Saxton M J
Institute of Theoretical Dynamics, University of California, Davis 95616, USA.
Biophys J. 1995 Aug;69(2):389-98. doi: 10.1016/S0006-3495(95)79911-8.
Structural proteins of the membrane skeleton are thought to form "corrals" at the membrane surface, and these corrals may restrict lateral diffusion of membrane proteins. Recent experimental developments in single-particle tracking and laser trapping make it possible to examine the corral model in detail. Techniques to interpret these experiments are presented. First, escape times for a diffusing particle in a corral are obtained from Monte Carlo calculations and analytical solutions for various corral sizes, shapes, and escape probabilities, and reduced to a common curve. Second, the identification of corrals in tracking experiments is considered. The simplest way to identify corrals is by sight. If the walls are impermeable enough, a trajectory fills the corral before the diffusing particle escapes. The fraction of distinct sites visited before escape is calculated for corrals of various sizes, shapes, and escape probabilities, and reduced to a common curve. This fraction is also a measure of the probability that the diffusing species will react with another species in the corral before escaping. Finally, the effect of the sampling interval on the measurement of the short-range diffusion coefficient is examined.
膜骨架的结构蛋白被认为在膜表面形成“围栏”,并且这些围栏可能会限制膜蛋白的侧向扩散。单粒子追踪和激光捕获技术的最新实验进展使得详细研究围栏模型成为可能。本文介绍了解释这些实验的技术。首先,通过蒙特卡罗计算和针对各种围栏尺寸、形状和逃逸概率的解析解,获得扩散粒子在围栏中的逃逸时间,并将其简化为一条通用曲线。其次,考虑在追踪实验中识别围栏的方法。识别围栏最简单的方法是目视观察。如果围栏壁的渗透性足够低,扩散粒子在逃逸之前,其轨迹会填满整个围栏。针对各种尺寸、形状和逃逸概率的围栏,计算逃逸前访问的不同位点的比例,并将其简化为一条通用曲线。这个比例也是扩散物种在逃逸前与围栏内另一个物种发生反应的概率的一种度量。最后,研究了采样间隔对短程扩散系数测量的影响。