激发态
离解(化学)
信号
化学物理
计算机科学
合理设计
化学
动力学
生物物理学
细胞因子受体
生物系统
亚稳态
信号通路
蛋白质动力学
设计要素和原则
蛋白质设计
基态
细胞因子
光谱学
分子动力学
血浆蛋白结合
纳米技术
费斯特共振能量转移
蛋白质结构
HEK 293细胞
结合位点
能源景观
蛋白质-蛋白质相互作用
分子生物物理学
受体
系统生物学
作者
Adam J. Broerman,Christoph Pollmann,Yang Zhao,Mauriz A. Lichtenstein,Mark D. Jackson,Maxx H. Tessmer,Won Hee Ryu,Masato Ogishi,Mohamad H. Abedi,Danny D. Sahtoe,Aza Allen,Alex Kang,Joshmyn De La Cruz,Evans Brackenbrough,Banumathi Sankaran,Asim K. Bera,Daniel M. Zuckerman,Stefan Stoll,K. Christopher García,Florian Praetorius
出处
期刊:Nature
[Nature Portfolio]
日期:2025-09-24
卷期号:647 (8089): 528-535
被引量:29
标识
DOI:10.1038/s41586-025-09549-z
摘要
Abstract Protein design has focused on the design of ground states, ensuring that they are sufficiently low energy to be highly populated 1 . Designing the kinetics and dynamics of a system requires, in addition, the design of excited states that are traversed in transitions from one low-lying state to another 2,3 . This is a challenging task because such states must be sufficiently strained to be poorly populated, but not so strained that they are not populated at all, and because protein design methods have focused on generating near-ideal structures 4–7 . Here we describe a general approach for designing systems that use an induced-fit power stroke 8 to generate a structurally frustrated 9 and strained excited state, allosterically driving protein complex dissociation. X-ray crystallography, double electron–electron resonance spectroscopy and kinetic binding measurements show that incorporating excited states enables the design of effector-induced increases in dissociation rates as high as 5,700-fold. We highlight the power of this approach by designing rapid biosensors, kinetically controlled circuits and cytokine mimics that can be dissociated from their receptors within seconds, enabling dissection of the temporal dynamics of interleukin-2 signalling.
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