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膜融合:以脂质囊泡为模型系统

Membrane fusion: lipid vesicles as a model system.

作者信息

Wilschut J, Hoekstra D

出版信息

Chem Phys Lipids. 1986 Jun-Jul;40(2-4):145-66. doi: 10.1016/0009-3084(86)90068-x.

Abstract

In many cellular functions the process of membrane fusion is of vital importance. It occurs in a highly specific and strictly controlled fashion. Proteins are likely to play a key role in the induction and modulation of membrane fusion reactions. Aimed at providing insight into the molecular mechanisms of membrane fusion, numerous studies have been carried out on model membrane systems. For example, the divalent-cation induced aggregation and fusion of vesicles consisting of negatively charged phospholipids, such as phosphatidylserine (PS) or cardiolipin (CL), have been characterized in detail. It is important to note that these systems largely lack specificity and control. Therefore conclusions derived from their investigation can not be extrapolated directly to a seemingly comparable counterpart in biology. Yet, the study of model membrane systems does reveal the general requirements of lipid bilayer fusion. The most prominent barrier to molecular contact between two apposing bilayers appears to be due to the hydration of the polar groups of the lipid molecules. Thus, dehydration of the bilayer surface and fluctuations in lipid packing, allowing direct hydrophobic interactions, are critical to the induction of membrane fusion. These membrane alterations are likely to occur only locally, at the site of intermembrane contact. Current views on the way membrane proteins may induce fusion under physiological conditions also emphasize the notion of local surface dehydration and perturbation of lipid packing, possibly through penetration of apolar amino acid segments into the hydrophobic membrane interior.

摘要

在许多细胞功能中,膜融合过程至关重要。它以高度特异性和严格受控的方式发生。蛋白质可能在膜融合反应的诱导和调节中起关键作用。为了深入了解膜融合的分子机制,人们对模型膜系统进行了大量研究。例如,已经详细表征了由带负电荷的磷脂(如磷脂酰丝氨酸(PS)或心磷脂(CL))组成的囊泡在二价阳离子诱导下的聚集和融合。需要注意的是,这些系统在很大程度上缺乏特异性和控制。因此,从它们的研究中得出的结论不能直接外推到生物学中看似类似的对应物。然而,对模型膜系统的研究确实揭示了脂质双层融合的一般要求。两个相对双层之间分子接触的最主要障碍似乎是由于脂质分子极性基团的水合作用。因此,双层表面的脱水和脂质堆积的波动,允许直接的疏水相互作用,对于膜融合的诱导至关重要。这些膜改变可能仅在膜间接触部位局部发生。目前关于膜蛋白在生理条件下可能诱导融合方式的观点也强调了局部表面脱水和脂质堆积扰动的概念,可能是通过非极性氨基酸片段渗透到疏水膜内部来实现的。

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