Vrljic Marija, Nishimura Stefanie Y, Brasselet Sophie, Moerner W E, McConnell Harden M
Biophysics Program, Stanford University, Stanford, CA 94305-5080, USA.
Biophys J. 2002 Nov;83(5):2681-92. doi: 10.1016/S0006-3495(02)75277-6.
Single-molecule epifluorescence microscopy was used to observe the translational motion of GPI-linked and native I-E(k) class II MHC membrane proteins in the plasma membrane of CHO cells. The purpose of the study was to look for deviations from Brownian diffusion that might arise from barriers to this motion. Detergent extraction had suggested that these proteins may be confined to lipid microdomains in the plasma membrane. The individual I-E(k) proteins were visualized with a Cy5-labeled peptide that binds to a specific extracytoplasmic site common to both proteins. Single-molecule trajectories were used to compute a radial distribution of displacements, yielding average diffusion coefficients equal to 0.22 (GPI-linked I-E(k)) and 0.18 microm(2)/s (native I-E(k)). The relative diffusion of pairs of proteins was also studied for intermolecular separations in the range 0.3-1.0 microm, to distinguish between free diffusion of a protein molecule and diffusion of proteins restricted to a rapidly diffusing small domain. Both analyses show that motion is predominantly Brownian. This study finds no strong evidence for significant confinement of either GPI-linked or native I-E(k) in the plasma membrane of CHO cells.
利用单分子落射荧光显微镜观察了糖基磷脂酰肌醇(GPI)连接的和天然的I-E(k) II类主要组织相容性复合体(MHC)膜蛋白在CHO细胞膜中的平移运动。该研究的目的是寻找可能因这种运动的障碍而产生的与布朗扩散的偏差。去污剂提取表明这些蛋白质可能局限于质膜中的脂质微区。用与两种蛋白质共有的特定胞外位点结合的Cy5标记肽对单个I-E(k)蛋白进行可视化。利用单分子轨迹计算位移的径向分布,得出平均扩散系数分别为0.22(GPI连接的I-E(k))和0.18μm²/s(天然I-E(k))。还研究了分子间距离在0.3 - 1.0μm范围内的蛋白质对的相对扩散,以区分蛋白质分子的自由扩散和限制在快速扩散的小区域内的蛋白质扩散。两种分析均表明运动主要是布朗运动。该研究没有发现有力证据表明CHO细胞质膜中的GPI连接的或天然的I-E(k)受到显著限制。