蛋白质丝
细胞生物学
肌动蛋白
基因工程
转基因生物
生物
遗传学
基因
作者
Carla Silva Martins,François Iv,Shashi Kumar Suman,Thomas C. Panagiotou,Clara Sidor,María Ruso-López,Camille N. Plancke,Shizue Omi,Maxime Gomes,Alex Llewellyn,Sourish Reddy Bandi,Laurie Ramond,Federica Arbizzani,Caio Vaz Rimoli,Frank Schnorrer,François Robin,Andrew Wilde,Loïc LeGoff,J.D. Pédelacq,Stéphanie Cabantous
标识
DOI:10.1101/2024.04.26.591305
摘要
SUMMARY The cytoskeletal protein actin is crucial for cell shape and integrity throughout eukaryotes. Actin filaments perform essential biological functions, including muscle contraction, cell division and tissue morphogenesis. These diverse activities are achieved through the ability of actin filaments to be arranged into diverse architectures, but a detailed appreciation of the dynamic organizational state of the actin filaments has been hindered by available tools. Fluorescence polarization microscopy is uniquely placed for measuring actin organization by exploiting the sensitivity of polarized light excitation to the orientation of fluorophores attached to actin filaments. By engineering constrained fluorescent protein fusions to widely used actin localization reporters, we have succeeded in developing novel genetically-encoded reporters for non-invasive, quantitative measurements of actin filament organization in living cells by fluorescence polarization microscopy. We show examples of actin organization measurements in living mammalian cells in culture, as well as in vivo in fission yeast, C. elegans and Drosophila .
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