BaG, a new dimeric metalloproteinase/disintegrin from the Bothrops alternatus snake venom that interacts with alpha(5)beta(1) integrin

Author(s)

Cominetti, M. R. ^[1] ; Ribeiro, J. U. ; Fox, J. W. ; Selistre-de-Araujo, H. S.

Affiliation

^[1] Universidade Federal de São Carlos (UFSCAR). Centro de Ciências Biológicas e da Saúde - Brasil

• Document type: Journal article
• Source: Archives of Biochemistry and Biophysics; v. 416, n. 2, p. 171-179, Aug. 2003.
• Field of knowledge: Biological Sciences - Biochemistry

Abstract

The alpha(5)beta(1) integrin is one of the major fibronectin receptors which plays an essential role in the adhesion of normal and tumor cells to extracellular matrix. Here, we describe the isolation and characterization of a novel dimeric metalloproteinase/disintegrin, which is an inhibitor of fibronectin binding to the alpha(5)beta(1) integrin. This protein (BaG) was isolated from the venom of the South American snake Bothrops alternatus by gelatin-Sepharose affinity and anion exchange chromatography. The molecular mass of BaG was approximately 130 kDa under non-reducing conditions and 55 kDa under reducing conditions by SDS-PAGE. BaG shows proteolytic activity on casein that was inhibited by EDTA. 1,10-phenanthroline-treated BaG (BaG-I) inhibits ADP-induced platelet aggregation with an IC50 of 190 nM. BaG-I inhibits fibronectin-mediated K562 cell adhesion with an IC50 of 3.75 muM. K562 cells bind to BaG-I probably through interaction with alpha(5)beta(1) integrin, since anti-alpha(5)beta(1) antibodies inhibited K562 cell adhesion to BaG-I. In addition, BaG-I induces the detachment of K562 cells that were bound to fibronectin. In summary, we have purified a novel, dimeric snake venom metalloproteinase/disintegrin that binds to the alpha(5)beta(1) integrin. (AU)