van Boxel Gijs I, Stewart-Jones Guillaume, Holmes Samantha, Sainsbury Sarah, Shepherd Dawn, Gillespie G M A, Harlos Karl, Stuart David I, Owens Ray, Jones E Yvonne
Cancer Research UK Receptor Structure Research Group, Division of Structural Biology, The Henry Wellcome Building for Genomic Medicine, Roosevelt Drive, Headington, Oxford OX3 7BN, UK.
J Immunol Methods. 2009 Oct 31;350(1-2):14-21. doi: 10.1016/j.jim.2009.08.008. Epub 2009 Aug 26.
T-cell receptors (TCRs) are membrane proteins which recognize antigens with high specificity forming the basis of the cellular immune response. The study of these receptors has been limited by the challenges in expressing sufficient quantities of stable soluble protein. Here we report our systematic approach for generating soluble, (alpha)(beta)-TCRs, for X-ray crystallographic studies. By using small-scale expression screens, novel standardized quality control mechanisms and crystallization and imaging robots we were able to add significantly to the current TCR structural database. Our success in crystallizing both isolated TCRs and Major histocompatibility complex (MHC):TCR complexes has provided us with sufficient data to develop focused crystallization screens, which have proved generically useful for the crystallization of this family of proteins and complexes.
T细胞受体(TCRs)是一种膜蛋白,能高度特异性地识别抗原,构成细胞免疫反应的基础。对这些受体的研究一直受到难以表达足够数量稳定可溶性蛋白这一挑战的限制。在此,我们报告了一种用于生成可溶性αβ-TCRs以进行X射线晶体学研究的系统方法。通过小规模表达筛选、新型标准化质量控制机制以及结晶和成像机器人,我们能够显著扩充当前的TCR结构数据库。我们成功地使分离的TCRs以及主要组织相容性复合体(MHC):TCR复合体结晶,这为我们提供了足够的数据来开发针对性的结晶筛选方法,事实证明这些方法对该蛋白家族及其复合体的结晶普遍有用。