Ji Tuo, Ge Piao, Zhang Shan, Wan Chanjuan, Liu Hailong, Qu Xiaozhan, Zhu Feng, Gong Qingguo, Xu Weiya, Wang Chao, Wang Yucai, Huang Chengdong
Ministry of Education Key Laboratory for Membrane-less Organelles and Cellular Dynamics, Center for Advanced Interdisciplinary Science and Biomedicine of IHM, Biomedical Sciences and Health Laboratory of Anhui Province, Hefei National Laboratory for Physical Sciences at the Microscale, School of Life Sciences, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, P. R. China.
Nat Struct Mol Biol. 2025 Jun 4. doi: 10.1038/s41594-025-01585-7.
While the regulation of protein function theoretically encompasses alterations in both structural conformation and dynamic properties, the latter aspect, specifically conformational entropy, remains relatively unexplored. Here we show that an intrinsically disordered region (IDR), a prominent component of the proteome, can remotely switch protein activity on or off through a nonbinding, entropy-driven mechanism. Focusing on the disordered C-terminal tail of Sgt2, a chaperone in the guided entry of tail-anchored protein pathway, we demonstrate that it allosterically inhibits the N-terminal domain without direct contact, preventing unproductive chaperone-chaperone interactions. This inhibition is relieved upon client binding. These effects depend on specific IDR sequences but not the intervening regions. Beyond acting as a relay signal, the IDR also forms a dynamic complex with transmembrane domains of tail-anchored clients, serving as an entropic shelter. Moreover, the IDR-mediated activity of Sgt2 correlates with fast internal dynamics, establishing conformational entropy as a key regulatory principle. Our findings reveal IDRs as two-way entropic modulators, enabling distant, on-demand activity switching.
虽然理论上蛋白质功能的调节包括结构构象和动力学性质的改变,但后一个方面,特别是构象熵,仍相对未被探索。在这里,我们表明,内在无序区域(IDR)作为蛋白质组的一个突出组成部分,可以通过一种非结合的、熵驱动的机制远程开启或关闭蛋白质活性。以尾锚定蛋白途径引导进入中的伴侣蛋白Sgt2的无序C末端尾巴为重点,我们证明它在不直接接触的情况下变构抑制N末端结构域,防止无生产性的伴侣蛋白-伴侣蛋白相互作用。这种抑制在与客户结合后解除。这些效应取决于特定的IDR序列,而不是中间区域。除了作为一种中继信号外,IDR还与尾锚定客户的跨膜结构域形成动态复合物,作为一个熵庇护所。此外,Sgt2的IDR介导的活性与快速的内部动力学相关,确立了构象熵作为一个关键的调节原则。我们的发现揭示了IDR是双向熵调节剂,能够实现远距离的、按需的活性切换。