Photoaffinity labeling is a chemoproteomics technique used to attach "labels" to the active site of a large molecule, especially a protein. The "label" attaches to the molecule loosely and reversibly, and has an inactive site which can be converted using photolysis into a highly reactive form, which causes the label to bind more permanently to the large molecule via a covalent bond.[1][2] The technique was first described in the 1970s.[3] Molecules that have been used as labels in this process are often analogs of complex molecules, in which certain functional groups are replaced with a photoreactive group, such as an azide, a diazirine or a benzophenone.[4][5][6]
References
edit- ^ Photoaffinity labeling
- ^ Photoaffinity labeling, Gold Book
- ^ Ruoho, A. E.; Kiefer, H.; Roeder, P. E.; Singer, S. J. (1973). "The mechanism of photoaffinity labeling". Proceedings of the National Academy of Sciences of the United States of America. 70 (9): 2567–2571. Bibcode:1973PNAS...70.2567R. doi:10.1073/pnas.70.9.2567. PMC 427057. PMID 4517671.2567-2571&rft.date=1973&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC427057#id-name=PMC&rft_id=info:pmid/4517671&rft_id=info:doi/10.1073/pnas.70.9.2567&rft_id=info:bibcode/1973PNAS...70.2567R&rft.aulast=Ruoho&rft.aufirst=A. E.&rft.au=Kiefer, H.&rft.au=Roeder, P. E.&rft.au=Singer, S. J.&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC427057&rfr_id=info:sid/en.wikipedia.org:Photoaffinity labeling" class="Z3988">
- ^ Bush, J. T.; Walport, L. J.; McGouran, J. F.; Leung, I. K. H.; Berridge, G. (2013). "The Ugi four-component reaction enables expedient synthesis and comparison of photoaffinity probes". Chemical Science. 4 (12): 4115–4120. doi:10.1039/C3SC51708J.4115-4120&rft.date=2013&rft_id=info:doi/10.1039/C3SC51708J&rft.aulast=Bush&rft.aufirst=J. T.&rft.au=Walport, L. J.&rft.au=McGouran, J. F.&rft.au=Leung, I. K. H.&rft.au=Berridge, G.&rft_id=https://doi.org/10.1039%2FC3SC51708J&rfr_id=info:sid/en.wikipedia.org:Photoaffinity labeling" class="Z3988">
- ^ Panov, M. S.; Voskresenska, V. D.; Ryazantsev, M. N.; Tarnovsky, A. N.; Wilson, R. M. (2013). "5-Azido-2-aminopyridine, a New Nitrene/Nitrenium Ion Photoaffinity Labeling Agent That Exhibits Reversible Intersystem Crossing between Singlet and Triplet Nitrenes". Journal of the American Chemical Society. 135 (51): 19167–19179. Bibcode:2013JAChS.13519167P. doi:10.1021/ja405637b. PMID 24219134.19167-19179&rft.date=2013&rft_id=info:pmid/24219134&rft_id=info:doi/10.1021/ja405637b&rft_id=info:bibcode/2013JAChS.13519167P&rft.aulast=Panov&rft.aufirst=M. S.&rft.au=Voskresenska, V. D.&rft.au=Ryazantsev, M. N.&rft.au=Tarnovsky, A. N.&rft.au=Wilson, R. M.&rft_id=https://scholarworks.bgsu.edu/chem_pub/182&rfr_id=info:sid/en.wikipedia.org:Photoaffinity labeling" class="Z3988">
- ^ Akiyama, S.; Cornwell, M. M.; Kuwano, M.; Pastan, I.; Gottesman, M. M. (1988). "Most drugs that reverse multidrug resistance also inhibit photoaffinity labeling of P-glycoprotein by a vinblastine analog". Molecular Pharmacology. 33 (2): 144–147. PMID 2893251.144-147&rft.date=1988&rft_id=info:pmid/2893251&rft.aulast=Akiyama&rft.aufirst=S.&rft.au=Cornwell, M. M.&rft.au=Kuwano, M.&rft.au=Pastan, I.&rft.au=Gottesman, M. M.&rfr_id=info:sid/en.wikipedia.org:Photoaffinity labeling" class="Z3988">