Suppr超能文献

一种新的小鼠T细胞生长因子P40的完整氨基酸序列

Complete amino acid sequence of a new murine T-cell growth factor P40.

作者信息

Simpson R J, Moritz R L, Rubira M R, Gorman J J, Van Snick J

机构信息

Joint Protein Structure Laboratory, Ludwig Institute for Cancer Research (Melbourne Branch), Royal Melbourne Hospital, Parkville, Victoria, Australia.

出版信息

Eur J Biochem. 1989 Aug 15;183(3):715-22. doi: 10.1111/j.1432-1033.1989.tb21103.x.

Abstract

A new murine T-cell growth factor, designated P40, which supports growth of helper T-cells in the absence of interleukin-2, interleukin-4 and antigen has been isolated from helper T-cell lines in sufficient quantities (100 micrograms) to permit its complete amino acid sequence determination. This was achieved by a combination of sensitive peptide mapping using microbore reversed-phase high performance liquid chromatography and automated microsequence analysis. Attempts to obtain N-terminal sequence data on P40 were unsuccessful due to N-terminal blockage of the native molecule. The nature of this N-terminal blocking was established using a combination of amino acid analysis, fast-atom-bombardment mass spectrometry and peptide synthesis. The P40 molecule, a single polypeptide chain comprising 126 amino acid residues, is structurally distinct from other known T-cell growth factors. No similarity was revealed when the amino acid sequence of P40 was compared with other proteins whose biochemical structure is known. The protein sequence data reported here predict four N-linked glycosylation sites in the P40 molecule.

摘要

一种新的小鼠T细胞生长因子,命名为P40,已从辅助性T细胞系中大量分离出来(100微克),足以确定其完整的氨基酸序列。在没有白细胞介素-2、白细胞介素-4和抗原的情况下,它能支持辅助性T细胞的生长。这是通过使用微径反相高效液相色谱进行灵敏的肽图谱分析和自动微量序列分析相结合来实现的。由于天然分子的N端被封闭,试图获得P40的N端序列数据未成功。利用氨基酸分析、快原子轰击质谱和肽合成相结合的方法确定了这种N端封闭的性质。P40分子是一条由126个氨基酸残基组成的单多肽链,在结构上与其他已知的T细胞生长因子不同。将P40的氨基酸序列与其他已知生化结构的蛋白质进行比较时,未发现相似性。本文报道的蛋白质序列数据预测P40分子中有四个N-连接糖基化位点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验