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探索密码子和反密码子大小的极限。

Exploring the limits of codon and anticodon size.

作者信息

Anderson J Christopher, Magliery Thomas J, Schultz Peter G

机构信息

Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.

出版信息

Chem Biol. 2002 Feb;9(2):237-44. doi: 10.1016/s1074-5521(02)00094-7.

Abstract

We previously employed a combinatorial approach to identify the most efficient suppressors of four-base codons in E. coli. We have now examined the suppression of two-, three-, four-, five-, and six-base codons with tRNAs containing 6-10 nt in their anticodon loops. We found that the E. coli translational machinery tolerates codons of 3-5 bases and that tRNAs with 6-10 nt anticodon loops can suppress these codons. However, N-length codons were found to prefer N + 4-length anticodon loops. Additionally, sequence preferences, including the requirement of Watson-Crick complementarity to the codon, were evident in the loops. These selections have yielded efficient suppressors of four-base and five-base codons for our ongoing efforts to expand the genetic code. They also highlight some of the parameters that underlie the fidelity of frame maintenance.

摘要

我们之前采用了一种组合方法来鉴定大肠杆菌中四碱基密码子的最有效抑制子。现在我们研究了反密码子环中含有6-10个核苷酸的tRNA对二碱基、三碱基、四碱基、五碱基和六碱基密码子的抑制作用。我们发现大肠杆菌的翻译机制能够容忍3-5个碱基的密码子,并且反密码子环含有6-10个核苷酸的tRNA能够抑制这些密码子。然而,发现N长度的密码子更喜欢N + 4长度的反密码子环。此外,环中存在序列偏好,包括与密码子的沃森-克里克互补性要求。这些筛选为我们正在进行的扩展遗传密码的工作产生了四碱基和五碱基密码子的有效抑制子。它们还突出了一些构成维持读框保真度基础的参数。

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