Matern Julian C J, Bachmann Anne-Lena, Thiel Ilka V, Volkmann Gerrit, Wasmuth Alexandra, Binschik Jens, Mootz Henning D
Department of Chemistry and Pharmacy, Institute of Biochemistry, University of Muenster, Wilhelm-Klemm-Str. 2, 48149, Münster, Germany.
Methods Mol Biol. 2015;1266:129-43. doi: 10.1007/978-1-4939-2272-7_9.
Protein trans-splicing using split inteins is a powerful and convenient reaction to chemically modify recombinantly expressed proteins under mild conditions. In particular, semisynthetic protein trans-splicing with one intein fragment short enough to be accessible by solid-phase peptide synthesis can be used to transfer a short peptide segment with the desired synthetic moiety to the protein of interest. In this chapter, we provide detailed protocols for two such split intein systems. The M86 mutant of the Ssp DnaB intein and the MX1 mutant of the AceL-TerL intein are two highly engineered split inteins with very short N-terminal intein fragments of only 11 and 25 amino acids, respectively, and allow the efficient N-terminal labeling of proteins.
利用分裂内含肽进行蛋白质反式剪接是一种在温和条件下对重组表达的蛋白质进行化学修饰的强大且便捷的反应。特别地,半合成蛋白质反式剪接中使用的一个内含肽片段短到足以通过固相肽合成来获得,可用于将带有所需合成部分的短肽段转移到目标蛋白质上。在本章中,我们提供了两种此类分裂内含肽系统的详细方案。Ssp DnaB内含肽的M86突变体和AceL-TerL内含肽的MX1突变体是两种经过高度工程改造的分裂内含肽,其N端内含肽片段非常短,分别只有11和25个氨基酸,可实现蛋白质的高效N端标记。