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Cryo-electron microscopy analysis of myosin at work and at rest.
McMillan, Sean N; Scarff, Charlotte A.
Afiliación
  • McMillan SN; The Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds, LS29JT, UK; School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, UK.
  • Scarff CA; The Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds, LS29JT, UK; Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, School of Medicine, Faculty of Medicine & Health, University of Leeds, Leeds, LS29JT, UK. Electronic address: c.a.scarff@leeds.ac.uk.
Curr Opin Struct Biol ; 75: 102391, 2022 08.
Article en En | MEDLINE | ID: mdl-35636003
ABSTRACT
Myosins are a superfamily of ATP-driven actin-dependent molecular motors that are responsible for diverse functions from muscle contraction to cell division. The resolution revolution in cryo-EM has enabled characterisation of the interaction of myosin with its actin track in several states of the myosin motor cycle, for multiple myosin classes, allowing increased insight into the force generation mechanism. A major advancement in our understanding of myosin-2 regulation has come through solving structures of its shutdown state, dysregulation of which is implicated in multiple diseases. This review will discuss what has been accomplished so far with cryoEM, what is still yet to do, but within reach, and how better understanding of myosin structure-function relationships may lead to future therapeutic interventions.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Actinas / Miosinas Idioma: En Revista: Curr Opin Struct Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Actinas / Miosinas Idioma: En Revista: Curr Opin Struct Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article