Malinin Vladimir S, Frederik Peter, Lentz Barry R
Department of Biochemistry and Biophysics, CB#7260, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7260, USA.
Biophys J. 2002 Apr;82(4):2090-100. doi: 10.1016/S0006-3495(02)75556-2.
Poly (ethylene glycol) (PEG) in the external environment of membrane vesicles creates osmotic imbalance that leads to mechanical stress in membranes and may induce local membrane curvature. To determine the relative importance of membrane stress and curvature in promoting fusion, we monitored contents mixing (CM) and lipid mixing (LM) between different sized vesicles under a variety of osmotic conditions. CM between highly curved vesicles (SUV, 26 nm diameter) was up to 10 times greater than between less curved vesicles (LUV, 120 nm diameter) after 5 min incubation at a low PEG concentration (<10 wt%), whereas LM was only approximately 30% higher. Cryo-electron microscopy showed that PEG at 10 wt% did not create high curvature contacts between membranes in LUV aggregates. A negative osmotic gradient (-300 mOs/kg, hypotonic inside) increased CM two- to threefold for both types of vesicles, but did not affect LM. A positive gradient (+220 mOs/kg, hypertonic inside) nearly eliminated CM and had no effect on LM. Hexadecane added to vesicles had no effect on LM but enhanced CM and reduced the inhibitory effect on CM of a positive osmotic gradient, but had little influence on results obtained under a negative osmotic gradient. We conclude that the ability of closely juxtaposed bilayers to form an initial intermediate ("stalk") as soon as they come into close contact was not influenced by osmotic stress or membrane curvature, although pore formation was critically dependent on these stresses. The results also suggest that hexadecane affects the same part of the fusion process as osmotic stress. We interpret this result to suggest that both a negative osmotic gradient and hexadecane reduce the unfavorable free energy of hydrophobic interstices associated with the intermediates of the fusion process.
膜泡外部环境中的聚乙二醇(PEG)会造成渗透失衡,导致膜内产生机械应力,并可能引发局部膜曲率变化。为了确定膜应力和曲率在促进融合过程中的相对重要性,我们监测了在各种渗透条件下不同大小囊泡之间的内容物混合(CM)和脂质混合(LM)情况。在低PEG浓度(<10 wt%)下孵育5分钟后,高度弯曲的囊泡(SUV,直径26 nm)之间的CM比弯曲程度较小的囊泡(LUV,直径120 nm)之间的CM高出多达10倍,而LM仅高出约30%。冷冻电子显微镜显示,10 wt%的PEG不会在LUV聚集体的膜之间形成高曲率接触。负渗透梯度(-300 mOs/kg,内部为低渗)使两种类型囊泡的CM增加了两到三倍,但对LM没有影响。正梯度(+220 mOs/kg,内部为高渗)几乎消除了CM,对LM没有影响。添加到囊泡中的十六烷对LM没有影响,但增强了CM,并降低了正渗透梯度对CM的抑制作用,但对负渗透梯度下获得的结果影响很小。我们得出结论,紧密并列的双层膜一旦紧密接触就形成初始中间体(“茎”)的能力不受渗透应力或膜曲率的影响,尽管孔的形成严重依赖于这些应力。结果还表明,十六烷与渗透应力影响融合过程的同一部分。我们将这一结果解释为,负渗透梯度和十六烷都降低了与融合过程中间体相关的疏水间隙的不利自由能。