Risselada Herre Jelger, Bubnis Gregory, Grubmüller Helmut
Theoretical and Computational Biophysics Department, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany; andLeibniz Institute of Surface Modification, D-04318 Leipzig, Germany
Theoretical and Computational Biophysics Department, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany; and.
Proc Natl Acad Sci U S A. 2014 Jul 29;111(30):11043-8. doi: 10.1073/pnas.1323221111. Epub 2014 Jul 14.
Over the past 20 years, it has been widely accepted that membrane fusion proceeds via a hemifusion step before opening of the productive fusion pore. An initial hourglass-shaped lipid structure, the fusion stalk, is formed between the adjacent membrane leaflets (cis leaflets). It remains controversial if and how fusion proteins drive the subsequent transition (expansion) of the stalk into a fusion pore. Here, we propose a comprehensive and consistent thermodynamic understanding in terms of the underlying free-energy landscape of stalk expansion. We illustrate how the underlying free energy landscape of stalk expansion and the concomitant pathway is altered by subtle differences in membrane environment, such as leaflet composition, asymmetry, and flexibility. Nonleaky stalk expansion (stalk widening) requires the formation of a critical trans-leaflet contact. The fusion machinery can mechanically enforce trans-leaflet contact formation either by directly enforcing the trans-leaflets in close proximity, or by (electrostatically) condensing the area of the cis leaflets. The rate of these fast fusion reactions may not be primarily limited by the energetics but by the forces that the fusion proteins are able to exert.
在过去20年里,人们普遍认为膜融合在形成有功能的融合孔之前会经过一个半融合步骤。最初会在相邻的膜小叶(顺式小叶)之间形成一个沙漏状的脂质结构,即融合柄。融合蛋白是否以及如何驱动融合柄随后转变(扩张)为融合孔仍存在争议。在此,我们基于融合柄扩张潜在的自由能态势,提出了一种全面且一致的热力学理解。我们阐述了膜环境中的细微差异,如小叶组成、不对称性和柔韧性,是如何改变融合柄扩张的潜在自由能态势及相应途径的。无泄漏的融合柄扩张(柄变宽)需要形成关键的反式小叶接触。融合机制可以通过直接使反式小叶紧密靠近,或者通过(静电)压缩顺式小叶的面积,来机械地促使反式小叶接触的形成。这些快速融合反应的速率可能主要不受能量学限制,而是受融合蛋白能够施加的力的限制。