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N-甲酰化蛋白在大肠杆菌中的表达。

Expression of N-formylated proteins in Escherichia coli.

作者信息

Spector Shari, Flynn Julia M, Tidor Bruce, Baker Tania A, Sauer Robert T

机构信息

Department of Biology, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.

出版信息

Protein Expr Purif. 2003 Dec;32(2):317-22. doi: 10.1016/j.pep.2003.08.004.

Abstract

In bacteria, protein expression initiates with a formyl-methionine group. Addition of the antibiotic actinonin, a known peptide deformylase inhibitor, at the time of induction of protein expression results in the retention of the formyl group by the overexpressed protein. In addition, because deformylation is a prerequisite for removal of the initiating methionine, this post-translational processing step is also prevented by actinonin, and the N-formyl methionine residue is retained by proteins from which it is normally removed. We have demonstrated the applicability of this system for obtaining N-modified forms of several different proteins and use one of these modified molecules to show that the N-terminal amino group is not required for ClpXP degradation of proteins bearing an N-terminal recognition signal.

摘要

在细菌中,蛋白质表达起始于一个甲酰甲硫氨酸基团。在蛋白质表达诱导时添加抗生素放线菌素(一种已知的肽脱甲酰基酶抑制剂),会导致过表达的蛋白质保留甲酰基。此外,由于脱甲酰化是去除起始甲硫氨酸的前提条件,这一翻译后加工步骤也会被放线菌素阻止,并且N-甲酰甲硫氨酸残基会被通常会将其去除的蛋白质保留。我们已经证明了该系统在获得几种不同蛋白质的N-修饰形式方面的适用性,并使用其中一种修饰分子表明,对于带有N端识别信号的蛋白质的ClpXP降解而言,N端氨基并非必需。

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