Genetically encoded reporters of actin filament organization in living cells and tissues
Carla Silva MartinsiD, François IviD, Shashi Kumar SumaniD, Thomas C. PanagiotouiD, Clara SidoriD, María Ruso-LópeziD, Camille N. PlanckeiD, Shizue OmiiD, Rebecca PagèsiD, Maxime GomesiD, Alex LlewellyniD, Sourish Reddy BandiiD, Laurie RamondiD, Federica ArbizzaniiD, Caio Vaz RimoliiD, Frank SchnorreriD, François RobiniD, Andrew WildeiD, Loïc LeGoffiD, J.D. PédelacqiD, Antoine G. JegouiD, Stéphanie CabantousiD, Sergio A. RincóniD, C. ChandréiD, Sophie BrasseletiD, Manos MavrakisiD
Abstract
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.
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