Suppr超能文献

大肠杆菌甲硫氨酰-tRNA合成酶的tRNA识别位点。

tRNA recognition site of Escherichia coli methionyl-tRNA synthetase.

作者信息

Leon O, Schulman L H

机构信息

Department of Developmental Biology and Cancer, Albert Einstein College of Medicine, Bronx, New York 10461.

出版信息

Biochemistry. 1987 Aug 25;26(17):5416-22. doi: 10.1021/bi00391a030.

Abstract

We have previously shown that anticodon bases are essential for specific recognition of tRNA substrates by Escherichia coli methionyl-tRNA synthetase (MetRS) [Schulman, L. H., & Pelka, H. (1983) Proc. Natl. Acad. Sci. U.S.A. 80, 6755-6759] and that the enzyme tightly binds to C34 at the wobble position of E. coli initiator methionine tRNA (tRNAfMet) [Pelka, H., & Schulman, L. H. (1986) Biochemistry 25, 4450-4456]. We have also previously demonstrated that an affinity labeling derivative of tRNAfMet can be quantitatively cross-linked to the tRNA binding site of MetRS [Valenzuela, D., & Schulman, L. H. (1986) Biochemistry 25, 4555-4561]. Here, we have determined the site in MetRS which is cross-linked to the anticodon of tRNAfMet, as well as the location of four additional cross-links. Only a single peptide, containing Lys465, is covalently coupled to C34, indicating that the recognition site for the anticodon is close to this sequence in the three-dimensional structure of MetRS. The D loop at one corner of the tRNA molecule is cross-linked to three peptides, containing Lys402, Lys439, and Lys596. The 5' terminus of the tRNA is cross-linked to Lys640, near the carboxy terminus of the enzyme. Since the 3' end of tRNAfMet is positioned close to the active site in the N-terminal domain [Hountondji, C., Blanquet, S., & Lederer, F. (1985) Biochemistry 24, 1175-1180], this result indicates that the carboxy ends of the two polypeptide chains of native dimeric MetRS are folded back toward the N-terminal domain of each subunit.

摘要

我们之前已经表明,反密码子碱基对于大肠杆菌甲硫氨酰 - tRNA合成酶(MetRS)特异性识别tRNA底物至关重要[舒尔曼,L. H.,& 佩尔卡,H.(1983年)《美国国家科学院院刊》80,6755 - 6759],并且该酶与大肠杆菌起始甲硫氨酸tRNA(tRNAfMet)摆动位置的C34紧密结合[佩尔卡,H.,& 舒尔曼,L. H.(1986年)《生物化学》25,4450 - 4456]。我们之前还证明,tRNAfMet的一种亲和标记衍生物可以定量交联到MetRS的tRNA结合位点[巴伦苏埃拉,D.,& 舒尔曼,L. H.(1986年)《生物化学》25,4555 - 4561]。在此,我们确定了MetRS中与tRNAfMet反密码子交联的位点,以及另外四个交联的位置。只有一个包含赖氨酸465的肽共价偶联到C34,这表明反密码子的识别位点在MetRS三维结构中靠近该序列。tRNA分子一个角上的D环交联到三个肽,分别包含赖氨酸402、赖氨酸439和赖氨酸596。tRNA的5'末端交联到靠近酶羧基末端的赖氨酸640。由于tRNAfMet的3'末端位于N末端结构域的活性位点附近[洪通吉,C.,布兰凯,S.,& 勒德雷尔,F.(1985年)《生物化学》24,1175 - 1180],这一结果表明天然二聚体MetRS的两条多肽链的羧基末端向每个亚基的N末端结构域折叠回去。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验