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DNA binding protein of mycobacteria and human immune response

机译:分枝杆菌的DNA结合蛋白与人体免疫反应

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摘要

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.
机译:使用双步骤程序鉴定了分枝杆菌的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细胞印迹测定以及减免免疫印迹测定可确定HLPMt的免疫优势。这种蛋白质不会分泌到细胞外培养液中,并且与免疫印迹和ELISA所见的蛋白质的85 ABC复合物不同。该蛋白能够在结核菌素反应器中诱导体外淋巴细胞增殖。纯化蛋白质以产生单特异性血清并用于氨基酸测序。衍生自30 kDa蛋白的16个氨基酸长的肽序列与粘粒cY349(Sanger Centre,Cambridge,UK)的翻译序列具有100%的同源性。预测ORF编码214个氨基酸的蛋白质。针对该基因的5'和3'末端设计寡核苷酸引物,并对该基因进行PCR扩增,克隆并在大肠杆菌中表达。该蛋白具有独特的双重结构域,与细菌HU蛋白和真核组蛋白H1都具有同源性。

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