Division of Physical Biochemistry, Medical Research Council National Institute for Medical Research, London NW7 1AA, United Kingdom.
Proc Natl Acad Sci U S A. 2010 Feb 9;107(6):2693-8. doi: 10.1073/pnas.0907915107. Epub 2010 Jan 20.
G-protein-coupled receptors (GPCRs) are the largest family of transmembrane signaling proteins in the human genome. Events in the GPCR signaling cascade have been well characterized, but the receptor composition and its membrane distribution are still generally unknown. Although there is evidence that some members of the GPCR superfamily exist as constitutive dimers or higher oligomers, interpretation of the results has been disputed, and recent studies indicate that monomeric GPCRs may also be functional. Because there is controversy within the field, to address the issue we have used total internal reflection fluorescence microscopy (TIRFM) in living cells to visualize thousands of individual molecules of a model GPCR, the M(1) muscarinic acetylcholine receptor. By tracking the position of individual receptors over time, their mobility, clustering, and dimerization kinetics could be directly determined with a resolution of approximately 30 ms and approximately 20 nm. In isolated CHO cells, receptors are randomly distributed over the plasma membrane. At any given time, approximately 30% of the receptor molecules exist as dimers, and we found no evidence for higher oligomers. Two-color TIRFM established the dynamic nature of dimer formation with M(1) receptors undergoing interconversion between monomers and dimers on the timescale of seconds.
G 蛋白偶联受体 (GPCR) 是人类基因组中最大的跨膜信号蛋白家族。GPCR 信号级联事件已得到很好的描述,但受体组成及其膜分布仍普遍未知。尽管有证据表明 GPCR 超家族的一些成员作为组成型二聚体或更高寡聚体存在,但对结果的解释存在争议,最近的研究表明单体 GPCR 也可能具有功能。由于该领域存在争议,为了解决这个问题,我们在活细胞中使用全内反射荧光显微镜 (TIRFM) 来可视化模型 GPCR(M1 毒蕈碱乙酰胆碱受体)的数千个单个分子。通过随时间跟踪单个受体的位置,可以直接确定其流动性、聚类和二聚化动力学,分辨率约为 30 毫秒和约 20 纳米。在分离的 CHO 细胞中,受体随机分布在质膜上。在任何给定的时间,大约 30%的受体分子作为二聚体存在,我们没有发现更高寡聚体的证据。双色 TIRFM 证实了 M1 受体之间的二聚体形成的动态性质,二聚体在秒的时间尺度上在单体和二聚体之间相互转化。