Culurgioni Simone, Tang Minzhe, Hall David R, Walsh Martin A
Diamond Light Source, Harwell Science & Innovation Campus; Research Complex at Harwell, Harwell Science & Innovation Campus;
Diamond Light Source, Harwell Science & Innovation Campus; Research Complex at Harwell, Harwell Science & Innovation Campus.
J Vis Exp. 2017 Oct 2(128):56294. doi: 10.3791/56294.
Development of new antimicrobials and vaccines for Streptococcus pneumoniae (pneumococcus) are necessary to halt the rapid rise in multiple resistant strains. Carbohydrate substrate binding proteins (SBPs) represent viable targets for the development of protein-based vaccines and new antimicrobials because of their extracellular localization and the centrality of carbohydrate import for pneumococcal metabolism, respectively. Described here is a rationalized integrated protocol to carry out a comprehensive characterization of SP0092, which can be extended to other carbohydrate SBPs from the pneumococcus and other bacteria. This procedure can aid the structure-based design of inhibitors for this class of proteins. Presented in the first part of this manuscript are protocols for biochemical analysis by thermal shift assay, multi angle light scattering (MALS), and size exclusion chromatography (SEC), which optimize the stability and homogeneity of the sample directed to crystallization trials and so enhance the probability of success. The second part of this procedure describes the characterization of the SBP crystals using a tunable wavelength anomalous diffraction synchrotron beamline, and data collection protocols for measuring data that can be used to resolve the crystallized protein structure.
开发针对肺炎链球菌(肺炎球菌)的新型抗菌药物和疫苗对于遏制多重耐药菌株的迅速增加至关重要。碳水化合物底物结合蛋白(SBP)分别因其细胞外定位以及碳水化合物导入对肺炎球菌代谢的核心作用,成为基于蛋白质的疫苗和新型抗菌药物开发的可行靶点。本文描述了一种合理的综合方案,用于对SP0092进行全面表征,该方案可扩展至肺炎球菌和其他细菌的其他碳水化合物SBP。此程序有助于基于结构设计此类蛋白质的抑制剂。本手稿第一部分介绍了通过热迁移分析、多角度光散射(MALS)和尺寸排阻色谱(SEC)进行生化分析的方案,这些方案优化了用于结晶试验的样品的稳定性和均一性,从而提高成功的概率。此程序的第二部分描述了使用可调波长反常衍射同步加速器光束线对SBP晶体进行表征,以及用于测量可用于解析结晶蛋白质结构的数据的数据收集方案。