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T淋巴细胞和B淋巴细胞上表达的大膜蛋白(LMP)之间的分子关系。

Molecular relationships between large membrane proteins (LMP) expressed on T and B lymphocytes.

作者信息

Dunlap B, Mixter P F, Koller B, Watson A, Widmer M B, Bach F H

出版信息

J Immunol. 1980 Oct;125(4):1829-31.

PMID:6447731
Abstract

Clones prepared from day 5 mixed lymphocyte cultures (MLC) were examined for the expression of large (170,000- to 200,000-dalton) membrane proteins (LMP), found on bulk cultures of resting and allogeneically activated T lymphocytes. Sodium dodecyl sulfate-poly-acrylamide gel electrophoresis (SDS-PAGE) of these proteins indicates both bulk populations and noncytotoxic clones express LMP of similar m.w. Peptide mapping further indicates that LMP of 187,000 (187K) and 200K daltons, found on T cells from bulk cultures or clones and the 220K dalton LMP from B cells, all appear to have a very similar peptide composition. This suggests a single protein (or series of closely related proteins) is differentially processed in functionally disparate populations, and hence may serve as a differentiation antigen for these populations.

摘要

对从第5天混合淋巴细胞培养物(MLC)制备的克隆进行检测,以确定大分子量(170,000至200,000道尔顿)膜蛋白(LMP)的表达情况,该蛋白存在于静止和同种异体激活的T淋巴细胞的大量培养物中。这些蛋白的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)表明,大量细胞群体和无细胞毒性的克隆均表达分子量相似的LMP。肽图谱分析进一步表明,在大量培养物或克隆的T细胞上发现的187,000(187K)和200K道尔顿的LMP,以及来自B细胞的220K道尔顿的LMP,似乎都具有非常相似的肽组成。这表明单一蛋白质(或一系列密切相关的蛋白质)在功能不同的细胞群体中进行了差异加工,因此可能作为这些细胞群体的分化抗原。

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