Günther Sebastian, Varma Ashok K, Moza Beenu, Kasper Katherine J, Wyatt Aaron W, Zhu Penny, Rahman A K M Nur-ur, Li Yili, Mariuzza Roy A, McCormick John K, Sundberg Eric J
Boston Biomedical Research Institute, Watertown, MA 02472, USA.
J Mol Biol. 2007 Aug 3;371(1):210-21. doi: 10.1016/j.jmb.2007.05.038. Epub 2007 May 18.
Superantigens (SAGs) interact with host immune receptors to induce a massive release of inflammatory cytokines that can lead to toxic shock syndrome and death. Bacterial SAGs can be classified into five distinct evolutionary groups. Group V SAGs are characterized by the alpha3-beta8 loop, a unique approximately 15 amino acid residue extension that is required for optimal T cell activation. Here, we report the X-ray crystal structures of the group V SAG staphylococcal enterotoxin K (SEK) alone and in complex with the TCR hVbeta5.1 domain. SEK adopts a unique TCR binding orientation relative to other SAG-TCR complexes, which results in the alpha3-beta8 loop contacting the apical loop of framework region 4, thereby extending the known TCR recognition site of SAGs. These interactions are absolutely required for TCR binding and T cell activation by SEK, and dictate the TCR Vbeta domain specificity of SEK and other group V SAGs.
超抗原(SAGs)与宿主免疫受体相互作用,诱导炎性细胞因子大量释放,进而可能导致中毒性休克综合征和死亡。细菌超抗原可分为五个不同的进化组。第五组超抗原的特征是α3-β8环,这是一个独特的约15个氨基酸残基的延伸部分,是最佳T细胞激活所必需的。在此,我们报告了第五组超抗原葡萄球菌肠毒素K(SEK)单独以及与TCR hVβ5.1结构域形成复合物时的X射线晶体结构。与其他超抗原-TCR复合物相比,SEK采用了独特的TCR结合方向,这导致α3-β8环与构架区4的顶端环接触,从而扩展了已知的超抗原TCR识别位点。这些相互作用是SEK与TCR结合及T细胞激活所绝对必需的,并决定了SEK和其他第五组超抗原的TCR Vβ结构域特异性。