Literature DB >> 667108

Studies on the F-actin.tropomyosin.troponin complex. II. Partial reconstitution of thin filament by F-actin, tropomyosin and the tropomyosin binding component of troponin (TN-T).

S Ishiwata, H Kondo.   

Abstract

It was found that thin filaments are reconstituted from F-actin, tropomyosin and the tropomyosin binding component of troponin (TN-T) in vitro according to a self-assembly mechanism. Although a gel structure is formed when the three proteins are mixed in the order F-actin, TN-T and tropomyosin, it is in a metastable state and spontaneously transforms to dispersed filaments in an equilibrium state. The rate of the transformation is largely dependent on temperature. When the mixing order of TN-T and tropomyosin is reversed, large amounts of the complex appear immediately in the dispersed filament form. Dependence on the order of mixing is observed only when the molar ratio of TN-T to tropomyosin is about one, i.e. at the physiological ratio. When the molar ratio of TN-T to tropomyosin is either above or below one, a stable gel form or a stable dispersed filament form, was respectively, obtained independently of the mixing order of the three proteins.

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Year:  1978        PMID: 667108     DOI: 10.1016/0005-2795(78)90017-x

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  3 in total

1.  Tropomyosin modulates pH dependence of isometric tension.

Authors:  H Fujita; S Ishiwata
Journal:  Biophys J       Date:  1999-09       Impact factor: 4.033

Review 2.  Use of thin filament reconstituted muscle fibres to probe the mechanism of force generation.

Authors:  Masataka Kawai; Shin'ichi Ishiwata
Journal:  J Muscle Res Cell Motil       Date:  2006-08-15       Impact factor: 2.698

3.  Structural and functional reconstitution of thin filaments in the contractile apparatus of cardiac muscle.

Authors:  H Fujita; K Yasuda; S Niitsu; T Funatsu; S Ishiwata
Journal:  Biophys J       Date:  1996-11       Impact factor: 4.033

  3 in total

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