| Literature DB >> 2035841 |
J R Chagas1, L Juliano, E S Prado.
Abstract
Five intramolecularly quenched fluorogenic substrates for arginyl hydrolases with the sequence Abz-Phe-Arg-X-Y-EDDnp (X = Arg or Ser; Y = Val, Pro, or Arg) were synthesized by classical solution methods. Kinetics of their hydrolysis by tissue and plasma kallikreins, trypsin, and thrombin characterized Abz-Phe-Arg-Ser-Arg-EDDnp as a specific and sensitive substrate for the continuous assay of tissue kallikreins while Abz-Phe-Arg-Arg-Pro-EDDnp was the best substrate for human plasma kallikrein. The five peptides were poor substrates for trypsin and resistant to thrombin.Entities:
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Year: 1991 PMID: 2035841 DOI: 10.1016/0003-2697(91)90558-b
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365