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分枝杆菌的DNA结合蛋白与人体免疫反应

DNA binding protein of mycobacteria and human immune response.

作者信息

Prasad H K, Prabhakar S, Annapurna P S, Kaur S, Jain N K, Dey A B, Islam N, Raje M

机构信息

Department of Biotechnology, All India Institute of Medical Sciences, 110029 New Delhi.

出版信息

Indian J Clin Biochem. 1997 Dec;12(Suppl 1):86-8. doi: 10.1007/BF02873070.

Abstract

A dual step procedure was used to identify a 30 kDa DNA binding protein of mycobacteria (HLPMt) which is a target of human T and B cell response. The immunodominance of HLPMt was estabished by T cell blot assay as well as by subtractive immunoblot assay. This protein is not secreted into the extracellular culture fluid and is different from the 85 ABC complex of proteins as seen by immunoblots and ELISA. The protein is capable of inducingin vitro lymphoproliferation in tuberculin reactors. The protein was purified for the generation of monospecific sera and for amino acid sequencing. The sequence of the 16 amino acid long peptide derived from the 30 kDa protein showed a 100% homology with the translated sequence of a cosmid cY349 (Sanger Centre, Cambridge, UK). The ORF was predicted to code for a protein of 214 amino acids. Oligonucleotide primers were designed against the 5' and 3' end of the gene and the gene was PCR amplified, cloned and expressed inE.coli. The protein has unique dual domains which show homology to both bacterial HU proteins and to eukaryotic histones H1.

摘要

采用双步程序鉴定了分枝杆菌的一种30 kDa DNA结合蛋白(HLPMt),它是人类T细胞和B细胞反应的靶标。通过T细胞印迹分析以及消减免疫印迹分析确定了HLPMt的免疫显性。该蛋白不分泌到细胞外培养液中,并且通过免疫印迹和酶联免疫吸附测定法可知其与85 ABC蛋白复合物不同。该蛋白能够在结核菌素反应者中诱导体外淋巴细胞增殖。为了产生单特异性血清和进行氨基酸测序,对该蛋白进行了纯化。从30 kDa蛋白衍生的16个氨基酸长的肽段序列与黏粒cY349(英国剑桥桑格中心)的翻译序列显示出100%的同源性。预测该开放阅读框编码一种214个氨基酸的蛋白质。针对该基因的5'端和3'端设计了寡核苷酸引物,并通过聚合酶链反应扩增、克隆该基因并在大肠杆菌中表达。该蛋白具有独特的双结构域,与细菌HU蛋白和真核组蛋白H1均显示出同源性。

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