Photoaffinity reagents for use with pepsin and other carboxyl proteases.
S H Hixson, J L Hurwitz, K J Langridge, D C Nichols, K M Provost, A M Wolff
Index: Biochem. Biophys. Res. Commun. 111(2) , 630-5, (1983)
Full Text: HTML
Abstract
Two compounds have been designed to serve as photoaffinity reagents for use with carboxyl proteases. 1,2-Epoxy-3-(4'-azido-2'-nitrophenoxy)propane has been synthesized and shown to react with porcine pepsin in the same fashion as the traditional inhibitor 1,2-epoxy-3-(p-nitrophenoxy)propane, while p-azidophenacyl bromide is similar to other phenacyl bromides in its reaction with pepsin. In combination with p-azido-alpha-diazoacetophenone, previously shown to resemble alpha-diazo carbonyl reagents in its reaction with pepsin, photoaffinity analogs are now available for all three of the widely-used carboxyl protease inhibitors.
Related Compounds
Related Articles:
2015-01-01
[Sci. Rep. 5 , 10144, (2015)]
2013-04-01
[Nucleic Acids Res. 41(8) , 4565-72, (2013)]
2009-01-01
[PLoS ONE 4(12) , e8143, (2009)]
1987-06-01
[J. Bacteriol. 169(6) , 2659-66, (1987)]
1984-01-05
[J. Mol. Biol. 172(1) , 77-86, (1984)]