蛋白质工程
蛋白质设计
计算生物学
细胞因子
受体
白细胞介素2
蛋白质结构
细胞生物学
合成生物学
血浆蛋白结合
化学
生物
生物化学
免疫学
酶
作者
Junming Ren,Alexander E. Chu,Kevin M. Jude,Lora K. Picton,Aris J. Kare,Leon Su,Alejandra Montano Romero,Po‐Ssu Huang,K. Christopher García
标识
DOI:10.1073/pnas.2117401119
摘要
Significance While computational engineering of therapeutic proteins is a desirable goal, in practice the optimization of protein–protein interactions requires substantial experimental intervention. We present here a computational approach that focuses on stabilizing core protein structures rather than engineering the protein–protein interface. Using this approach, we designed thermostabilized interleukin-2 (IL-2) variants that bind tightly to their receptor without experimental optimization, mimicking the properties of the yeast-display engineered IL-2 variant “super-2.” Our results suggest that structure-guided stabilization may be a general method for in silico affinity maturation of protein–protein interactions.
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