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一种用于测量脑蛋白合成的简单可重复的无细胞系统。

A simple reproducible cell-free system for measuring brain protein synthesis.

作者信息

Fando J L, Wasterlain C G

出版信息

Neurochem Res. 1980 Feb;5(2):197-207. doi: 10.1007/BF00964332.

Abstract

A simple, rapid, sensitive, and reproducible cell-free assay system for studying brain protein synthesis is described. This system uses small amounts of brain postmitochondrial supernatant, making it a convenient screening test when only small amounts of tissue are available. It showed over 95% dependence on Mg2+ and on an energy source. Optimal incorporation occurred under the following conditions: Mg2+ 3 mM; ATP, 0.6 mM; GTP, 0.6 mM; high K+, greater than or equal to 25 mM; Low Na+, less than or equal to 15 mM; pH 7.1-7.5. The rate of amino acid incorporation did not vary with leucine concentrations in vitro up to 1 mM, which obviated the need to measure endogenous leucine concentrations.

摘要

本文描述了一种用于研究脑蛋白合成的简单、快速、灵敏且可重复的无细胞检测系统。该系统使用少量脑线粒体后上清液,当仅有少量组织可用时,它成为一种便捷的筛选测试方法。它显示出对Mg2+和能量来源的依赖性超过95%。在以下条件下发生最佳掺入:Mg2+ 3 mM;ATP,0.6 mM;GTP,0.6 mM;高K+,大于或等于25 mM;低Na+,小于或等于15 mM;pH 7.1 - 7.5。在体外,直至1 mM的亮氨酸浓度下,氨基酸掺入速率并不随亮氨酸浓度变化,这使得无需测量内源性亮氨酸浓度。

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