Yang Yi, Lin Shixian, Lin Wei, Chen Peng R
Synthetic and Functional Biomolecules Center, College of Chemistry and Molecular Engineering, Peking University, 202, Chengfu Road, Beijing 100871 (China).
Chembiochem. 2014 Aug 18;15(12):1738-43. doi: 10.1002/cbic.201400057. Epub 2014 May 8.
We have developed a dual-site click labeling strategy for the simultaneous installation of a FRET donor-acceptor pair onto the extracellular domains of epidermal growth factor receptor (EGFR) on living cells. Our method integrates the genetic code expansion strategy, enzyme-mediated protein labeling, and ligand-assisted Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) into a tri-step labeling procedure. This enabled cis-membrane FRET imaging of EGFR under living conditions. This procedure might be generally applicable for dual-site labeling and cis-membrane FRET analysis of the domain-domain dynamics of important mammalian cell-surface receptors.
我们开发了一种双位点点击标记策略,用于在活细胞的表皮生长因子受体(EGFR)胞外结构域上同时安装一对荧光共振能量转移(FRET)供体-受体。我们的方法将遗传密码扩展策略、酶介导的蛋白质标记以及配体辅助的铜(I)催化叠氮化物-炔烃环加成反应(CuAAC)整合到一个三步标记程序中。这使得在活细胞条件下对EGFR进行跨膜FRET成像成为可能。该程序可能普遍适用于重要哺乳动物细胞表面受体的结构域-结构域动力学的双位点标记和跨膜FRET分析。