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KMID : 0360419720080020055
Korean Journal of Pharmacology
1972 Volume.8 No. 2 p.55 ~ p.61
The Role of Ca^(++) on the Superprecipitation of the Contractile Protein



Abstract
Superprecipitation of actomyosin has been considered to be an in vitro model of the muscle contraction.
The superprecipitation and ATPase activity (which supplies the energy for contraction) are influenced by several factors which are the large amount of changes in ionic strength, Mg and ATP concentrations. But those behaviors are found to be promptly influenced by the change in a small range of calcium concentration which can be controlled by the cellular function of muscle physiologically only in the presence of the modullatory proteins, tropomyosin and troponin.
In order to elucidate the precise roles of calcium in the mllscle contraction and relaxation, the effects of calcium on the actin- myosin interaction was observed in the presence of tropomycsin and troponin using the superprecipitation system.
The results are summarized as follows:
1. EGTA (glycol ether diaminetetraacetic acid) prolonged the initiation of the superprecipitation of natural actomyosin.
2. Superprecipitation curve was declined by adding EGTA at the time when the curve reached the half-maximum. The degree of declining was proportional to the amount of EGTA added. Especially, upon adding 0.25 mM EGTA the curve was lowered to the level before the protein superprecipitated. But addition of EGTA did not affect the curve after attaining the maximum.
3. Superprecipitation of Perry myosin B was not affected by EGTA added both before and during the course of the reaction.
4. Tropomyosin did not change the response of Perry myosin B to EGTA added at any time of the reaction.
5. Troponin also did not change the response of Perry myosin B to EGTA.
6. Both tropomyosin and troponin together rendered the Perry myosin B to obtain the same response as natural actomyosin to EGTA.
7. It was concluded that actin-myosin interaction was influenced by the minute change of calcium concentration only in the presence of both tropomyosin and troponin. We could reproduce the contraction and relaxation of the muscle in vitro under the presence of ATP by changing the calcium concentration.
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