Pöyry Sanja, Róg Tomasz, Karttunen Mikko, Vattulainen Ilpo
Institute of Physics, Tampere University of Technology, Finland, Faculty of Electrical Engineering, Helsinki University of Technology, Finland.
J Phys Chem B. 2008 Mar 13;112(10):2922-9. doi: 10.1021/jp7100495. Epub 2008 Feb 16.
Cholesterol is an indispensable molecule in mammalian cell membranes. To truly understand its role in the functions of membranes, it is essential to unravel cholesterol's structure-function relationship determined by underlying molecular interactions. For this purpose, we elaborate on this issue by considering the previously proposed idea that cholesterol's effects on a number of physical properties of membranes have been optimized during the evolution by removal of its excess methyl groups from the alpha-face of cholesterol, thus "smoothening" the structure. Consequently, the methyl groups still attached to cholesterol are one of the most intriguing structural features of the molecule. An obvious question arises: Why do these methyl groups still exist, and could cholesterol properties be further optimized by their removal? Because of the nature of the biosynthetic pathways of cholesterol, and the evidence of decreased interactions between sterols and lipid acyl chains when methyl groups are present, it seems plausible that removal of the methyl groups might indeed lead to stronger ordering and condensing effects of the cholesterol molecule. Atomic-scale molecular dynamics simulations of numerous modified sterols embedded in saturated lipid bilayers demonstrate, however, that the issue is more subtle. The analysis reveals a complex interplay between the lipid acyl chains and the structural details of cholesterol. Changes in cholesterol structure typically do not improve its performance in terms of promoting membrane order. This view is substantiated by a detailed analysis of the simulation data. In particular, it highlights the importance of the methyl group C18 for cholesterol properties. The C18 group resides between the third and fourth ring of cholesterol on its "rough" beta-side, and the results provide compelling evidence that C18 is crucial for the proper orientation of the sterol. More generally, the data provide insight into the role of the methyl groups of cholesterol.
胆固醇是哺乳动物细胞膜中不可或缺的分子。要真正理解其在膜功能中的作用,必须揭示由潜在分子相互作用决定的胆固醇结构 - 功能关系。为此,我们通过考虑先前提出的观点来阐述这个问题,即胆固醇对膜的许多物理性质的影响在进化过程中通过从胆固醇的α面去除其多余的甲基而得到优化,从而使结构“平滑”。因此,仍然连接在胆固醇上的甲基是该分子最引人入胜的结构特征之一。一个明显的问题出现了:为什么这些甲基仍然存在,去除它们是否可以进一步优化胆固醇的性质?由于胆固醇生物合成途径的性质,以及当存在甲基时甾醇与脂质酰基链之间相互作用减少的证据,去除甲基似乎确实可能导致胆固醇分子更强的有序化和凝聚作用。然而,对嵌入饱和脂质双层中的多种修饰甾醇的原子尺度分子动力学模拟表明,问题更为微妙。分析揭示了脂质酰基链与胆固醇结构细节之间的复杂相互作用。胆固醇结构的变化通常不会在促进膜有序方面提高其性能。对模拟数据的详细分析证实了这一观点。特别是,它突出了甲基C18对胆固醇性质的重要性。C18基团位于胆固醇“粗糙”β侧的第三和第四环之间,结果提供了令人信服的证据,表明C18对于甾醇的正确取向至关重要。更一般地说,这些数据提供了对胆固醇甲基作用的深入了解。