Center for Inflammation, Translational and Clinical Lung Research, Temple University School of Medicine, 3500 N. Broad Street, Philadelphia, PA 19140, USA.
Toxins (Basel). 2013 Oct 22;5(10):1859-71. doi: 10.3390/toxins5101859.
The functional activity of superantigens is based on capacity of these microbial proteins to bind to both the β-chain of the T cell receptor (TcR) and the major histocompatibility complex (MHC) class II dimer. We have previously shown that a subset of the bacterial superantigens also binds to a membrane protein, designated p85, which is expressed by renal epithelial cells. This binding activity is a property of SEB, SEC1, 2 and 3, but not SEA, SED, SEE or TSST. The crystal structure of the tri-molecular complex of the superantigen staphylococcal enterotoxin B (SEB) with both the TcR and class II has previously been reported. However, the relative contributions of regions of the superantigen to the overall functional activity of this superantigen remain undefined. In an effort to better define the molecular basis for the interaction of SEB with the TcR β-chain, we report studies here which show the comparative contributions of amino- and carboxy-terminal regions in the superantigen activity of SEB. Recombinant fusion proteins composed of bacterial maltose-binding protein linked to either full-length or truncated toxins in which the 81 N-terminal, or 19 or 34 C-terminal amino acids were deleted, were generated for these studies. This approach provides a determination of the relative strength of the functional activity of the various regions of the superantigen protein.
超抗原的功能活性基于这些微生物蛋白与 T 细胞受体 (TcR) 的β链和主要组织相容性复合体 (MHC) Ⅱ类二聚体结合的能力。我们之前已经表明,一部分细菌超抗原也与一种膜蛋白结合,该蛋白被命名为 p85,其由肾上皮细胞表达。这种结合活性是 SEB、SEC1、2 和 3 的特性,但不是 SEA、SED、SEE 或 TSST 的特性。先前已经报道了三分子复合物超抗原金黄色葡萄球菌肠毒素 B (SEB) 与 TcR 和 II 类的晶体结构。然而,超抗原各区域对该超抗原整体功能活性的相对贡献仍未定义。为了更好地定义 SEB 与 TcR β 链相互作用的分子基础,我们在此报告了一些研究,这些研究表明氨基和羧基末端区域在 SEB 超抗原活性中的比较贡献。为了进行这些研究,生成了由细菌麦芽糖结合蛋白与全长或截短毒素连接而成的重组融合蛋白,其中删除了 81 个 N 端或 19 或 34 个 C 端氨基酸。这种方法提供了对超抗原蛋白各区域功能活性相对强度的测定。