Hybridization chain reaction amplification for in situ imaging
The present invention relates to the use of fluorescently labeled nucleic acid probes to identify and image analytes in a biological sample. In the preferred embodiments, a probe is provided that comprises a target region able to specifically bind an analyte of interest and an initiator region that is able to initiate polymerization of nucleic acid monomers. After contacting a sample with the probe, labeled monomers are provided that form a tethered polymer. Triggered probes and self-quenching monomers can be used to provide active background suppression.
1. A method for detecting an analyte in a biological sample, the method comprising:
contacting the sample with a probe comprising a target region and an initiation nucleic acid region, wherein the target region is able to specifically bind to the analyte;
contacting the sample with a first metastable monomer comprising a hairpin loop region and an initiator complement region that comprises a first sticky end and is complementary to the initiation nucleic acid region of the probe; and
contacting the sample with a second metastable monomer comprising a second sticky end that is complementary to the hairpin loop region of the first monomer,
wherein the first monomer is labeled with a first fluorophore; and
detecting the analyte in the sample by measuring fluorescence of the sample.
2. The method of claim 1 , wherein the analyte is a nucleic acid.
3. The method of claim 2 , wherein the analyte is a gene.
4. The method of claim 3 , wherein the analyte is mRNA.
5. The method of claim 3 , wherein the target region is complementary to a portion of the nucleic acid.
6. The method of claim 5 , wherein the initiation region is complementary to a portion of the analyte binding region.
7. The method of claim 1 , wherein the second monomer is labeled with a second fluorophore.
8. The method of claim 7 , wherein the first and second fluorophore are different.
9. The method of claim 1 , wherein the first monomer comprises a fluorescence quencher.
10. The method of claim 1 , wherein the target region comprises an antibody.
11. The method of claim 1 , wherein the probe undergoes a conformational change upon biding of the target region to the analyte, and wherein the conformation change makes the initiation region available to bind to the first monomer.
12. The method of claim 1 , wherein the first and second metastable monomers are hairpin monomers.
13. The method of claim 1 , additionally comprising contacting the sample with a third and fourth metastable monomer.
14. A method of in situ imaging comprising:
contacting a biological sample with a probe comprising a target region capable of specifically binding an analyte of interest and an initiator region, such that the probe binds to the analyte of interest;
contacting the biological sample with a first fluorescently labeled metastable monomer comprising a hairpin loop region and an initiator complement region that comprises a first sticky end that hybridizes to the initiator region of the probe; and
contacting the sample with a second fluorescently labeled metastable monomer comprising a second sticky end that is complementary to the hairpin loop region of the first monomer such that the monomers form a fluorescently labeled polymer tethered to the analyte; and
detecting the fluorescently labeled polymer.
15. The method of claim 14 , wherein the fluorescent label, on at least one of the monomers is quenched prior to formation of the tethered polymer.
16. The method of claim 14 , wherein the probe is a triggered probe.
17. The method of claim 16 , wherein the initiator region of the triggered probe only becomes available to hybridize to the first monomer when the target region of the probe is bound to the analyte of interest.
18. The method of claim 14 , wherein the sample is washed to remove unbound probe prior to contacting with the fluorescently labeled monomers.