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一种可有可无的酵母核糖体蛋白可优化肽基转移酶活性并影响转位。

A dispensable yeast ribosomal protein optimizes peptidyltransferase activity and affects translocation.

作者信息

Dresios John, Panopoulos Panagiotis, Suzuki Katsuyuki, Synetos Dennis

机构信息

Laboratory of Biochemistry, School of Medicine, University of Patras, 26110 Patras, Greece.

出版信息

J Biol Chem. 2003 Jan 31;278(5):3314-22. doi: 10.1074/jbc.M207533200. Epub 2002 Nov 13.

Abstract

Yeast ribosomal protein L41 is dispensable in the yeast. Its absence had no effect on polyphenylalanine synthesis activity, and a limited effect on growth, translational accuracy, or the resistance toward the antibiotic paromomycin. Removal of L41 did not affect the 60:40 S ratio, but it reduced the amount of 80 S, suggesting that L41 is involved in ribosomal subunit association. However, the two most important effects of L41 were on peptidyltransferase activity and translocation. Peptidyltransferase activity was measured as a second-order rate constant (k(cat)/K(s)) corresponding to the rate of peptide bond formation; this k(cat)/K(s) was lowered 3-fold to 1.15 min(-1) mm(-1) in the L41 mutant compared with 3.46 min(-1) mm(-1) in the wild type. Translocation was also affected by L41. Elongation factor 2 (EF2)-dependent (enzymatic) translocation of Ac-Phe-tRNA from the A- to P-site was more efficient in the absence of L41, because 50% translocation was achieved at only 0.004 microm EF2 compared with 0.02 microm for the wild type. Furthermore, the EF2-dependent translocation was inhibited by 50% at 2.5 microm of the translocation inhibitor cycloheximide in the L41 mutant compared with 1.2 microm in the wild type. Finally, the rate of EF2-independent (spontaneous) translocation was increased in the absence of L41.

摘要

酵母核糖体蛋白L41在酵母中是可有可无的。它的缺失对多聚苯丙氨酸合成活性没有影响,对生长、翻译准确性或对抗生素巴龙霉素的抗性影响有限。去除L41并不影响60:40 S的比例,但会减少80 S的数量,这表明L41参与核糖体亚基的结合。然而,L41的两个最重要的作用是对肽基转移酶活性和转位。肽基转移酶活性以对应于肽键形成速率的二级速率常数(k(cat)/K(s))来衡量;与野生型的3.46 min(-1) mm(-1)相比,L41突变体中的这个k(cat)/K(s)降低了3倍,至1.15 min(-1) mm(-1)。转位也受到L41的影响。在没有L41的情况下,Ac-Phe-tRNA从A位点到P位点的延伸因子2(EF2)依赖性(酶促)转位更有效,因为在仅0.004微摩尔EF2时就实现了50%的转位,而野生型为0.02微摩尔。此外,在L41突变体中,2.5微摩尔的转位抑制剂环己酰亚胺对EF2依赖性转位的抑制率为50%,而野生型为1.2微摩尔。最后,在没有L41的情况下,EF2非依赖性(自发)转位的速率增加。

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