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线粒体NADH:泛醌还原酶:牛75 kDa亚基导入前体的互补DNA序列。

Mitochondrial NADH:ubiquinone reductase: complementary DNA sequence of the import precursor of the bovine 75-kDa subunit.

作者信息

Runswick M J, Gennis R B, Fearnley I M, Walker J E

机构信息

Medical Research Council Laboratory of Molecular Biology, Cambridge, U.K.

出版信息

Biochemistry. 1989 Nov 28;28(24):9452-9. doi: 10.1021/bi00450a031.

DOI:10.1021/bi00450a031
PMID:2514801
Abstract

The 75-kDa subunit of complex I (NADH:ubiquinone oxidoreductase) from bovine heart mitochondria is its largest subunit and is a component of the iron-sulfur (IP) fragment of the enzyme. It is encoded in nuclear DNA and is imported into the organelle. Protein sequences have been determined at the N-terminus of the intact protein and on fragments generated by partial cleavage with cyanogen bromide and with Staphylococcus aureus protease V8. Parts of these data have been used to design two mixtures of oligonucleotides 17 bases long, containing 192 and 256 different sequences, which have been synthesized and used as hybridization probes for identification of cognate cDNA clones. Two different but overlapping clones have been isolated, and the sequences of the cloned DNAs have been determined. Together they code for a precursor of the 75-kDa subunit of complex I. The mature protein is 704 amino acids in length, has a calculated molecular mass of 75,961 daltons, and contains no segments of sequence that could be folded into hydrophobic alpha-helixes of sufficient length to span the inner membrane of the mitochondrion. Its precursor has an N-terminal extension of 23 amino acids to specify its import into the mitochondrion from the cytoplasm. Seventeen cysteine residues are dispersed throughout the 75-kDa subunit; some of them are close to each other in the sequence in three separate groups and, by analogy with other iron-sulfur proteins, could be involved in iron-sulfur clusters.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

牛心线粒体复合体I(NADH:泛醌氧化还原酶)的75 kDa亚基是其最大的亚基,是该酶铁硫(IP)片段的一个组成部分。它由核DNA编码,并被导入细胞器。已经确定了完整蛋白质N端以及用溴化氰和金黄色葡萄球菌蛋白酶V8部分切割产生的片段的蛋白质序列。这些数据的一部分已被用于设计两种由17个碱基组成的寡核苷酸混合物,分别包含192和256种不同序列,这些寡核苷酸已被合成并用作杂交探针来鉴定同源cDNA克隆。已分离出两个不同但重叠的克隆,并确定了克隆DNA的序列。它们共同编码复合体I的75 kDa亚基的前体。成熟蛋白长度为704个氨基酸,计算分子量为75,961道尔顿,并且不包含可折叠成足够长度以跨越线粒体内膜的疏水α螺旋的序列片段。其前体具有23个氨基酸的N端延伸,以指定其从细胞质导入线粒体。17个半胱氨酸残基分散在整个75 kDa亚基中;其中一些在序列中彼此靠近,分为三个独立的组,并且与其他铁硫蛋白类似,可能参与铁硫簇的形成。(摘要截断于250字)

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