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Myosin Va transport of liposomes in three-dimensional actin networks is modulated by actin filament density, position, and polarity
Author(s) -
Andrew T. Lombardo,
Shane R. Nelson,
Guy G. Kennedy,
Kathleen M. Trybus,
Sam Walcott,
David M. Warshaw
Publication year - 2019
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1901176116
Subject(s) - actin , protein filament , polarity (international relations) , myosin , microfilament , biophysics , liposome , treadmilling , mdia1 , chemistry , microbiology and biotechnology , materials science , cytoskeleton , nanotechnology , biology , biochemistry , cell
Significance Intracellular transport of critical cellular components (e.g. vesicles, organelles, mRNA, chromosomes) is accomplished by myosin Va molecular motors along complicated 3D networks of actin filaments. Disruption of these transport processes leads to debilitating human disease (e.g. Griscelli syndrome), while rearrangement of the 3D actin cytoskeleton is a hallmark of malignant cancers. We found that the various modes of motion (stationary, diffusive-like, or directed) describing how teams of myosin Va transport 350-nm liposome cargos are determined by the 3D position and polarity of the actin filaments within the network that the myosin Va motors interact with. This study demonstrates that the 3D actin filament organization within the network can serve as a potent regulator of myosin Va motor-based intracellular transport.

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