Hazawa Masaharu, Amemori Shogo, Nishiyama Yoshio, Iga Yoshihiro, Iwashima Yuki, Kobayashi Akiko, Nagatani Hirohisa, Mizuno Motohiro, Takahashi Kenji, Wong Richard W
Institute for Frontier Science Initiative, Kanazawa University, Kanazawa, Ishikawa, Japan.
Institute of Science and Engineering, Kanazawa University, Kanazawa, Ishikawa, Japan.
iScience. 2021 Jul 15;24(8):102865. doi: 10.1016/j.isci.2021.102865. eCollection 2021 Aug 20.
Biomolecules may undergo liquid-liquid phase separation (LLPS) to spatiotemporally compartmentalize and regulate diverse biological processes. Because the number of tools to directly probe LLPS is limited (ie. FRAP, FRET, fluorescence microscopy, fluorescence anisotropy, circular dichroism, etc.), the physicochemical traits of phase-separated condensates remain largely elusive. Here, we introduce a light-switching dipyrene probe (Pyr-A) that forms monomers in either hydrophobic or viscous environments, and intramolecular excimers in aqueous solutions. By exploiting their distinct fluorescence emission spectra, we used fluorescent microscopic imaging to study phase-separated condensates formed by protein droplets and membraneless intracellular organelles (centrosomes). Ratiometric measurement of excimer and monomer fluorescence intensities showed that protein droplets became hydrophobic and viscous as their size increased. Moreover, centrosomes became hydrophobic and viscous during maturation. Our results show that Pyr-A is a valuable tool to characterize LLPS and enhance our understanding of phase separation underlying biological functions.
生物分子可能会经历液-液相分离(LLPS),从而在时空上进行区室化并调节多种生物过程。由于直接探测LLPS的工具数量有限(例如,荧光漂白恢复技术、荧光共振能量转移、荧光显微镜、荧光偏振、圆二色性等),相分离凝聚物的物理化学特性在很大程度上仍然难以捉摸。在此,我们引入了一种光开关二芘探针(Pyr-A),它在疏水或粘性环境中形成单体,在水溶液中形成分子内激基缔合物。通过利用它们不同的荧光发射光谱,我们使用荧光显微镜成像来研究由蛋白质液滴和无膜细胞器(中心体)形成的相分离凝聚物。激基缔合物和单体荧光强度的比率测量表明,蛋白质液滴随着尺寸的增加而变得疏水且粘稠。此外,中心体在成熟过程中变得疏水且粘稠。我们的结果表明,Pyr-A是表征LLPS并增强我们对生物功能背后相分离理解的有价值工具。