首页> 外文期刊>Current Opinion in Cell Biology >Single-molecule imaging revealed dynamic GPCR dimerization. [Review][Erratum appears in Curr Opin Cell Biol. 2014 Apr;27:144]
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Single-molecule imaging revealed dynamic GPCR dimerization. [Review][Erratum appears in Curr Opin Cell Biol. 2014 Apr;27:144]

机译:单分子成像显示动态GPCR二聚化。 [综述] [勘误出现在Curr Opin Cell Biol中。 2014 Apr; 27:144]

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摘要

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
机译:活细胞中的单个荧光分子视频成像和跟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。他们已经发现,与传统技术(例如下拉法(几分钟到几小时))的结果相比,分子相互作用出奇地动态地发生在更短的时间尺度( 1s)上。单分子成像明确表明,通过确定2D单体-二聚体平衡常数,二聚体解离速率常数(通常约为10s(-1),G蛋白偶联受体(GPCR)在单体和二聚体之间进行动态平衡。 )),且形成速率恒定。一秒钟之内,GPCR通常会与不同的配偶体经历数个单体和同二聚体形成循环

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