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鉴定超抗原中毒性休克综合征毒素-1与II类主要组织相容性复合体分子的结合结构域。

Identification of binding domains on the superantigen, toxic shock syndrome-1, for class II MHC molecules.

作者信息

Soos J M, Russell J K, Jarpe M A, Pontzer C H, Johnson H M

机构信息

Department of Microbiology and Cell Science, University of Florida, Gainesville 32611.

出版信息

Biochem Biophys Res Commun. 1993 Mar 31;191(3):1211-7. doi: 10.1006/bbrc.1993.1346.

Abstract

Toxic shock syndrome toxin-1 (TSST-1) is a member of the staphylococcal enterotoxin superantigen family. In order to determine the regions on the TSST-1 molecule involved in binding to class II MHC, seven overlapping peptides of the entire TSST-1 molecule were synthesized and tested for their ability to compete with 125I-TSST-1 for binding to class II MHC on murine A20 cells and HLA on Raji cells. Peptides corresponding to N-terminal amino acid residues 39 through 68 and C-terminal residues 155 through 194 competed with 125I-TSST-1 for binding to class II MHC. Also, binding studies with class II MHC beta-chain peptides indicate that regions encompassed by I-A beta b(30-60) and I-A beta b(60-90) are binding regions for TSST-1. Thus, we have identified binding domains on the TSST-1 molecule for class II MHC molecule receptors on antigen presenting cells.

摘要

中毒性休克综合征毒素-1(TSST-1)是葡萄球菌肠毒素超抗原家族的成员。为了确定TSST-1分子上与II类主要组织相容性复合体(MHC)结合的区域,合成了整个TSST-1分子的七个重叠肽,并测试了它们与125I-TSST-1竞争结合小鼠A20细胞上的II类MHC和Raji细胞上的人白细胞抗原(HLA)的能力。对应于N端氨基酸残基39至68和C端残基155至194的肽与125I-TSST-1竞争结合II类MHC。此外,与II类MHCβ链肽的结合研究表明,I-Aβb(30-60)和I-Aβb(60-90)所涵盖的区域是TSST-1的结合区域。因此,我们已经确定了TSST-1分子上抗原呈递细胞上II类MHC分子受体的结合域。

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