Kindermann Maik, George Nathalie, Johnsson Nils, Johnsson Kai
Institute of Molecular and Biological Chemistry, Swiss Federal Institute of Technology, CH-1015 Lausanne, Switzerland.
J Am Chem Soc. 2003 Jul 2;125(26):7810-1. doi: 10.1021/ja034145s.
A general method for the covalent immobilization of fusion proteins is presented. The approach is based on the unusual mechanism of the human O6-alkylguanine-DNA alkyltransferase, which irreversibly transfers the alkyl group from its substrate, alkylated or benzylated guanine, to a reactive cysteine residue. By attaching the benzyl group to a surface, hAGT fusion proteins immobilize themselves in a specific and covalent manner. The specificity of the reaction of hAGT with its substrate even allows the specific immobilization of hAGT fusion proteins directly out of cell extracts, making the approach an attractive alternative to currently used immobilization procedures.
本文介绍了一种融合蛋白共价固定的通用方法。该方法基于人O6-烷基鸟嘌呤-DNA烷基转移酶的独特机制,该酶可将其底物(烷基化或苄基化鸟嘌呤)上的烷基不可逆地转移至一个反应性半胱氨酸残基上。通过将苄基连接到表面,hAGT融合蛋白以特定的共价方式固定自身。hAGT与其底物反应的特异性甚至使得hAGT融合蛋白能够直接从细胞提取物中特异性固定,这使得该方法成为当前使用的固定程序的一个有吸引力的替代方法。