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,Rebecca Pagès,Maxime Gomes,Sourish Reddy Bandi,Sourish Reddy Bandi,Laurie Ramond,Federica Arbizzani,Caio Vaz Rimoli,Frank Schnorrer,François Robin,Loïc LeGoff,Loïc LeGoff,J.D. Pédelacq
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 precise architectures. Much progress has been made in defining the proteome of the actin cytoskeleton, but a detailed appreciation of the dynamic organizational state of the actin filaments themselves has been hindered by available tools. Fluorescence polarization microscopy is uniquely placed for measuring actin filament organization by exploiting the sensitivity of polarized light excitation to the orientation of fluorophores attached to actin filaments. By engineering fusions of five widely used actin localization reporters to fluorescent proteins with constrained mobility, we have succeeded in developing genetically-encoded, green- and red-fluorescent-protein-based reporters for non-invasive, quantitative measurements of actin filament organization in living cells and tissues by fluorescence polarization microscopy.
科研通智能强力驱动
Strongly Powered by AbleSci AI