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T细胞对因单个氨基酸替换而选择性改变的Ia分子的识别。

T-cell recognition of Ia molecules selectively altered by a single amino acid substitution.

作者信息

Brown M A, Glimcher L A, Nielsen E A, Paul W E, Germain R N

出版信息

Science. 1986 Jan 17;231(4735):255-8. doi: 10.1126/science.3484558.

Abstract

T lymphocytes recognize foreign antigen together with allele-specific determinants on membrane-bound class I and class II (Ia) gene products of the major histocompatibility complex. To identify amino acids of class II molecules critical to this recognition process, the genes encoding the beta chains of the I-Ak molecule were cloned from a wild-type B-cell hybridoma and from an immunoselected variant subline showing distinct serological and T-cell stimulatory properties. Nucleotide sequencing and DNA-mediated gene transfer established that a single base transition (G----A) encoding a change from glutamic acid to lysine at position 67 in the I-Ak beta molecule accounted for all the observed phenotypic changes of the variant cells. These results confirm the importance of residues 62 to 78 in the amino terminal domain of I-A beta for class II-restricted T-cell recognition of antigen and demonstrate the ability of a single substitution in this region to alter this recognition event.

摘要

T淋巴细胞与主要组织相容性复合体的膜结合I类和II类(Ia)基因产物上的等位基因特异性决定簇一起识别外来抗原。为了确定II类分子中对这一识别过程至关重要的氨基酸,从野生型B细胞杂交瘤和显示出不同血清学和T细胞刺激特性的免疫选择变异亚系中克隆了编码I-Ak分子β链的基因。核苷酸测序和DNA介导的基因转移证实,I-Akβ分子第67位的一个碱基转换(G→A)导致谷氨酸变为赖氨酸,这解释了变异细胞所有观察到的表型变化。这些结果证实了I-Aβ氨基末端结构域中62至78位残基对于II类限制性T细胞对抗原的识别的重要性,并证明了该区域的单个取代能够改变这一识别事件。

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