Antigen detection using photocleavable labels
Provided herein are methods of using photocleavable labels for multiplex and serial antigen detection. The methods comprise detecting the presence of photocleavable labels, which are conjugated through functional linkers to antigen-binding complexes, which in turn non-covalently bind to antigens. The presence of a photocleavable label is indicative of the presence of an antigen specifically or selectively bound by an antigen-binding complex. Also provided are apparatuses for using photocleavable labels for multiplex and serial antigen detection.
1. A method for detecting the presence of an at least first antigen on or in a sample comprising a first antigen-binding complex capable of specifically binding the at least first antigen, the method comprising detecting the presence of a photocleavable label in the sample, wherein the photocleavable label is conjugated to the first antigen-binding complex through a functional linker, wherein the first antigen-binding complex is non-covalently bound to the at least first antigen forming an antigen-bound antigen-binding complex of formula (I):
wherein the presence of the photocleavable label is indicative of the presence of the at least first antigen; wherein the functional linker is an at least partially double-stranded oligonucleotide, wherein each oligonucleotide of the at least partially double-stranded oligonucleotide is 34 nucleotides in length and wherein the at least partially double-stranded oligonucleotide has a double-stranded section that is 28 nucleotides in length, wherein each oligonucleotide in the at least partially double-stranded oligonucleotide has a biotin on its 5′ end.
2. The method of claim 1 , further comprising photocleaving the photocleavable label.
3. The method of claim 2 , wherein photocleaving comprises exposing the sample to ultraviolet light.
4. The method of claim 1 , wherein the photocleavable label comprises a reporter moiety covalently bound to a photocleavable moiety.
5. The method of claim 4 , wherein the photocleavable moiety is selected from the group consisting of a 2-nitrobenzyl group, a benzoin group, a coumarinyl group, and a p-hydroxyphenacyl group.
6. The method of claim 5 , wherein the photocleavable moiety is a 2-nitrobenzyl group.
7. The method of claim 6 , wherein the 2-nitrobenzyl group comprises a substitution on the α-carbon and/or a 5-methoxy substitution on the benzene ring.
8. The method of claim 4 , wherein the reporter moiety is a colorimetric dye, a fluorescent dye, a radioactive label, a chemiluminescent group, or a bioluminescent group.
9. The method of claim 1 , wherein the sample is a tissue section, biopsy sample, cell culture sample, cell smear, or protein lysate.
10. The method of claim 1 , wherein each oligonucleotide in the at least partially double-stranded oligonucleotide has a photocleavable label on its 3′ end.
11. The method of claim 1 , wherein the first antigen-binding complex is defined by formula (II):
wherein the first antigen-binding complex comprises a primary antibody bound to a conjugation moiety, wherein the antigen-bound antigen-binding complex is further defined by formula (III):
12. The method of claim 11 , wherein the primary antibody is modified by at least one reducing agent.
13. The method of claim 11 , wherein the conjugation moiety is a heterobifunctional linker.
14. The method of claim 1 , wherein the first antigen-binding complex is defined by formula (IV):
wherein the first antigen-binding complex comprises a primary antibody covalently bound to a first ligand, wherein the first ligand is non-covalently bound to a first anti-ligand, wherein the antigen-bound antigen-binding complex is further defined by formula (V):
15. The method of claim 1 , wherein the first antigen-binding complex is defined by formula (VI):
wherein the first antigen-binding complex comprises a primary antibody covalently bound to a first ligand, wherein the first ligand is non-covalently bound to a first anti-ligand, wherein the second ligand is non-covalently bound to the first anti-ligand, wherein the antigen-bound antigen-binding complex is further defined by formula (VII):
16. The method of claim 1 , wherein the first antigen-binding complex is defined by formula (VIII):
wherein the first antigen-binding complex comprises a primary antibody bound by a secondary antibody, wherein the secondary antibody is covalently bound to a first ligand, wherein the first ligand is non-covalently bound to a first anti-ligand, wherein the antigen-bound antigen-binding complex is further defined by formula (IX):
17. The method of claim 1 , wherein the first antigen-binding complex is defined by formula (X):
wherein the first antigen-binding complex comprises a primary antibody bound by a secondary antibody, wherein the secondary antibody is covalently bound to a first ligand, wherein the first ligand is non-covalently bound to a first anti-ligand, wherein the second ligand is non-covalently bound to the first anti-ligand, wherein the antigen-bound antigen-binding complex is further defined by formula (XI):