Olveczky B P, Verkman A S
Department of Medicine, Cardiovascular Research Institute, University of California, San Francisco 94143, USA.
Biophys J. 1998 May;74(5):2722-30. doi: 10.1016/S0006-3495(98)77978-0.
Molecular transport in the aqueous lumen of organelles involves diffusion in a confined compartment with complex geometry. Monte Carlo simulations of particle diffusion in three dimensions were carried out to evaluate the influence of organelle structure on diffusive transport and to relate experimental photobleaching data to intrinsic diffusion coefficients. Two organelle structures were modeled: a mitochondria-like long closed cylinder containing fixed luminal obstructions of variable number and size, and an endoplasmic reticulum-like network of interconnected cylinders of variable diameter and density. Trajectories were computed in each simulation for >10(5) particles, generally for >10(5) time steps. Computed time-dependent concentration profiles agreed quantitatively with analytical solutions of the diffusion equation for simple geometries. For mitochondria-like cylinders, significant slowing of diffusion required large or wide single obstacles, or multiple obstacles. In simulated spot photobleaching experiments, a approximately 25% decrease in apparent diffusive transport rate (defined by the time to 75% fluorescence recovery) was found for a single thin transverse obstacle occluding 93% of lumen area, a single 53%-occluding obstacle of width 16 lattice points (8% of cylinder length), 10 equally spaced 53% obstacles alternately occluding opposite halves of the cylinder lumen, or particle binding to walls (with mean residence time = 10 time steps). Recovery curve shape with obstacles showed long tails indicating anomalous diffusion. Simulations also demonstrated the utility of measurement of fluorescence depletion at a spot distant from the bleach zone. For a reticulum-like network, particle diffusive transport was mildly reduced from that in unobstructed three-dimensional space. In simulated photobleaching experiments, apparent diffusive transport was decreased by 39-60% in reticular structures in which 90-97% of space was occluded. These computations provide an approach to analyzing photobleaching data in terms of microscopic diffusive properties and support the paradigm that organellar barriers must be quite severe to seriously impede solute diffusion.
细胞器水相腔中的分子运输涉及在具有复杂几何形状的受限隔室内的扩散。进行了三维粒子扩散的蒙特卡罗模拟,以评估细胞器结构对扩散运输的影响,并将实验光漂白数据与固有扩散系数相关联。对两种细胞器结构进行了建模:一种是类似线粒体的长封闭圆柱体,包含数量和大小可变的固定腔内障碍物;另一种是类似内质网的由直径和密度可变的相互连接的圆柱体组成的网络。在每个模拟中,为超过10⁵个粒子计算轨迹,通常计算超过10⁵个时间步长。计算得到的随时间变化的浓度分布与简单几何形状扩散方程的解析解在数量上一致。对于类似线粒体的圆柱体,扩散的显著减慢需要大的或宽的单个障碍物,或多个障碍物。在模拟的点光漂白实验中,对于一个阻塞93%腔面积的单个薄横向障碍物、一个宽度为16个晶格点(圆柱体长度的8%)阻塞53%的单个障碍物、10个等间距交替阻塞圆柱体腔相对两半的53%障碍物,或粒子与壁结合(平均停留时间 = 10个时间步长),发现表观扩散运输速率(由75%荧光恢复时间定义)大约降低25%。有障碍物时恢复曲线形状显示出长尾巴,表明存在反常扩散。模拟还证明了在远离漂白区的一个点测量荧光消耗的实用性。对于类似网状的网络,粒子扩散运输比在无阻碍的三维空间中略有降低。在模拟光漂白实验中,在90 - 97%的空间被阻塞网状结构中,表观扩散运输降低了39 - 60%。这些计算提供了一种根据微观扩散特性分析光漂白数据的方法,并支持这样一种范式,即细胞器屏障必须相当严重才能严重阻碍溶质扩散。