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PMID: 2958713 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Location of the ATPase site of myosin determined by three-dimensional electron microscopy.

Nature ·Vol. 329 ·No. 6140 ·1987-00-00 ·Pages 635-8

Tokunaga M, Sutoh K, Toyoshima C, Wakabayashi T

Abstract

Both ATP hydrolysis by myosin and the accompanying cyclic association-dissociation of actin and myosin are essential for muscle contraction. It is important for understanding the molecular mechanism of contraction to know the three-dimensional locations of the two major functional sites of myosin: the ATPase site and the actin-binding site. We have determined the position of the ATPase site of myosin using three-dimensional image reconstruction from electron micrographs and site-specific labelling with the avidin-biotin system. The ATPase site is about 5 nm from the tip of the myosin head and is about 4 nm away from the actin-binding site of myosin. This is the first report of the three-dimensional location of an enzyme active site by electron microscopy.

MeSH Terms
Actins/metabolism Adenosine Diphosphate/metabolism Adenosine Triphosphatases Avidin/metabolism Binding Sites Chemical Phenomena Chemistry, Physical Microscopy, Electron Models, Molecular Models, Structural X-Ray Diffraction
Chemicals
Actins Avidin Adenosine Diphosphate Adenosine Triphosphatases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Tokunaga M
Department of Physics, Faculty of Science, University of Tokyo, Japan.
Sutoh K
Toyoshima C
Wakabayashi T
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1987-00-00
Pages
635-8
Language
English
Region
England
NLM ID
0410462
Subset
IM
Corrections
ErratumIn
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