丙氨酸扫描
丙氨酸
肽
蛋白质-蛋白质相互作用
残留物(化学)
化学
配体(生物化学)
组合化学
生物化学
蛋白质设计
蛋白质结构
计算生物学
立体化学
生物
氨基酸
受体
突变
基因
突变
作者
Xiyun Ye,Yen-Chun Lee,Zachary P. Gates,Yingjie Ling,Jennifer Gaines,Fan-Shen Yang,Yu-Shan Lin,Bradley L. Pentelute
标识
DOI:10.1038/s42004-022-00737-w
摘要
Establishing structure-activity relationships is crucial to understand and optimize the activity of peptide-based inhibitors of protein-protein interactions. Single alanine substitutions provide limited information on the residues that tolerate simultaneous modifications with retention of biological activity. To guide optimization of peptide binders, we use combinatorial peptide libraries of over 4,000 variants-in which each position is varied with either the wild-type residue or alanine-with a label-free affinity selection platform to study protein-ligand interactions. Applying this platform to a peptide binder to the oncogenic protein MDM2, several multi-alanine-substituted analogs with picomolar binding affinity were discovered. We reveal a non-additive substitution pattern in the selected sequences. The alanine substitution tolerances for peptide ligands of the 12ca5 antibody and 14-3-3 regulatory protein are also characterized, demonstrating the general applicability of this new platform. We envision that binary combinatorial alanine scanning will be a powerful tool for investigating structure-activity relationships.
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