Isolation and Characterization of EMS16, a C-Lectin Type Protein from Echis multisquamatus Venom, a Potent and Selective Inhibitor of the α2β1 Integrin

We have isolated and characterized EMS16, a potent and selective inhibitor of the α2β1 integrin, from Echis multisquamatus venom. It belongs to the family of C-lectin type of proteins (CLPs), and its amino acid sequence is homologous with other members of this protein family occurring in snake venom...

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Published inBiochemistry (Easton) Vol. 39; no. 32; pp. 9859 - 9867
Main Authors Marcinkiewicz, Cezary, Lobb, Roy R, Marcinkiewicz, Mariola M, Daniel, James L, Smith, J. Bryan, Dangelmaier, Carol, Weinreb, Paul H, Beacham, Dorothy A, Niewiarowski, Stefan
Format Journal Article
LanguageEnglish
Published American Chemical Society 15.08.2000
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Summary:We have isolated and characterized EMS16, a potent and selective inhibitor of the α2β1 integrin, from Echis multisquamatus venom. It belongs to the family of C-lectin type of proteins (CLPs), and its amino acid sequence is homologous with other members of this protein family occurring in snake venoms. EMS16 (M r ∼ 33K) is a heterodimer composed of two distinct subunits linked by S−S bonds. K562 cells transfected with α2 integrin selectively adhere to immobilized EMS16, but not to two other snake venom-derived CLPs, echicetin and alboaggregin B. EMS16 inhibits adhesion of α2β1-expressing cells to immobilized collagen I at picomolar concentrations, and the platelet/collagen I interaction in solution at nanomolar concentrations. EMS16 inhibits binding of isolated, recombinant I domain of α2 integrin to collagen in an ELISA assay, but not the interaction of isolated I domain of α1 integrin with collagen IV. Studies with monoclonal antibodies suggested that EMS16 binds to the α2 subunit of the integrin. EMS16 inhibits collagen-induced platelet aggregation, but has no effect on aggregation induced by other agonists such as ADP, thromboxane analogue (U46619), TRAP, or convulxin. EMS16 also inhibits collagen-induced, but not convulxin-induced, platelet cytosolic Ca2+ mobilization. In addition, EMS16 inhibits HUVEC migration in collagen I gel. In conclusion, we report a new, potent viper venom-derived inhibitor of α2β1 integrin, which does not belong to the disintegrin family.
Bibliography:Aided in part by an Initial Investigatorship from the American Heart Association South-Eastern Pennsylvania Chapter (C.M.), W. W. Smith Charitable Trust Research Grant (C.M.), NIH FIRST award (D.A.B.), American Heart Association (D.A.B. and S.N.), American Diabetes Association (S.N.), and Barra Foundation (S.N.).
istex:4E5432BD345795208CF8C82E571AC639161CB43C
ark:/67375/TPS-M7MGQ6L4-3
ISSN:0006-2960
1520-4995
DOI:10.1021/bi000428a