Departments of Molecular Genetics, Biochemistry and Chemistry, University of Toronto, Toronto, ON, Canada, M5S 1A8.
Proc Natl Acad Sci U S A. 2012 Nov 20;109(47):19268-73. doi: 10.1073/pnas.1212036109. Epub 2012 Nov 5.
Friction plays a critical role in protein folding. Frictional forces originating from random solvent and protein fluctuations both retard motion along the folding pathway and activate protein molecules to cross free energy barriers. Studies of friction thus may provide insights into the driving forces underlying protein conformational dynamics. However, the molecular origin of friction in protein folding remains poorly understood because, with the exception of the native conformer, there generally is little detailed structural information on the other states participating in the folding process. Here, we study the folding of the four-helix bundle FF domain that proceeds via a transiently formed, sparsely populated compact on-pathway folding intermediate whose structure was elucidated previously. Because the intermediate is stabilized by both native and nonnative interactions, friction in the folding transition between intermediate and folded states is expected to arise from intrachain reorganization in the protein. However, the viscosity dependencies of rates of folding from or unfolding to the intermediate, as established by relaxation dispersion NMR spectroscopy, clearly indicate that contributions from internal friction are small relative to those from solvent, so solvent frictional forces drive the folding process. Our results emphasize the importance of solvent dynamics in mediating the interconversion between protein configurations, even those that are highly compact, and in equilibrium folding/unfolding fluctuations in general.
摩擦在蛋白质折叠中起着关键作用。源自随机溶剂和蛋白质波动的摩擦力既会阻碍折叠途径中的运动,又会激活蛋白质分子跨越自由能势垒。因此,对摩擦力的研究可能有助于深入了解蛋白质构象动力学的驱动力。然而,由于除天然构象体外,其他参与折叠过程的状态通常很少有详细的结构信息,因此蛋白质折叠中摩擦力的分子起源仍未得到很好的理解。在这里,我们研究了四螺旋束 FF 结构域的折叠,该结构域通过一个短暂形成的、稀疏的紧凑的折叠中间体进行,该中间体的结构之前已经阐明。由于中间体是由天然和非天然相互作用稳定的,因此在中间体和折叠状态之间的折叠转变中摩擦力预计来自蛋白质内部的链内重组。然而,松弛分散 NMR 光谱学确定的从中性体折叠或去折叠的速率的粘度依赖性清楚地表明,与溶剂相比,内部摩擦力的贡献很小,因此溶剂摩擦力驱动折叠过程。我们的结果强调了溶剂动力学在介导蛋白质构象之间的相互转换,甚至是那些高度紧凑的构象以及一般的平衡折叠/去折叠波动中的重要性。