| Author |
Haraguchi T, Yoshimura K, Inoue Y, Imi T, Hasegawa K, Nagai T, Furusawa H, Mori T, Matsuno K, Ito K.
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| Abstract |
The myosin superfamily encompasses over 70 classes, each with multiple subclasses, and exhibits substantial diversity in properties such as velocity, ATPase activity, duty ratio, and directionality. This functional diversity enables the specialized roles of each myosin in various organisms, organs, and cell types. Beyond these well-characterized parameters, a newly recognized property has recently come into focus: Certain myosins drive actin filaments along chiral curved trajectories. However, this newly identified property remains largely unexplored. Here, we investigated this chiral motion in vitro using Chara corallina myosin XI (CcXI), which drives fast clockwise (CW) movement of actin filaments. This chiral motion arises from asymmetric displacement at the filament's leading tip, and its curvature depends on the myosin density. Surprisingly, at elevated actin concentrations, filaments exhibiting chiral curved motion undergo collective dynamics, spontaneously forming a ring-shaped structure-termed the actin chiral ring (ACR)-that exhibits persistent CW rotation. ACRs display remarkable stability, continuing to rotate at their formation site until ATP is depleted, while maintaining their structure even after rotation ceases. This stability has not been reported among reported collective motions of cytoskeletal proteins driven by various motors. Our findings demonstrate that myosins with chiral activity can autonomously organize actin filaments into stable, chiral structures through collective motion, providing insights into actin self-organization by unconventional myosins. This paradigm offers a mechanistic basis for how motor-driven molecular asymmetry can give rise to coherent structural chirality at the cellular scale-an essential step in the emergence of cell chirality and asymmetry during development.
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