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与T细胞识别决定簇相关的HLA DRβ1等位基因的序列多态性。

Sequence polymorphism of HLA DR beta 1 alleles relating to T-cell-recognized determinants.

作者信息

Cairns J S, Curtsinger J M, Dahl C A, Freeman S, Alter B J, Bach F H

出版信息

Nature. 1985;317(6033):166-8. doi: 10.1038/317166a0.

Abstract

HLA class II molecules are a highly polymorphic family of dimeric cell-surface proteins primarily involved in regulating T-cell responses to extrinsic antigens. To define regions of class II molecules involved in T-cell recognition, we have now compared sequences of three HLA DR beta cDNA clones obtained from cells that all express the same serologically defined determinants but differ in terms of T-cell-recognized specificities. The comparisons indicate that very few (one to four) nucleotides differ between what are almost certainly alleles of the DR beta 1 locus. All differences were in the first domain of the molecule and all localized to a region from amino acids 71-86. Because all differences were found only in this region of the molecule, and because DR alpha-chains seem to be relatively non-polymorphic, these positions in the DR beta-chain must have a major role in influencing T-cell recognition of the DR molecule.

摘要

HLA II类分子是一类高度多态性的二聚体细胞表面蛋白家族,主要参与调节T细胞对外源性抗原的反应。为了确定II类分子中参与T细胞识别的区域,我们现在比较了从细胞中获得的三个HLA DRβ cDNA克隆的序列,这些细胞都表达相同的血清学定义的决定簇,但在T细胞识别特异性方面有所不同。比较结果表明,几乎可以肯定是DRβ1基因座等位基因的序列之间只有很少(一到四个)核苷酸不同。所有差异都在分子的第一个结构域,并且都定位在氨基酸71 - 86的区域。由于所有差异仅在分子的该区域中发现,并且由于DRα链似乎相对非多态性,因此DRβ链中的这些位置在影响T细胞对DR分子的识别中必定起主要作用。

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