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用于测定金属酶中皮克级金属含量的微分析系统,以含锌酶为例。

Microanalytical system for determination of picogram quantities of metals in metalloenzymes, as illustrated with zinc-containing enzymes.

作者信息

Kawaguchi H, Auld D S

出版信息

Clin Chem. 1975 Apr;21(4):591-4.

PMID:46797
Abstract

Microwave-induced emission spectrometry combined with gel-exclusion chromatography provides a microanalytical system capable of precisely measuring 10 minus 10 to 10 minus 13 g of metal in microgram amounts of enzyme. Such sensitivity greatly exceeds that of other, more conventional methods. Metal quenching agents and low-molecular-weight protein contaminants were removed from the enzyme by Sephadex G-100 chromatography in microbore columns (0.03 times 25 cm). Droplet fractions were analyzed for zinc by the present method, for enzyme activity, and for protein content. With this analytical system we could demonstrate that stoichiometric amounts of zinc are present in the RNA-dependent DNA polymerase, the reverse transcriptase, from wooly monkey type C RNA tumor virus. The precision of the method for zinc was demonstrated by the coefficient of variation of 4.4 percent for 10 mug of zinc per liter. Validity and accuracy of the method were established by determining zinc in a series of zinc metalloenzymes of known metal content and stoichiometry.

摘要

微波诱导发射光谱法与凝胶排阻色谱法相结合,提供了一种微量分析系统,能够精确测量微克量酶中10的负10次方至10的负13次方克的金属。这种灵敏度大大超过了其他更传统方法的灵敏度。通过在微径柱(0.03×25厘米)中进行Sephadex G - 100色谱法,从酶中去除金属淬灭剂和低分子量蛋白质污染物。通过本方法分析液滴级分中的锌、酶活性和蛋白质含量。使用该分析系统,我们能够证明来自绒毛猴C型RNA肿瘤病毒的RNA依赖性DNA聚合酶(逆转录酶)中存在化学计量的锌。该方法对锌的精密度通过每升10微克锌的变异系数为4.4%得到证明。通过测定一系列已知金属含量和化学计量的锌金属酶中的锌,确定了该方法的有效性和准确性。

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