Studies on synthetic peptide substrates for F XII enzymes.

Abstract:

:Screening of chromogenic peptide substrates have shown that FXIIa readily splits substrates of D-Pro-Phe-Arg-pNA (S-2302) and -Gly-Arg-pNA (e.g. S-2222) types. The latter type is preferred in a system where kallikrein is present. By using the substrate S-2222 a method for the determination of beta FXIIa inhibitors has been designed. Chromatography data show that C1-esterase inhibitor is the major inhibitor of beta FXIIa in plasma. Preliminary studies have also been performed on the assay of FXII in human plasma. The procedure to obtain a complete activation of FXII has still to be studied.

journal_name

Adv Exp Med Biol

authors

Friberger P,Aurell L,Rees W,Gallimore MJ

doi

10.1007/978-1-4757-0154-8_7

subject

Has Abstract

pub_date

1986-01-01 00:00:00

pages

53-61

eissn

0065-2598

issn

2214-8019

journal_volume

198 Pt B

pub_type

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