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PMID: 11133243 Published · ppublish English Journal Article

In vitro assays of processive myosin motors.

Methods (San Diego, Calif.) ·Vol. 22 ·No. 4 ·2000-12-00 ·Pages 373-81

Rock RS, Rief M, Mehta AD, Spudich JA

Abstract

Myosin V is an actin-based motor thought to be involved in vesicle transport. Since the properties of such a motor may be expected to differ from those of muscle myosin II, we have examined myosin V-driven movement using a combination of gliding filament and optical trap assays to observe single molecules with high resolution. The results clearly demonstrate that brain myosin V is a highly efficient processive motor. In vitro motility assays at low myosin V densities reveal apparent single-molecule supported movement. Processive stepping was also observed in optical trapping assays of myosin V-driven motion. Here the methods that were used to demonstrate the processivity of myosin V are described. These methods include density-dependent assays that eliminate the possibility of aggregation or chance colocalization of multiple motors being responsible for apparent single-molecule motility. Such assays will be useful tools for identifying other processive classes of myosins.

MeSH Terms
Actin Cytoskeleton/physiology Biophysics/methods Calmodulin-Binding Proteins/physiology Molecular Motor Proteins/physiology Movement/physiology Myosin Light Chains/physiology Myosin Type V Nerve Tissue Proteins/physiology Optics and Photonics
Chemicals
Calmodulin-Binding Proteins Molecular Motor Proteins Myosin Light Chains Nerve Tissue Proteins chicken brain myosin-V p190 Myosin Type V
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Rock R S
Department of Biochemistry, Stanford University School of Medicine, Beckman Center B405, Stanford, California 94305-5307, USA.
Rief M
Mehta A D
Spudich J A
Article Info
Journal
Methods (San Diego, Calif.)
Abbr.
Methods
ISSN
1046-2023
Published
2000-12-00
Pages
373-81
Language
English
Region
United States
NLM ID
9426302
Subset
IM
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