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分泌过程中作用于融合孔膜的力和应力。

Forces and stresses acting on fusion pore membrane during secretion.

作者信息

Tajparast M, Glavinović M I

机构信息

Department of Civil Engineering, McGill University, Montreal, PQ, Canada.

出版信息

Biochim Biophys Acta. 2009 May;1788(5):1009-23. doi: 10.1016/j.bbamem.2009.01.019. Epub 2009 Feb 11.

DOI:10.1016/j.bbamem.2009.01.019
PMID:19366587
Abstract

To assess the forces and stresses present in fusion pore during secretion the stationary convective flux of lipid through a fusion pore connecting two planar membranes under different tensions was investigated through computer simulations. The physics of the problem is described by Navier-Stokes equations, and the convective flux of lipid was evaluated using finite element method. Each of the membrane monolayer is considered separately as an isotropic, homogeneous and incompressible viscous medium with the same viscosity. The difference in membrane tensions, which is simulated as the pressure difference at two ends of each monolayer, is the driving force of the lipid flow. The two monolayers interact by sliding past each other with inter-monolayer frictional viscosity. Fluid velocity, pressure, shear and normal stresses, viscous and frictional dissipations and forces were calculated to evaluate where the fusion pore will deform, extend (or compress) and dilate. The pressure changes little in the planar sections, whereas in the toroidal section the change is rapid. The magnitude of lipid velocity peaks at the pore neck. The radial lipid velocity is zero at the neck, has two peaks one on each side of the pore neck, and diminishes without going to zero in planar parts of two monolayers. The peaks are of opposite signs due to the change of direction of lipid flow. The axial velocity is confined to the toroidal section, peaks at the neck and is clearly greater in the outer monolayer. As a result of the spatially highly uneven lipid flow the membrane is under a significant stress, shear and normal. The shear stress, which indicates where the membrane will deform without changing the volume, has two peaks placed symmetrically about the neck. The normal stress shows where the membrane may extend or compress. Both, the radial and axial normal stresses are negative (extensive) in the upper toroidal section and positive (compressive) in the lower toroidal section. The pressure difference determines lipid velocity and velocity dependent variables (shear as well as normal axial and radial stresses), but also contributes directly to the force on the membranes and critically influences where and to what extent the membrane will deform, extend or dilate. The viscosity coefficient (due to friction of one element of lipid against neighboring ones), and frictional coefficient (due to friction between two monolayers sliding past each other) further modulate some variables. Lipid velocity rises as pressure difference increases, diminishes as the viscosity coefficient rises but is unaffected by the frictional coefficient. The shear and normal stresses rise as pressure difference increases, but the change of the viscosity coefficients has no effect. Both the viscous dissipation (which has two peaks placed symmetrically about the neck) and much smaller frictional dissipation (which peaks at the pore neck) rise with pressure and diminish if the viscosity coefficient rises, but only the frictional dissipation increases if the frictional coefficient increases. Finally, the radial force causing pore dilatation, and which is significant only in the planar section of the vesicular membrane, is governed almost entirely by the pressure, whereas the viscosity and frictional coefficients have only a marginal effect. Many variables are altered during pore dilatation. The lipid velocity and dissipations (viscous and frictional) rise approximately linearly with pore radius, whereas the lipid mass flow increases supra-linearly owing to the combined effects of the changes in pore radius and greater lipid velocity. Interestingly the radial force on the vesicular membrane increases only marginally.

摘要

为了评估分泌过程中融合孔内存在的力和应力,通过计算机模拟研究了在不同张力下,脂质通过连接两个平面膜的融合孔的稳态对流通量。该问题的物理过程由纳维 - 斯托克斯方程描述,脂质的对流通量使用有限元方法进行评估。每个膜单层分别被视为具有相同粘度的各向同性、均匀且不可压缩的粘性介质。膜张力的差异,模拟为每个单层两端的压力差,是脂质流动的驱动力。两个单层通过具有层间摩擦粘度的相互滑动而相互作用。计算流体速度、压力、剪切应力和法向应力、粘性和摩擦耗散以及力,以评估融合孔将在何处变形、延伸(或压缩)和扩张。在平面部分压力变化很小,而在环形部分变化迅速。脂质速度的大小在孔颈处达到峰值。径向脂质速度在孔颈处为零,在孔颈两侧各有一个峰值,并且在两个单层的平面部分不会降至零。由于脂质流动方向的改变,这些峰值具有相反的符号。轴向速度局限于环形部分,在孔颈处达到峰值,并且在外层单层中明显更大。由于脂质流动在空间上高度不均匀,膜承受着显著的应力、剪切应力和法向应力。剪切应力表明膜将在何处变形而不改变体积,在孔颈两侧对称地有两个峰值。法向应力表明膜可能延伸或压缩的位置。径向和轴向法向应力在上部环形部分均为负(拉伸),在下部环形部分为正(压缩)。压力差决定脂质速度和与速度相关的变量(剪切应力以及轴向和径向法向应力),但也直接作用于膜上的力,并严重影响膜将在何处以及在多大程度上变形、延伸或扩张。粘度系数(由于脂质的一个元素与相邻元素之间的摩擦)和摩擦系数(由于两个单层相互滑动时的摩擦)进一步调节一些变量。脂质速度随着压力差的增加而上升,随着粘度系数的上升而降低,但不受摩擦系数的影响。剪切应力和法向应力随着压力差的增加而上升,但粘度系数的变化没有影响。粘性耗散(在孔颈两侧对称地有两个峰值)和小得多的摩擦耗散(在孔颈处达到峰值)都随着压力的增加而上升,如果粘度系数上升则降低,但只有摩擦耗散在摩擦系数增加时会增加。最后,导致孔扩张的径向力,仅在囊泡膜的平面部分显著,几乎完全由压力控制,而粘度和摩擦系数只有边际效应。在孔扩张过程中许多变量会发生变化。脂质速度和耗散(粘性和摩擦)随孔半径近似线性上升,而脂质质量流由于孔半径变化和更大的脂质速度的综合作用而超线性增加。有趣的是,囊泡膜上的径向力仅略有增加。

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