;
one or more capture molecules linked to the supramolecular core at a first set of locations;
one or more detector molecules linked to the supramolecular core at a second set of locations; and
one or more barcode sequences linked to the supramolecular core at locations other than the first set of locations and the second set of locations, wherein the one or more barcode sequences identify the core structure, the capture molecules, the detector molecules, or combinations thereof;
wherein one or both of the capture molecules or the detector molecules selectively bind to an analyte of interest.
25 . The substrate of claim 24 , wherein the barcode sequences comprise nucleic acid sequences.
26 . The substrate of claim 24 , wherein each core structure of the plurality of supramolecular structures is identical to each other.
27 . The substrate of claim 24 , wherein the substrate comprises a solid support, solid substrate, a polymer matrix, or a molecular condensate.
28 . The substrate of claim 24 , wherein the analyte of interest comprises a protein, a peptide, a peptide fragment, a lipid, a DNA, a RNA, an organic molecule, an inorganic molecule, complexes thereof, or any combinations thereof.
29 . The substrate of claim 24 , wherein each supramolecular structure is a nanostructure.
30 . The substrate of claim 24 , wherein the plurality of core molecules for each core structure comprises one or more nucleic acid strands, one or more branched nucleic acids, one or more peptides, one or more small molecules, or combinations thereof.
31 . The substrate of claim 24 , wherein each core structure independently comprises a scaffolded deoxyribonucleic acid (DNA) origami, a scaffolded ribonucleic acid (RNA) origami, a scaffolded hybrid DNA:RNA origami, a single-stranded DNA tile structure, a multi-stranded DNA tile structure, a single-stranded RNA origami, a multi-stranded RNA tile structure, hierarchically composed DNA or RNA origami with multiple scaffolds, a peptide structure, or combinations thereof.
32 . The substrate of claim 24 , wherein the one or more capture molecules and one or more detector molecules for each supramolecular structure independently comprise a protein, a peptide, an antibody, an aptamer (RNA and DNA), a fluorophore, a darpin, a catalyst, a polymerization initiator, a polymer, or combinations thereof.