李文斐
Professor Supervisor of Doctorate Candidates Supervisor of Master's Candidates
Name (Simplified Chinese):李文斐
E-Mail:
Date of Employment:2021-02
School/Department:Shandong University, School of Basic Medical Sciences
Administrative Position:Professor
Education Level:Postgraduate (Postdoctoral)
Business Address:School of Basic Medical Sciences, Shandong University
Gender:Female
Contact Information:
Degree:Doctor
Academic Titles:医学结构生物学中心副主任
Alma Mater:Tsinghua University
College:School of Basic Medical Sciences
Discipline:Biochemistry and Molecular Biology
Cell Biology
Biophysics
Genetics
Honor
2022 BMS本科生优秀班主任
2022 泰山学者青年专家
2021 齐鲁青年学者(第一层次)
2022 山东省优秀青年(海外)
2015 北京市优秀毕业生
2009 北京市大学生科学研究与创业
2015 博士生毕业论文奖
国家奖学金
2013 清华大学学生实验室建设贡献二等奖
Hits:
Title of Paper:A simplified and highly efficient cell-free protein synthesis system for prokaryotes
Journal:eLife
Summary:Cell-free protein synthesis (CFPS) systems are a powerful platform with immense potential in fundamental research, biotechnology, and synthetic biology. Conventional prokaryotic CFPS systems, particularly those derived from Escherichia coli (E. coli), often rely on complex reaction buffers containing up to thirty-five components, limiting their widespread adoption and systematic optimization. Here, we present an optimized E. coli cell-free protein synthesis (eCFPS) system, which is significantly streamlined for high efficiency. Through systematic screening, we successfully reduced the essential core reaction components from 35 to a core set of 7. The thorough optimization of these seven key components ensured that protein expression levels were not only maintained but even substantially improved. Furthermore, we developed a much simpler procedure for preparing the bacterial cytosolic extracts, a “fast lysate” protocol that eliminates the traditional time-consuming runoff and dialysis steps, thereby enhancing the overall accessibility and robustness of eCFPS. This optimized and user-friendly eCFPS efficiently synthesizes challenging proteins, including functional, self-assembling vimentin, and active restriction endonuclease BsaI despite its strong cytotoxicity, and serves as a powerful tool that will facilitate diverse applications in basic life science research and beyond.
DOI Number:10.7554/eLife.109495.1
Translation or Not:No
Date of Publication:2025-12
Links to Published Journals:https://elifesciences.org/reviewed-preprints/109495
Release Time:2026-03-18