双色荧光相互关联光谱(dcFCCS)在纳米尺度上定量相分离。

Yirong Yao, Wenjuan Wang, Chunlai Chen
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引用次数: 1

摘要

液-液相分离(LLPS)导致无膜冷凝物的形成,无膜冷凝物在多种细胞过程中起着重要作用。目前,光学显微镜是观察微米尺度相分离凝聚物最常用的方法。由于光学空间分辨率受到衍射极限(~200 nm)的限制,从单个生物分子到微米尺度凝聚体的动态形成过程仍然是未知的。在此,我们提供了一种详细的方案,应用双色荧光相互关联光谱(dcFCCS)在纳米尺度上检测和量化凝聚体,包括它们的大小、生长速度、分子化学计量以及凝聚体中客户分子的结合亲和力。我们期望定量dcFCCS方法可以广泛应用于研究许多其他重要的相分离体系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Quantifying phase separation at the nanoscale by dual-color fluorescence cross-correlation spectroscopy (dcFCCS).

Quantifying phase separation at the nanoscale by dual-color fluorescence cross-correlation spectroscopy (dcFCCS).

Quantifying phase separation at the nanoscale by dual-color fluorescence cross-correlation spectroscopy (dcFCCS).

Liquid-liquid phase separation (LLPS) causes the formation of membraneless condensates, which play important roles in diverse cellular processes. Currently, optical microscopy is the most commonly used method to visualize micron-scale phase-separated condensates. Because the optical spatial resolution is restricted by the diffraction limit (~200 nm), dynamic formation processes from individual biomolecules to micron-scale condensates are still mostly unknown. Herein, we provide a detailed protocol applying dual-color fluorescence cross-correlation spectroscopy (dcFCCS) to detect and quantify condensates at the nanoscale, including their size, growth rate, molecular stoichiometry, and the binding affinity of client molecules within condensates. We expect that the quantitative dcFCCS method can be widely applied to investigate many other important phase separation systems.

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CiteScore
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