Institute for Integrated Cell-Material Sciences (iCeMS), Kyoto University, Kyoto 606-8507, Japan; Institute for Frontier Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
Institute for Integrated Cell-Material Sciences (iCeMS), Kyoto University, Kyoto 606-8507, Japan; Institute for Frontier Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
Curr Opin Cell Biol. 2014 Apr;27:78-86. doi: 10.1016/j.ceb.2013.11.008. Epub 2013 Dec 17.
Single fluorescent-molecule video imaging and tracking in living cells are revolutionizing our understanding of molecular interactions in the plasma membrane and intracellular membrane systems. They have revealed that molecular interactions occur surprisingly dynamically on much shorter time scales (≪1s) than those expected from the results by conventional techniques, such as pull-down assays (minutes to hours). Single-molecule imaging has unequivocally showed that G-protein-coupled receptors (GPCRs) undergo dynamic equilibrium between monomers and dimers, by enabling the determination of the 2D monomer-dimer equilibrium constant, the dimer dissociation rate constant (typically ∼10s(-1)), and the formation rate constant. Within one second, GPCRs typically undergo several cycles of monomer and homo-dimer formation with different partners.
活细胞中单荧光分子的视频成像和追踪正在彻底改变我们对质膜和细胞内膜系统中分子相互作用的理解。它们揭示了分子相互作用发生的时间尺度比传统技术(如下拉测定法,分钟到小时)所预期的要短得多(≪1s)。单分子成像明确表明,G 蛋白偶联受体(GPCR)在单体和二聚体之间处于动态平衡,这使得可以确定 2D 单体-二聚体平衡常数、二聚体解离速率常数(通常为 ∼10s(-1))和形成速率常数。在一秒钟内,GPCR 通常会与不同的伴侣经历几个单体和同源二聚体形成的循环。