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Bioorg Med Chem Lett ; 23(6): 1608-11, 2013 Mar 15.
Article in English | MEDLINE | ID: mdl-23414805

ABSTRACT

Irreversible modification is one of the most promising strategies to identify cellular receptors of bioactive small molecules. Here we report that receptor proteins can be chemically tagged using a 5-sulfonyl tetrazole probe. 5-Sulfonyl tetrazole easily accepted nucleophilic attack of thiol groups, while 5-sulfinyl tetrazole did not. These functional groups were introduced into probe molecules of a natural product. Cyclosporine A, an immunosuppressant produced by a microbe, was derivatized to possess 5-sulfonyl tetrazole and a tag group, which enabled chemical tagging of cyclophilin A, the cellular receptor of cyclosporine A. Cyclosporine A derivative possessing 5-sulfinyl tetrazole could not tag cyclophilin A. This technique will allow efficient identification of cellular receptors of bioactive small molecules.


Subject(s)
Cyclophilin A/chemistry , Cyclosporine/chemistry , Tetrazoles/chemistry , Cyclophilin A/metabolism , Cyclosporine/metabolism , Ligands , Protein Binding
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