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Plasma prekallikrein/kallikrein processing by lysosomal cysteine proteases.

作者信息

Barros Nilana M T, Puzer Luciano, Tersariol Ivarne L S, Oliva M Luiza V, Sampaio Claudio A M, Carmona Adriana K, Motta Guacyara da

机构信息

Departamento de Bioquímica, Universidade Federal de São Paulo/EPM, CEP 04044-020, São Paulo, SP, Brazil.

出版信息

Biol Chem. 2004 Nov;385(11):1087-91. doi: 10.1515/BC.2004.141.

Abstract

Plasma kallikrein plays a role in coagulation, fibrinolysis and inflammation. Cathepsins B and L participate in (patho)physiological processes such as peptide antigen processing, tissue remodeling events, protein turnover in cells, hormone processing and tumor invasion. The present work analyzes the processing of prekallikrein/kallikrein by lysosomal cathepsins. Prekallikrein is not hydrolyzed by catB, and catL generates an inactive fragment of prekallikrein. Both kallikrein chains are hydrolyzed by catL and the light chain is mainly hydrolyzed by catB; kallikrein activity is lower after incubation with catL compared to catB. Our data suggest that the plasma kallikrein/ kinin system can be controlled by cathepsins.

摘要

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