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核糖体肽基转移酶中心中具有中性pKa的单个腺苷。

A single adenosine with a neutral pKa in the ribosomal peptidyl transferase center.

作者信息

Muth G W, Ortoleva-Donnelly L, Strobel S A

机构信息

Department of Molecular Biophysics and Biochemistry, Yale University, 260 Whitney Avenue, New Haven, CT 06520-8114, USA.

出版信息

Science. 2000 Aug 11;289(5481):947-50. doi: 10.1126/science.289.5481.947.

Abstract

Biochemical and crystallographic evidence suggests that 23S ribosomal RNA (rRNA) is the catalyst of peptide bond formation. To explore the mechanism of this reaction, we screened for nucleotides in Escherichia coli 23S rRNA that may have a perturbed pKa (where Ka is the acid constant) based on the pH dependence of dimethylsulfate modification. A single universally conserved A (number 2451) within the central loop of domain V has a near neutral pKa of 7.6 +/- 0.2, which is about the same as that reported for the peptidyl transferase reaction. In vivo mutational analysis of this nucleotide indicates that it has an essential role in ribosomal function. These results are consistent with a mechanism wherein the nucleotide base of A2451 serves as a general acid base during peptide bond formation.

摘要

生化和晶体学证据表明,23S核糖体RNA(rRNA)是肽键形成的催化剂。为了探究该反应的机制,我们基于硫酸二甲酯修饰的pH依赖性,筛选了大肠杆菌23S rRNA中可能具有扰动pKa(其中Ka是酸常数)的核苷酸。结构域V中心环内的一个单一的普遍保守的A(编号2451)具有接近中性的pKa,为7.6±0.2,这与报道的肽基转移酶反应的pKa大致相同。对该核苷酸的体内突变分析表明,它在核糖体功能中起重要作用。这些结果与一种机制一致,即在肽键形成过程中,A2451的核苷酸碱基作为一般酸碱起作用。

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