Miki T, Yoshida L S, Kakinuma K
Department of Inflammation Research, Tokyo Metropolitan Institute of Medical Science, Japan.
J Biol Chem. 1992 Sep 15;267(26):18695-701.
Cytochrome b558 of pig blood neutrophils was purified from the membranes of resting cells to examine its ability to reconstitute superoxide (O2-)-forming NADPH oxidase activity in a cell-free assay system containing cytosol and fatty acid. The membrane-associated cytochrome b558 was solubilized with a detergent, n-heptyl beta-thioglucoside, and purified by DEAE-Sepharose, heparin-Sepharose, and Mono Q column chromatography. The final preparation of cytochrome containing 11.5 nmol of protoheme/mg of protein gave bands of the large and small subunits on immunoblotted gel. The cell-free system with the purified cytochrome alone as a membrane component showed little O2(-)-generating activity in the absence of exogenous FAD. However, the system showed high O2(-)-generating activity of 31.8 mol/s/mol of cytochrome b558 (52.5% of the original O2(-)-generating activity of the solubilized membranes) in the presence of a nitro blue tetrazolium (NBT) reductase fraction that was separated from the cytochrome b fraction by heparin-Sepharose chromatography. Heat treatment of the NBT reductase fraction resulted in loss of the O2(-)-generating activity in the reconstituted system. The O2(-)-forming activity of the reconstituted system was markedly decreased by removal of FAD from the NBT reductase fraction and was restored by readdition of FAD to the FAD-depleted reductase. The reconstituted system containing purified cytochrome b558 plus the NBT reductase showed approximately 100 times higher O2(-)-generating activity than a system containing rabbit liver NADPH-cytochrome P-450 reductase instead. These results suggest that both the FAD-dependent NBT reductase and cytochrome b558 are required as membrane redox components for O2(-)-forming NADPH oxidase activity. The present data are discussed in comparison with previously reported results on reconstituted systems containing added free FAD.
从静息细胞的膜中纯化猪血中性粒细胞的细胞色素b558,以检测其在含有胞质溶胶和脂肪酸的无细胞检测系统中重建超氧化物(O2-)生成型NADPH氧化酶活性的能力。膜相关细胞色素b558用去污剂正庚基β-硫代葡萄糖苷溶解,并通过DEAE-琼脂糖、肝素-琼脂糖和Mono Q柱色谱法纯化。最终制备的含有11.5 nmol原卟啉/mg蛋白质的细胞色素在免疫印迹凝胶上呈现大小亚基条带。仅以纯化的细胞色素作为膜成分的无细胞系统在没有外源FAD的情况下几乎没有O2(-)生成活性。然而,在存在通过肝素-琼脂糖色谱法与细胞色素b部分分离的硝基蓝四唑(NBT)还原酶部分的情况下,该系统显示出31.8 mol/s/mol细胞色素b558的高O2(-)生成活性(溶解膜的原始O2(-)生成活性的52.5%)。对NBT还原酶部分进行热处理导致重建系统中O2(-)生成活性丧失。从NBT还原酶部分去除FAD会显著降低重建系统的O2(-)形成活性,通过向FAD耗尽的还原酶中重新添加FAD可恢复该活性。与包含纯化细胞色素b558和NBT还原酶的重建系统相比,包含兔肝NADPH-细胞色素P-450还原酶的系统的O2(-)生成活性大约高100倍。这些结果表明,FAD依赖性NBT还原酶和细胞色素b558都是O2(-)形成型NADPH氧化酶活性所需的膜氧化还原成分。将目前的数据与先前报道的关于添加游离FAD的重建系统的结果进行了比较讨论。