Pullen A M, Wade T, Marrack P, Kappler J W
Howard Hughes Medical Institute, Department of Medicine, National Jewish Center for Immunology and Respiratory Medicine, Denver, Colorado 80206.
Cell. 1990 Jun 29;61(7):1365-74. doi: 10.1016/0092-8674(90)90700-o.
Superantigen-MHC complexes are known to stimulate T cells primarily via the V beta element of the T cell receptor. In this paper we identify a number of amino acid residues that define the region of a particular V beta element interacting with one of the self-superantigens, MIs-1a. These residues are predicted to lie on a beta-pleated sheet of the T cell receptor, away from the complementarity determining regions of the receptor, which are thought to interact with complexes of conventional peptide antigens and MHC. In support of this prediction, mutations affecting MIs-1a activity have no effect on the response to conventional antigen and MHC.
已知超抗原-MHC复合物主要通过T细胞受体的Vβ元件刺激T细胞。在本文中,我们确定了一些氨基酸残基,这些残基定义了特定Vβ元件与一种自身超抗原MIs-1a相互作用的区域。预计这些残基位于T细胞受体的β折叠片上,远离受体的互补决定区,而互补决定区被认为与传统肽抗原和MHC的复合物相互作用。支持这一预测的是,影响MIs-1a活性的突变对传统抗原和MHC的反应没有影响。