一个由-甲乙醇诱导的启用结合,用于化学蛋白质合成

Cuicui Li1, Wenge Ma1, Kang Jin1

  • 1Department of Medicinal Chemistry, Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmacy, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.

概括

一种新的化学结合法使得从未受保护的片段合成复杂蛋白质. 这种醇-甲 (TSAL) 结策略促进了本源胺基键的产生,进步了蛋白质工程.