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微生物超抗原葡萄球菌肠毒素A的T细胞抗原受体结合位点。

T-cell antigen receptor binding sites for the microbial superantigen staphylococcal enterotoxin A.

作者信息

Pontzer C H, Irwin M J, Gascoigne N R, Johnson H M

机构信息

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

出版信息

Proc Natl Acad Sci U S A. 1992 Aug 15;89(16):7727-31. doi: 10.1073/pnas.89.16.7727.

Abstract

We have examined the interaction of the microbial superantigen staphylococcal enterotoxin A (SEA) with peptides corresponding to overlapping regions of the T-cell antigen receptor beta chain variable region V beta 3. SEA is known to stimulate murine T cells bearing certain V beta elements, among them V beta 3. Five peptides were synthesized representing amino acids 1-24, 20-44, 39-60, 57-77, and 74-95 of V beta 3. We demonstrate here that soluble V beta 3-bearing beta chains can bind to a complex of SEA and major histocompatibility complex class II and that the synthetic peptide V beta 3-(57-77) blocked this interaction. The peptide V beta 3-(57-77) also inhibited SEA-induced interferon-gamma production and SEA-induced proliferation of B10.BR spleen cells. Conversely, the peptide corresponding to amino acids 57-77 of V beta 8.2, a V beta element that is not recognized by SEA, decreased staphylococcal enterotoxin C-2-induced proliferation but did not affect SEA-induced proliferation. The peptide inhibition of SEA-induced function was due at least in part to inhibition of V beta 3-bearing T-cell activity, since the percentage of T cells reactive with an anti-V beta 3 monoclonal antibody was significantly reduced by V beta 3-(57-77). These data suggest that the region of V beta 3 encompassing amino acids 57-77 is an area that displays the appropriate sequence and conformation for binding of the SEA molecule and blocking of the resultant interaction with the T-cell antigen receptor.

摘要

我们研究了微生物超抗原葡萄球菌肠毒素A(SEA)与T细胞抗原受体β链可变区Vβ3重叠区域对应的肽段之间的相互作用。已知SEA可刺激带有某些Vβ元件的小鼠T细胞,其中包括Vβ3。合成了代表Vβ3的第1 - 24、20 - 44、39 - 60、57 - 77和74 - 95位氨基酸的五种肽段。我们在此证明,可溶性携带Vβ3的β链可与SEA和主要组织相容性复合体II类分子的复合物结合,并且合成肽Vβ3 -(57 - 77)可阻断这种相互作用。肽段Vβ3 -(57 - 77)还抑制SEA诱导的干扰素-γ产生以及SEA诱导的B10.BR脾细胞增殖。相反,对应于Vβ8.2的第57 - 77位氨基酸的肽段(SEA不识别的一种Vβ元件)可降低葡萄球菌肠毒素C - 2诱导的增殖,但不影响SEA诱导的增殖。肽段对SEA诱导功能的抑制至少部分是由于对携带Vβ3的T细胞活性的抑制,因为Vβ3 -(57 - 77)可显著降低与抗Vβ3单克隆抗体反应的T细胞百分比。这些数据表明,Vβ3中包含第57 - 77位氨基酸的区域是一个展示出与SEA分子结合并阻断由此产生的与T细胞抗原受体相互作用的合适序列和构象的区域。

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