Confined diffusion without fences of a G-protein-coupled receptor as revealed by single particle tracking

被引:161
作者
Daumas, F
Destainville, N
Millot, C
Lopez, A
Dean, D
Salomé, L
机构
[1] Inst Pharmacol & Biol Struct, CNRS, UMR 5089, F-31077 Toulouse, France
[2] IRSAMC, CNRS, UMR 5626, Phys Quant Lab, F-31064 Toulouse, France
关键词
D O I
10.1016/S0006-3495(03)74856-5
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Single particle tracking is a powerful tool for probing the organization and dynamics of the plasma membrane, constituents. We used this technique to study the mu-opioid receptor belonging to the large family of the G-protein-coupled receptors involved with other partners in a signal transduction pathway. The specific labeling of the receptor coupled to a T7-tag at its N-terminus, stably expressed in fibroblastic cells, was achieved by colloidal gold coupled to a monoclonal anti T7-tag antibody. The lateral movements of the particles were followed by nanovideomicroscopy at 40 ms time resolution during 2 min with a spatial precision of 15 nm. The receptors were found to have either a slow or directed diffusion mode (10%) or a walking confined diffusion mode (90%) composed of a long-term random diffusion and a short-term confined diffusion, and corresponding to a diffusion confined within a domain that itself diffuses. The results indicate that the confinement is due to an effective harmonic potential generated by long-range attraction between the membrane proteins. A simple model for interacting membrane proteins diffusion is proposed that explains the variations with the domain size of the short-term and long-term diffusion coefficients.
引用
收藏
页码:356 / 366
页数:11
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