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吞噬细胞NADPH氧化酶的黄素细胞色素b558亚基的化学计量学

Stoichiometry of the subunits of flavocytochrome b558 of the NADPH oxidase of phagocytes.

作者信息

Wallach T M, Segal A W

机构信息

Department of Medicine, University College London, Bayne Institute, U.K.

出版信息

Biochem J. 1996 Nov 15;320 ( Pt 1)(Pt 1):33-8. doi: 10.1042/bj3200033.

Abstract

Flavocytochrome b558, the membrane-spanning component of the NADPH oxidase system of phagocytic cells, is composed of two subunits, p22phox and gp91phox (where phox stands for phagocyte oxidase). The stoichiometry of the subunits has been determined for purified flavocytochrome b556 by: (1) densitometry of Coomassie Blue-stained proteins separated by SDS/PAGE, (2) aromatic absorbance at 280 mm by the subunits after separation by gel filtration under denaturing conditions, (3) crosslinking studies with bis[sulphosuccinimidyl]suberate, where the molecular mass of the cross-linked complex was determined by Western blotting, and (4) radiolabelling of pure flavocytochrome b556 on lysine residues with 125I-labelled Bolton-Hunter reagent (N-succinimidyl-3-(4-hydroxy-5-[125I]iodophenyl)propionate), followed by SDS/PAGE and determination of the radioactivity on each subunit. The ratio of p22phox to gp91phox in the purified flavocytochrome b556 was related back to that in the neutrophil membrane by quantitative Western and dot-blotting to ensure that the stoichiometry was maintained during purification. These measurements showed that the two subunits were present in neutrophil membranes in a molar ratio of 1:1.

摘要

黄素细胞色素b558是吞噬细胞NADPH氧化酶系统的跨膜成分,由两个亚基组成,即p22phox和gp91phox(其中phox代表吞噬细胞氧化酶)。已通过以下方法确定了纯化的黄素细胞色素b556中亚基的化学计量比:(1)对SDS/PAGE分离的考马斯亮蓝染色蛋白进行光密度测定;(2)在变性条件下通过凝胶过滤分离后,测定亚基在280nm处的芳香族吸光度;(3)用双[磺基琥珀酰亚胺基]辛二酸酯进行交联研究,通过蛋白质印迹法确定交联复合物的分子量;(4)用125I标记的博尔顿-亨特试剂(N-琥珀酰亚胺基-3-(4-羟基-5-[125I]碘苯基)丙酸酯)对纯黄素细胞色素b556的赖氨酸残基进行放射性标记,随后进行SDS/PAGE并测定每个亚基上的放射性。通过定量蛋白质印迹和斑点印迹法,将纯化的黄素细胞色素b556中p22phox与gp91phox的比例追溯到中性粒细胞膜中的比例,以确保在纯化过程中化学计量比保持不变。这些测量结果表明,中性粒细胞膜中这两个亚基的摩尔比为1:1。

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