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小鼠ATP合酶α亚基的克隆与功能表达分析

Cloning and functional expression analysis of the alpha subunit of mouse ATP synthase.

作者信息

Yotov W V, St-Arnaud R

机构信息

Genetics Unit, Shriners Hospital for Crippled Children, Montréal, Québec, Canada.

出版信息

Biochem Biophys Res Commun. 1993 Feb 26;191(1):142-8. doi: 10.1006/bbrc.1993.1195.

Abstract

The alpha subunit of the mitochondrial ATP synthase is part of the F1 enzymatic complex known to bind ADP, phosphate and ATP and is at the heart of the mitochondrial energy-producing mechanism. The mouse embryonal carcinoma variant of the alpha subunit cDNA was cloned and the complete nucleotide sequences of two different lengths of clones were determined. Two distinct polyadenylation sites in the cDNA sequence were detected and two sizes of mRNAs were confirmed by Northern blot hybridization. Two putative ATP-binding motifs - A and B, have been hypothesized for this enzyme based on previous NMR work on another ATP-binding enzyme, adenylate kinase. We have constructed four deletion mutants of the alpha subunit of the mouse F1-ATP synthase to examine the putative role of these domains. The resulting recombinant proteins were expressed and purified. Functional studies with the immobilized mutants proved the significance of both sites for ATP binding.

摘要

线粒体ATP合酶的α亚基是F1酶复合物的一部分,已知该复合物可结合ADP、磷酸和ATP,并且是线粒体能量产生机制的核心。克隆了α亚基cDNA的小鼠胚胎癌细胞系变体,并测定了两个不同长度克隆的完整核苷酸序列。在cDNA序列中检测到两个不同的聚腺苷酸化位点,并通过Northern印迹杂交证实了两种大小的mRNA。基于先前对另一种ATP结合酶腺苷酸激酶的核磁共振研究,已为该酶推测了两个假定的ATP结合基序——A和B。我们构建了小鼠F1-ATP合酶α亚基的四个缺失突变体,以研究这些结构域的假定作用。表达并纯化了产生的重组蛋白。对固定化突变体的功能研究证明了这两个位点对ATP结合的重要性。

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