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Which conformation of the MM-CK molecule is responsible for a strong bond in the M-line of sarcomere?

Physiological research. 2009 ; 58 (3) : 36P.

ISSN 0862-8408
Medvik
Zdroj

Publikační typ
abstrakty MeSH

Abstrakt

Fluorometry of creatine kinase during substrates-induced structural changes of its molecule

Physiological research. 2008 ; 57 (2) : 21P.

ISSN 0862-8408
Medvik
Zdroj

Publikační typ
abstrakty MeSH

Článek online

Creatine kinase binds more firmly to the M-band of rabbit skeletal muscle myofibrils in the presence of its substrates

Molecular and cellular biochemistry. 2007 ; 305 (1-2) : 55-61.

Mol Cell Biochem
ISSN 0300-8177
Medvik
Zdroj

Creatine kinase (CK) (E.C. 2.7.3.2) buffers cellular ATP concentration during fluctuating ATP turnover. Muscle cytosolic CK isoform interacts with various subcellular structures where it is functionally coupled with relevant ATPases. However, how this interaction affects its activity is not known. We have therefore studied the interaction of CK with myofibrils and the role of different conformational states of CK molecule induced by ATP, phosphocreatine, ADP and the ATP-creatine pair. Purified rabbit psoas myofibrils with CK specific activity of 0.4+/-0.02 IU/mg were used. The exchange rates between the myofibrillar M-band and its surroundings were measured with fluorofore conjugated CK (IAF) by the Fluorescence Lost in Photobleaching (FLIP) method within a very narrow pH range 7.1-7.15. For CK-IAF without docked substrates, the time derivative of the initial loss of the fluorescent signal within the M-band equalled -3.26 at the fifth second and the decrease reached 82% by the 67th second. For CK-IAF with added substrates, the derivatives fell into the range of -0.95 to -1.30, with respective decreases from 16 to 46% at the 67th second. The results show that the substrates slowed down the exchange rate. This indicates that the strength of the bond between CK and the M-band of myofibrils increased.