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波卓霉素A2的作用模式:波卓霉素A2对多核糖体的影响。

Mode of action of bottromycin A2: effect of bottromycin A2 on polysomes.

作者信息

Otaka T, Kaji A

出版信息

FEBS Lett. 1983 Mar 7;153(1):53-9. doi: 10.1016/0014-5793(83)80118-5.

Abstract

When bottromycin A2 was added to an in vitro protein synthesis system carried out by naturally occurring polysomes, it inhibited protein synthesis effectively. Examination of the 3 steps of peptide chain elongation revealed that the binding of aminoacyl-tRNA to the polyribosomes was inhibited by bottromycin A2. In contrast, we concluded that the peptide bond formation and the translocation steps in this system were not inhibited by bottromycin A2 on the basis of the following observations: (1) The break-down of polysomes, which is dependent on EFG, puromycin and RR (ribosome releasing) factor, was insensitive to bottromycin A2; (2) The puromycin dependent release of polypeptide from polysomes, with or without EFG, was not inhibited by bottromycin A2. Thus bottromycin specifically interferes with proper functioning of the A sites of polysomes. This is consistent with the results obtained using the model system with synthetic polynucleotides.

摘要

当将波卓霉素A2添加到由天然存在的多核糖体进行的体外蛋白质合成系统中时,它能有效抑制蛋白质合成。对肽链延伸的三个步骤进行检查发现,氨酰tRNA与多核糖体的结合受到波卓霉素A2的抑制。相比之下,基于以下观察结果,我们得出结论:该系统中的肽键形成和转位步骤不受波卓霉素A2的抑制:(1)依赖于延伸因子G、嘌呤霉素和核糖体释放因子的多核糖体解体对波卓霉素A2不敏感;(2)无论有无延伸因子G,嘌呤霉素依赖的多核糖体上多肽的释放均不受波卓霉素A2的抑制。因此,波卓霉素特异性干扰多核糖体A位点的正常功能。这与使用合成多核苷酸的模型系统获得的结果一致。

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