Laboratório de Imunopatologia, Instituto Butantan, Butantã, São Paulo, SP, Brazil.
Toxicon. 2010 Jun 1;55(6):1093-9. doi: 10.1016/j.toxicon.2009.12.010. Epub 2010 Jan 6.
SVMPs are multi-domain proteolytic enzymes in which disintegrin-like and cysteine-rich domains bind to cell receptors, plasma or ECM proteins. We have recently reported that jararhagin, a P-III class SVMP, binds to collagen with high affinity through an epitope located within the Da-disintegrin sub-domain. In this study, we evaluated the binding of jararhagin to alpha(2)beta(1) integrin (collagen receptor) using monoclonal antibodies and recombinant jararhagin fragments. In solid phase assays, binding of jararhagin to alpha(2)beta(1) integrin was detectable from concentrations of 20 nM. Using recombinant fragments of jararhagin, only fragment JC76 (residues 344-421), showed a significant binding to recombinant alpha(2)beta(1) integrin. The anti-jararhagin monoclonal antibody MAJar 3 efficiently neutralised binding of jararhagin to collagen, but not to recombinant alpha(2)beta(1) integrin nor to cell-surface-exposed alpha(2)beta(1) integrin (alpha(2)-K562 transfected cells and platelets). The same antibody neutralised collagen-induced platelet aggregation. Our data suggest that jararhagin binding to collagen and alpha(2)beta(1) integrin occurs by two independent motifs, which are located on disintegrin-like and cysteine-rich domains, respectively. Moreover, toxin binding to collagen appears to be sufficient to inhibit collagen-induced platelet aggregation.
SVMPs 是一种具有多种结构域的蛋白水解酶,其中解体酶样和富含半胱氨酸的结构域与细胞受体、血浆或细胞外基质蛋白结合。我们最近报道称,属于 P-III 类 SVMP 的 Jararhagin 通过位于 Da-解体酶亚结构域内的一个表位与胶原蛋白具有高亲和力结合。在这项研究中,我们使用单克隆抗体和重组 Jararhagin 片段评估了 Jararhagin 与 α2β1 整合素(胶原蛋白受体)的结合。在固相测定中,Jararhagin 与 α2β1 整合素的结合可检测到 20 nM 的浓度。使用重组的 Jararhagin 片段,只有片段 JC76(残基 344-421)与重组 α2β1 整合素显示出明显的结合。抗 Jararhagin 单克隆抗体 MAJar 3 可有效中和 Jararhagin 与胶原蛋白的结合,但不能中和重组 α2β1 整合素或细胞表面暴露的 α2β1 整合素(α2-K562 转染细胞和血小板)。同样的抗体也能中和胶原蛋白诱导的血小板聚集。我们的数据表明,Jararhagin 与胶原蛋白和 α2β1 整合素的结合是通过两个独立的基序进行的,分别位于解体酶样和富含半胱氨酸的结构域上。此外,毒素与胶原蛋白的结合似乎足以抑制胶原蛋白诱导的血小板聚集。