Sowers A E, Hackenbrock C R
Proc Natl Acad Sci U S A. 1981 Oct;78(10):6246-50. doi: 10.1073/pnas.78.10.6246.
A method combining electrophoresis and freeze-fracture electron microscopy is described; the method was used to determine the lateral diffusion coefficient of intramembrane particles (integral proteins) in the mitochondrial inner membrane. An electric current was passed through microsuspensions of purified, spherical inner membranes at pH 7.4, which caused an electrophoretic migration of intramembrane particles in the membrane plane into a single, crowded patch facing the positive electrode. The membrane microsuspensions were quick-frozen at specified times after the packed particles were released from the electrophoretic force and while the particles were diffusing back to a random distribution. Observed concentration gradients of intramembrane particles during this time were quantitatively compared with and found to follow a mathematical model for Fickian diffusion of particles on a spherical membrane. The results determine the kinetics of free diffusion of integral proteins at the resolution of individual proteins. The diffusion coefficient of the integral proteins in the mitochondrial inner membrane was determined to be 8.3 X 10(-10) cm2/sec at 20 degrees C, from which a root-mean-square displacement of 57 nm in 10 msec is predicted.
本文描述了一种结合电泳和冷冻断裂电子显微镜的方法;该方法用于测定线粒体内膜中膜内颗粒(整合蛋白)的侧向扩散系数。在pH 7.4条件下,让电流通过纯化的球形内膜微悬浮液,这会导致膜内颗粒在膜平面内发生电泳迁移,形成一个朝向正极的单一、密集斑块。在堆积的颗粒从电泳力释放后且颗粒扩散回随机分布的特定时间,将膜微悬浮液快速冷冻。在此期间观察到的膜内颗粒浓度梯度与球形膜上颗粒的菲克扩散数学模型进行了定量比较,发现符合该模型。结果在单个蛋白质的分辨率下确定了整合蛋白自由扩散的动力学。在20℃时,线粒体内膜中整合蛋白的扩散系数测定为8.3×10⁻¹⁰ cm²/秒,据此预测在10毫秒内的均方根位移为57纳米。