| Literature DB >> 1694725 |
A M Pullen1, T Wade, P Marrack, J W Kappler.
Abstract
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.Mesh:
Substances:
Year: 1990 PMID: 1694725 DOI: 10.1016/0092-8674(90)90700-o
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582