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Confined Diffusion Without Fences of a G-Protein-Coupled Receptor as Revealed by Single Particle Tracking

机译:如单粒子跟踪所揭示没有G蛋白偶联受体的栅栏的受限扩散。

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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 μ-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.
机译:单个粒子跟踪是探测质膜成分的组织和动力学的强大工具。我们使用这种技术来研究μ阿片受体,该阿片受体属于G蛋白偶联受体的大家族,与信号传导途径中的其他伙伴有关。在成纤维细胞中稳定表达的,在其N末端与T7-tag偶联的受体的特异性标记是通过与单克隆抗T7-tag抗体偶联的胶体金实现的。粒子的横向运动通过纳米视频显微镜在2分钟内以40毫秒的时间分辨率进行,其空间精度为15 nm。发现受体具有慢速或定向扩散模式(10%)或步行受限扩散模式(90%),该模式由长期随机扩散和短期受限扩散组成,对应于受限于其中的扩散一个本身会扩散的域。结果表明,该限制是由于膜蛋白之间的长期吸引所产生的有效谐波电位。提出了一个相互作用的膜蛋白扩散的简单模型,该模型解释了短期和长期扩散系数的域大小的变化。

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