Oh Dongmyung
Cell Analysis and Modeling, University of Connecticut Health Center, Farmington, CT, 06030, USA.
Mechanobiology Institute, National University of Singapore, Singapore, Singapore.
Methods Mol Biol. 2017;1555:493-511. doi: 10.1007/978-1-4939-6762-9_29.
In the last decade, single molecule tracking (SMT) techniques have emerged as a versatile tool for molecular cell biology research. This approach allows researchers to monitor the real-time behavior of individual molecules in living cells with nanometer and millisecond resolution. As a result, it is possible to visualize biological processes as they occur at a molecular level in real time. Here we describe a method for the real-time visualization of SH2 domain membrane recruitment from the cytoplasm to epidermal growth factor (EGF) induced phosphotyrosine sites on the EGF receptor. Further, we describe methods that utilize SMT data to define SH2 domain membrane dynamics parameters such as binding (τ), dissociation (k ), and diffusion (D) rates. Together these methods may allow us to gain greater understanding of signal transduction dynamics and the molecular basis of disease-related aberrant pathways.
在过去十年中,单分子追踪(SMT)技术已成为分子细胞生物学研究的一种通用工具。这种方法使研究人员能够以纳米和毫秒级分辨率监测活细胞中单个分子的实时行为。因此,能够实时可视化生物过程在分子水平上的发生情况。在这里,我们描述了一种用于实时可视化SH2结构域从细胞质募集到表皮生长因子(EGF)诱导的EGF受体磷酸酪氨酸位点的方法。此外,我们还描述了利用SMT数据来定义SH2结构域膜动力学参数的方法,如结合(τ)、解离(k)和扩散(D)速率。这些方法结合起来可能使我们对信号转导动力学以及疾病相关异常途径的分子基础有更深入的了解。