变构调节
深度学习
蛋白质设计
合成生物学
计算机科学
计算生物学
人工智能
蛋白质结构
生物物理学
纳米技术
化学
生物
生物化学
受体
材料科学
作者
Amy B. Guo,Deniz Akpinaroglu,C. Stephens,Michael Grabe,Colin A. Smith,Mark J. S. Kelly,Tanja Kortemme
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2025-05-22
卷期号:388 (6749): eadr7094-eadr7094
被引量:59
标识
DOI:10.1126/science.adr7094
摘要
Deep learning has advanced the design of static protein structures, but the controlled conformational changes that are hallmarks of natural signaling proteins have remained inaccessible to de novo design. Here, we describe a general deep learning-guided approach for de novo design of dynamic changes between intradomain geometries of proteins, similar to switch mechanisms prevalent in nature, with atomic-level precision. We solve four structures that validate the designed conformations, demonstrate modulation of the conformational landscape by orthosteric ligands and allosteric mutations, and show that physics-based simulations are in agreement with deep-learning predictions and experimental data. Our approach demonstrates that new modes of motion can now be realized through de novo design and provides a framework for constructing biology-inspired, tunable, and controllable protein signaling behavior de novo.
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