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大鼠红细胞超氧化物歧化酶的免疫定量分析:其在铜缺乏症中的应用。

Immunoquantitation of rat erythrocyte superoxide dismutase: its use in copper deficiency.

作者信息

Levieux A, Levieux D, Lab C

机构信息

Unité Immunochimie, SRV, INRA, St. Genès-Champanelle, France.

出版信息

Free Radic Biol Med. 1991;11(6):589-95. doi: 10.1016/0891-5849(91)90140-x.

Abstract

Two immunoassays have been developed for the determination of rat erythrocyte dismutase (Cu,Zn-SOD). An enzyme-linked immunosorbent assay (ELISA) was very sensitive down to 4 ng/ml with a coefficient of variation (CV) of 18% while the single radial immunodiffusion assay (SRID) permitted an adequate detection level (5 micrograms/ml) with far better accuracy (CV = 4.2%). The latter was thus selected for the determination of Cu,Zn-SOD in the red blood cells of normal and copper-depleted rats. The average value of Cu,Zn-SOD in normal adult rat erythrocytes was 1142 +/- 120 ng/mg hemoglobin. When compared to activity measurements, good correlation was obtained between enzyme content and enzyme activity (r = 0.803, P less than .001). In an experimental copper deficiency followed by supplementation, good correlation was observed in the course of depletion (r = 0.848, P less than .001) and repletion (r = 0.896, P less than .001). During depletion, the loss of enzyme activity was mainly related to a loss of enzyme. However, enzymatically inactive protein was formed which would be activated when copper was added. These results indicate the importance of a combined use of Cu,Zn-SOD immunoquantitation and activity measurements to enable a better understanding of changes occurring with respect to enzyme activity.

摘要

已开发出两种免疫测定法用于测定大鼠红细胞超氧化物歧化酶(铜锌超氧化物歧化酶)。一种酶联免疫吸附测定法(ELISA)非常灵敏,检测下限可达4纳克/毫升,变异系数(CV)为18%,而单向辐射免疫扩散测定法(SRID)的检测水平适中(5微克/毫升),准确性更高(CV = 4.2%)。因此,选用后者来测定正常大鼠和缺铜大鼠红细胞中的铜锌超氧化物歧化酶。正常成年大鼠红细胞中铜锌超氧化物歧化酶的平均值为1142±120纳克/毫克血红蛋白。与活性测量值相比,酶含量与酶活性之间具有良好的相关性(r = 0.803,P <.001)。在实验性缺铜并随后补充铜的过程中,在缺铜阶段(r = 0.848,P <.001)和补充阶段(r = 0.896,P <.001)均观察到良好的相关性。在缺铜期间,酶活性的丧失主要与酶的丢失有关。然而,会形成无酶活性的蛋白质,在添加铜后这些蛋白质会被激活。这些结果表明,联合使用铜锌超氧化物歧化酶免疫定量法和活性测量法对于更好地理解酶活性变化具有重要意义。

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