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O c t o b e r 1 9 - 2 0 , 2 0 1 8 | T o k y o , J a p a n
Pharma Congress 2018 & Molecular Medicine 2018
& Psychiatric Disorders 2018
Asian Journal of Biomedical and Pharmaceutical Sciences
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ISSN: 2249-622X
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Volume 8
International Conference on
PHARMACEUTICS AND NOVEL DRUG DELIVERY SYSTEMS
19
th
International Conference on
CELLULAR AND MOLECULAR MEDICINE
19
th
Annual Congress on
PSYCHIATRY AND PSYCHIATRIC DISORDERS
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&
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Asian J Biomed Pharmaceut Sci 2018, Volume 8 | DOI: 10.4066/2249-622X-C3-009
NOVEL PROPERTIES OF INDIVIDUAL MYOSIN HEADS IN SKELETAL
MUSCLE AS REVEALED BY EXPERIMENTS USING THE GAS
ENVIRONMENTAL CHAMBER
Haruo Sugi
Teikyo University Medical School, Japan
A
lthough it is generally believed that muscle contraction results from ATP-driven cyclic attachment and detachment between
myosin heads extending from myosin filaments and corresponding myosin-binding sites on actin filaments, the movement
of myosin heads remains to be a matter for debate and speculation. The most straightforward way to visualize and record indi-
vidual myosin head movement coupled with ATP hydrolysis is to use the carbon film-sealed gas environmental chamber (EC),
which enables us to keep biological specimens like muscle actin and myosin filaments in wet, living state in the high vacuum
of a transmission electron microscope. We have succeeded in recording ATP-induced movement of individual myosin heads,
position-marked with gold particles (diameter, 20 nm) via site-directed antibodies to myosin head, and found novel properties
of individual myosin heads, which are summarized as follows: In the absence of ATP, myosin heads take stable neutral position,
around which they fluctuate. In the absence of actin filaments, individual myosin heads move away from, but not towards the
bare region at the center of myosin filaments, i.e. they perform recovery stroke. After exhaustion of applied ATP return to their
neutral position. The above finding indicates that myosin heads can sense the absence or presence of actin filament to determine
their direction of ATP-induced movement, without being guided by actin filaments. In the presence of actin filaments, individual
myosin heads perform power stroke in two different modes depending on experimental conditions. We emphasize that our EC
experiment is the only method to visualize and record ATP-coupled movement of individual myosin heads, while all other meth-
ods can only obtain ambiguous results due to asynchronous nature of myosin head movement.