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Mechanical measurements of single actomyosin motor force

Authors :
H, Miyata
H, Yoshikawa
H, Hakozaki
N, Suzuki
T, Furuno
A, Ikegami
K, Kinosita
T, Nishizaka
S, Ishiwata
Source :
Biophysical journal. 68
Publication Year :
1995

Abstract

To elucidate the mechanism of force generation by actomyosin motor, a measuring system was constructed, in which an in vitro motility assay was combined with an optical trapping technique. An actin filament of several micron long was attached to a gelsolin-coated polystyrene bead, and was allowed to interact with a small number (approximately 1/1 micron actin filament) of rabbit skeletal heavy meromyosin (an active subfragment of myosin) molecules bound to a nitrocellulose-coated coverglass. The bead position was determined at 33-ms intervals. We measured the force generation event at relatively low (100-400 nM) ATP concentration so that the occurrence of individual force generation events could be detected with our time resolution. The actin-bound bead held in the optical trap moved in a stepwise manner in the direction of the actin filament only in the presence of ATP. At the trap strength of 0.3 pN/nm, the maximum size of the step was 11 nm, and the maximum force associated with the movement was 3.3 pN.

Details

ISSN :
00063495
Volume :
68
Database :
OpenAIRE
Journal :
Biophysical journal
Accession number :
edsair.pmid..........79673d5159058663f887449a393fe455