Department of Biochemistry and Structural Biology, University of Texas Health Science Center, San Antonio, TX 78229-3900, USA.
Int J Mol Sci. 2019 May 11;20(9):2334. doi: 10.3390/ijms20092334.
Hsp70s use ATP to generate forces that disassemble protein complexes and aggregates, and that translocate proteins into organelles. Entropic pulling has been proposed as a novel mechanism, distinct from the more familiar power-stroke and Brownian ratchet models, for how Hsp70s generate these forces. Experimental evidence supports entropic pulling, but this model may not be well understood among scientists studying these systems. In this review we address persistent misconceptions regarding the dynamics of proteins in solution that contribute to this lack of understanding, and we clarify the basic physics of entropic pulling with some simple analogies. We hope that increased understanding of the entropic pulling mechanism will inform future efforts to characterize how Hsp70s function as motors, and how they coordinate with their regulatory cochaperones in mechanochemical cycles that transduce the energy of ATP hydrolysis into physical changes in their protein substrates.
Hsp70s 使用 ATP 产生力,以拆散蛋白质复合物和聚集体,并将蛋白质转运到细胞器中。熵牵引被提议作为一种新颖的机制,与更熟悉的动力冲程和布朗棘轮模型不同,用于 Hsp70s 如何产生这些力。实验证据支持熵牵引,但在研究这些系统的科学家中,该模型可能还没有被很好地理解。在这篇综述中,我们解决了关于溶液中蛋白质动力学的持久误解,这些误解导致了对该模型的理解不足,并通过一些简单的类比澄清了熵牵引的基本物理学。我们希望对熵牵引机制的理解的提高将为未来的研究提供信息,这些研究旨在描述 Hsp70s 如何作为马达发挥作用,以及它们如何在机械化学循环中与调节伴侣蛋白协调,将 ATP 水解的能量转化为其蛋白质底物的物理变化。