Centro de Biotecnologia, Instituto Butantan, São Paulo, Brazil; Programa de Pós-Graduação Interunidades em Biotecnologia, Instituto de Ciências Biomédicas, e Laboratório de Zoonoses Bacterianas do Veterinária Preventiva e Saúde Animal, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, São Paulo, Brazil.
Am J Trop Med Hyg. 2013 Dec;89(6):1103-16. doi: 10.4269/ajtmh.13-0205. Epub 2013 Aug 19.
We report cloning, expression, purification, and characterization of three predicted leptospiral membrane proteins (LIC11360, LIC11009, and LIC11975). In silico analysis and proteinase K accessibility data suggest that these proteins might be surface exposed. We show that proteins encoded by LIC11360, LIC11009 and LIC11975 genes interact with laminin in a dose-dependent and saturable manner. The proteins are referred to as leptospiral surface adhesions 23, 26, and 36 (Lsa23, Lsa26, and Lsa36), respectively. These proteins also bind plasminogen and generate active plasmin. Attachment of Lsa23 and Lsa36 to fibronectin occurs through the involvement of the 30-kDa and 70-kDa heparin-binding domains of the ligand. Dose-dependent, specific-binding of Lsa23 to the complement regulator C4BP and to a lesser extent, to factor H, suggests that this protein may interfere with the complement cascade pathways. Leptospira spp. may use these interactions as possible mechanisms during the establishment of infection.
我们报告了三种预测的钩端螺旋体膜蛋白(LIC11360、LIC11009 和 LIC11975)的克隆、表达、纯化和特性。计算机分析和蛋白水解酶可及性数据表明,这些蛋白可能是表面暴露的。我们表明,由 LIC11360、LIC11009 和 LIC11975 基因编码的蛋白以剂量依赖和饱和的方式与层粘连蛋白相互作用。这些蛋白分别被称为钩端螺旋体表面黏附素 23、26 和 36(Lsa23、Lsa26 和 Lsa36)。这些蛋白还结合纤维蛋白溶酶原并产生活性纤维蛋白溶酶。Lsa23 和 Lsa36 与纤维连接蛋白的附着是通过配体的 30kDa 和 70kDa 肝素结合结构域的参与来实现的。Lsa23 与补体调节剂 C4BP 的剂量依赖性特异性结合,并且在较小程度上与因子 H 结合,表明该蛋白可能干扰补体级联途径。钩端螺旋体属可能在感染的建立过程中利用这些相互作用作为可能的机制。