Ohmura T, Sakata A, Onoue K
Department of Immunology, Kumamoto University School of Medicine, Japan.
J Exp Med. 1992 Sep 1;176(3):887-91. doi: 10.1084/jem.176.3.887.
The identity of the guanine nucleotide-binding protein (G protein) involved in T cell activation pathways remains unclear. We identified a 68-kD GTP-binding protein associated with the T cell receptor (TCR)/CD3 complex using immunoprecipitation and GTP-affinity labeling techniques. Proteins coimmunoprecipitated with the TCR/CD3 complex in digitonin lysate of a human leukemic T cell line, MOLT 16, were incubated with alpha-[32P]GTP and irradiated with ultraviolet rays to covalently link the labeled GTP to GTP-binding proteins. They were then analyzed by electrophoresis. The 68-kD protein exhibited nucleotide specificity for GTP-binding and was insensitive to cholera and pertussis toxins. The 68-kD GTP-binding protein could be coimmunoprecipitated with the TCR/CD3 complex but not with other surface molecules such as major histocompatibility complex class I and lymphocyte function associated-1, which do not cause rapid Ca2+ mobilization. These suggest that the 68-kD GTP-binding protein is specifically associated with the TCR/CD3 complex.
参与T细胞激活途径的鸟嘌呤核苷酸结合蛋白(G蛋白)的身份仍不清楚。我们使用免疫沉淀和GTP亲和标记技术,鉴定了一种与T细胞受体(TCR)/CD3复合物相关的68-kD GTP结合蛋白。将在人白血病T细胞系MOLT 16的洋地黄皂苷裂解物中与TCR/CD3复合物共免疫沉淀的蛋白质,与α-[32P]GTP一起孵育,并用紫外线照射,以使标记的GTP与GTP结合蛋白共价连接。然后通过电泳对它们进行分析。该68-kD蛋白对GTP结合表现出核苷酸特异性,并且对霍乱毒素和百日咳毒素不敏感。68-kD GTP结合蛋白可以与TCR/CD3复合物共免疫沉淀,但不能与其他不会引起快速Ca2+动员的表面分子(如主要组织相容性复合体I类和淋巴细胞功能相关抗原1)共免疫沉淀。这些结果表明,68-kD GTP结合蛋白与TCR/CD3复合物特异性相关。