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人线粒体NADH-辅酶Q还原酶75-kDa铁硫蛋白cDNA序列的测定

Determination of the cDNA sequence for the human mitochondrial 75-kDa Fe-S protein of NADH-coenzyme Q reductase.

作者信息

Chow W, Ragan I, Robinson B H

机构信息

Department of Biochemistry and Paediatrics, University of Toronto, Canada.

出版信息

Eur J Biochem. 1991 Nov 1;201(3):547-50. doi: 10.1111/j.1432-1033.1991.tb16313.x.

Abstract

A human-hepatoma cDNA lambda gt11 expression library was probed with an antibody to holoenzyme complex I (NADH-CoQ reductase) of the respiratory chain. One of the 30 antibody positive clones was purified to homogeneity, amplified by the polymerase chain reaction (PCR), subcloned and sequenced. It proved to be highly similar to the cDNA sequence for the bovine 75-kDa Fe--S protein. Using the sequence obtained from this library, both sense and antisense oligonucleotides were constructed and used to probe a human kidney cDNA library using PCR amplification with oligonucleotides that flank the polylinker region of the lambda phage. Two further cDNA clones were obtained which overlapped and covered the entire cDNA sequence of 2526 bp. The encoded protein of 727 amino acids has 21 amino acids that differ from the bovine-protein sequence. Northern blot analysis of mRNA from fibroblasts of complex-I deficient patients revealed no abnormalities. We show that this Fe--S protein has significant similarity with (a) the gamma chain of the hydrogen hydrogenase of Alcaligenes eutrophus and (b) the A chain of the formate dehydrogenase of Methanobacterium formicum.

摘要

用人肝癌cDNAλgt11表达文库与呼吸链全酶复合物I(NADH - 辅酶Q还原酶)的抗体进行杂交。30个抗体阳性克隆中的一个被纯化至均一,通过聚合酶链反应(PCR)扩增,亚克隆并测序。结果证明它与牛75 kDa铁硫蛋白的cDNA序列高度相似。利用从该文库获得的序列,构建了正义和反义寡核苷酸,并使用与λ噬菌体多克隆位点区域侧翼的寡核苷酸进行PCR扩增,用于探测人肾cDNA文库。又获得了另外两个cDNA克隆,它们相互重叠并覆盖了2526 bp的完整cDNA序列。编码的727个氨基酸的蛋白质有21个氨基酸与牛蛋白质序列不同。对复合物I缺陷患者成纤维细胞的mRNA进行Northern印迹分析,未发现异常。我们发现这种铁硫蛋白与(a)嗜碱假单胞菌氢化酶的γ链和(b)甲酸甲烷杆菌甲酸脱氢酶的A链具有显著相似性。

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