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N-乙基马来酰亚胺反应性半胱氨酸在牛心线粒体ADP/ATP载体蛋白中的定位

Localization of the N-ethylmaleimide reactive cysteine in the beef heart mitochondrial ADP/ATP carrier protein.

作者信息

Boulay F, Vignais P V

出版信息

Biochemistry. 1984 Sep 25;23(20):4807-12. doi: 10.1021/bi00315a042.

Abstract

Alkylation of the ADP/ATP carrier protein in beef heart mitochondria by N-ethylmaleimide (NEM) results in inactivation of transport. One out of the four cysteinyl residues contained in 1 mol of carrier subunit of Mr 32 000 is alkylated by NEM. The identification of the alkylated residue to Cys-56 has been achieved by chemical and enzymatic cleavages. The chemical cleavages included cleavages at the nonalkylated cysteinyl residues by cyanide at alkaline pH and at methionyl residues by cyanogen bromide. Enzymatic cleavage involved the use of trypsin and chymotrypsin; the resulting peptides were resolved by high-performance liquid chromatography. Analysis of a small size [14C]NEM-labeled peptide obtained by tryptic and chymotryptic digestion of the [14C]NEM-labeled carrier protein yielded the following amino acid sequence: (Formula: see text) where X is probably a substituted lysine.

摘要

N-乙基马来酰亚胺(NEM)使牛心线粒体中的ADP/ATP载体蛋白发生烷基化,导致转运失活。Mr 32000的1摩尔载体亚基所含的四个半胱氨酰残基中有一个被NEM烷基化。通过化学和酶切已确定被烷基化的残基为Cys-56。化学切割包括在碱性pH下用氰化物切割未烷基化的半胱氨酰残基,以及用溴化氰切割甲硫氨酰残基。酶切使用了胰蛋白酶和糜蛋白酶;所得肽段通过高效液相色谱法分离。对经胰蛋白酶和糜蛋白酶消化[14C]NEM标记的载体蛋白得到的小尺寸[14C]NEM标记肽段进行分析,得到以下氨基酸序列:(公式:见文本)其中X可能是一个取代赖氨酸。

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