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Updated: Jun 12, 2026

Myosin-Specific Adaptations of In vitro Fluorescence Microscopy-Based Motility Assays
Published on: February 4, 2021
The unconventional regulation of non-muscle myosins
1Jacobs School of Medicine and Biomedical Sciences, Department of Biochemistry, University at Buffalo, Buffalo, NY, USA.
Abstract:
Myosins are actin-based molecular motors that power diverse forms of cellular motility across life. Initially characterized as the contractile machinery of muscle, the superfamily now includes numerous non-muscle classes with distinct cellular functions. Over the past decades, work across numerous actin-based systems has uncovered multiple modes of non-muscle myosin control. Recent advances now expand and, in some cases, challenge conventional regulatory paradigms, underscoring the complexity and adaptability of myosin function in cellular contexts. In this short review, I begin with a concise summary of the major canonical regulatory systems for non-muscle myosins. I follow this by highlighting the major novel regulatory findings from the last decade specifically relating to protein-binding partner activation, structural lipid-binding motifs, co-assembly of mixed classes of myosins, and the regulation of multi-motor complexes by the nanoscale organization of cellular actin. This review will appeal to the general scientific reader aiming to understand the mechanisms regulating myosins outside of the context of muscle and the current state of the non-muscle myosin field.
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Myosin II is a hexamer comprising two heavy chains with globular heads and coiled-coil tails, two regulatory light chains, and two essential light chains. The ATPase sites on the myosin heads hydrolyze ATP, and the released phosphate generates the force for contraction. It is...

