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无细胞体系中嗜中性粒细胞呼吸爆发氧化酶的显微技术——氧化酶激活系统的特性

A microtechnique for neutrophil respiratory burst oxidase in a cell-free system--characterization of oxidase activation system.

作者信息

Umeki S, DeLisle D M

机构信息

Department of Medicine, Kawasaki Medical School, Okayama, Japan.

出版信息

Comp Biochem Physiol B. 1990;96(3):461-4. doi: 10.1016/0305-0491(90)90040-z.

Abstract
  1. A microtechnique for quantitating human neutrophil NADPH oxidase in a cell-free system is described. 2. This spectrophotometric discontinuous (fixed time) method is less material-consuming than existing methods and is more useful for experiments in which superoxide production by neutrophils must be measured in a large number of samples. 3. Measurement of NADPH oxidase using the new method can be accomplished in a final vol of 0.15 ml. 4. In the assay, neutrophil membranes solubilized with deoxycholate were incubated for 3 min with cytosolic fractions, magnesium, sodium dodecyl sulfate, and cytochrome c in the absence of NADPH to preincubate the oxidase before the addition of the reducing agent. 5. The reaction was started by adding NADPH and 2 min later terminated by adding superoxide dismutase. 6. The apparent Km for NADPH obtained by the new method was almost the same as that by the authorized method (39.2 +/- 3.1 SD vs 36.8 +/- 1.6). Activation of neutrophil NADPH oxidase was characterized using the new assay method.
摘要
  1. 描述了一种在无细胞体系中定量检测人中性粒细胞NADPH氧化酶的显微技术。2. 这种分光光度法间断(固定时间)方法比现有方法消耗材料更少,对于必须在大量样本中测量中性粒细胞产生超氧化物的实验更有用。3. 使用新方法测量NADPH氧化酶可在最终体积为0.15 ml的体系中完成。4. 在该测定中,用脱氧胆酸盐溶解的中性粒细胞膜在无NADPH的情况下与胞质部分、镁、十二烷基硫酸钠和细胞色素c孵育3分钟,以便在添加还原剂之前对氧化酶进行预孵育。5. 通过添加NADPH启动反应,并在2分钟后通过添加超氧化物歧化酶终止反应。6. 用新方法获得的NADPH的表观Km与权威方法几乎相同(39.2±3.1标准差对36.8±1.6)。使用新的测定方法对中性粒细胞NADPH氧化酶的激活进行了表征。

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