Department of Chemical and Structural Biology, Weizmann Institute of Science, Rehovot 7610001, Israel.
Proc Natl Acad Sci U S A. 2022 Nov 29;119(48):e2213170119. doi: 10.1073/pnas.2213170119. Epub 2022 Nov 21.
Confining compartments are ubiquitous in biology, but there have been few experimental studies on the thermodynamics of protein folding in such environments. Recently, we reported that the stability of a model protein substrate in the GroEL/ES chaperonin cage is reduced dramatically by more than 5 kcal mol compared to that in bulk solution, but the origin of this effect remained unclear. Here, we show that this destabilization is caused, at least in part, by a diminished hydrophobic effect in the GroEL/ES cavity. This reduced hydrophobic effect is probably caused by water ordering due to the small number of hydration shells between the cavity and protein substrate surfaces. Hence, encapsulated protein substrates can undergo a process similar to cold denaturation in which unfolding is promoted by ordered water molecules. Our findings are likely to be relevant to encapsulated substrates in chaperonin systems, in general, and are consistent with the iterative annealing mechanism of action proposed for GroEL/ES.
在生物学中,局限隔室无处不在,但对于此类环境中蛋白质折叠的热力学,仅有少数实验研究。最近,我们报告称,与在本体溶液中相比,模型蛋白质底物在 GroEL/ES 伴侣蛋白笼中的稳定性显著降低超过 5 kcal/mol,但该效应的起源仍不清楚。在这里,我们表明,这种失稳至少部分是由 GroEL/ES 腔中疏水性降低引起的。这种疏水性降低可能是由于腔与蛋白质底物表面之间的水合壳数量较少而导致的水分子有序化引起的。因此,被包裹的蛋白质底物可以经历类似于冷变性的过程,其中展开是由有序水分子促进的。我们的发现可能与伴侣蛋白系统中的包裹底物有关,并且与 GroEL/ES 提出的迭代退火作用机制一致。