Key result
Myosin VI prefers to stay on its current actin filament, whereas myosin Va switches filaments with higher probability at intersections or within bundles.
Myosin VI has a higher propensity to stay on its current actin track compared to myosin Va, a behavior dictated by structural elements other than the lever arm, which may be critical for its role as an intracellular anchor.
Requires cautious extrapolation from animal models; leaves open relevance to human cardiomyocyte trafficking.
Myosin VI (myoVI) and myosin Va (myoVa) serve roles both as intracellular cargo transporters and tethers/anchors. In both capacities, these motors bind to and processively travel along the actin cytoskeleton, a network of intersecting actin filaments and bundles that present directional challenges to these motors. Are myoVI and myoVa inherently different in their abilities to interact and maneuver through the complexities of the actin cytoskeleton? Thus, we created an in vitro model system of intersecting actin filaments and individual unipolar (fascin-actin) or mixed polarity (α-actinin-actin) bundles. The stepping dynamics of individual Qdot-labeled myoVI and myoVa motors were determined on these actin tracks. Interestingly, myoVI prefers to stay on the actin filament it is traveling on, while myoVa switches filaments with higher probability at an intersection or between filaments in a bundle. The structural basis for this maneuverability difference was assessed by expressing a myoVI chimera in which the single myoVI IQ was replaced with the longer, six IQ myoVa lever. The mutant behaved more like myoVI at actin intersections and on bundles, suggesting that a structural element other than the lever arm dictates myoVI's preference to stay on track, which may be critical to its role as an intracellular anchor.
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Ali et al. (2012) studied this question. Myosin VI vs. Myosin Va was evaluated on Stepping dynamics on actin tracks (intersecting filaments and bundles). Myosin VI prefers to stay on its current actin filament, whereas myosin Va switches filaments with higher probability at intersections or within bundles.
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