Literature DB >> 10827989

Different myofilament nearest-neighbor interactions have distinctive effects on contractile behavior.

M V Razumova1, A E Bukatina, K B Campbell.   

Abstract

Cooperativity in contractile behavior of myofilament systems almost assuredly arises because of interactions between neighboring sites. These interactions may be of different kinds. Tropomyosin thin-filament regulatory units may have neighbors in steric blocking positions (off) or steric permissive positions (on). The position of these neighbors influence the tendency for the regulatory unit to assume the on or off state. Likewise, the tendency of a myosin cross-bridge to achieve a force-bearing state may be influenced by whether neighboring cross-bridges are in force-bearing states. Also, a cross-bridge in the force-bearing state may influence the tendency of a regulatory unit to enter the on state. We used a mathematical model to examine the influence of each of these three kinds of neighbor interactions on the steady-state force-pCa relation and on the dynamic force redevelopment process. Each neighbor interaction was unique in its effects on maximal Ca(2+)-activated force, position, and symmetry of the force-pCa curve and on the Hill coefficient. Also, each neighbor interaction had a distinctive effect on the time course of force development as assessed by its rate coefficient, k(dev). These diverse effects suggest that variations in all three kinds of nearest-neighbor interactions may be responsible for a wide variety of currently unexplained observations of myofilament contractile behavior.

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Year:  2000        PMID: 10827989      PMCID: PMC1300894          DOI: 10.1016/S0006-3495(00)76849-4

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  41 in total

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Journal:  J Biol Chem       Date:  1990-11-25       Impact factor: 5.157

2.  Removal of tropomyosin overlap modifies cooperative binding of myosin S-1 to reconstituted thin filaments of rabbit striated muscle.

Authors:  B S Pan; A M Gordon; Z X Luo
Journal:  J Biol Chem       Date:  1989-05-25       Impact factor: 5.157

3.  Hysteresis and the length dependence of calcium sensitivity in chemically skinned rat cardiac muscle.

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Journal:  J Physiol       Date:  1988-07       Impact factor: 5.182

4.  Evidence for a force-dependent component of calcium binding to cardiac troponin C.

Authors:  P A Hofmann; F Fuchs
Journal:  Am J Physiol       Date:  1987-10

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Authors:  B Brenner
Journal:  Proc Natl Acad Sci U S A       Date:  1988-05       Impact factor: 11.205

6.  The thin filament of vertebrate skeletal muscle co-operatively activates as a unit.

Authors:  P W Brandt; M S Diamond; F H Schachat
Journal:  J Mol Biol       Date:  1984-12-05       Impact factor: 5.469

7.  Cooperativity of the calcium switch of regulated rabbit actomyosin system.

Authors:  J M Murray; A Weber
Journal:  Mol Cell Biochem       Date:  1981-02-26       Impact factor: 3.396

8.  Co-operative interactions between troponin-tropomyosin units extend the length of the thin filament in skeletal muscle.

Authors:  P W Brandt; M S Diamond; J S Rutchik; F H Schachat
Journal:  J Mol Biol       Date:  1987-06-20       Impact factor: 5.469

9.  Effect of length and cross-bridge attachment on Ca2+ binding to cardiac troponin C.

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Journal:  Am J Physiol       Date:  1987-07

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Authors:  J M Metzger; R L Moss
Journal:  Science       Date:  1990-03-02       Impact factor: 47.728

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  54 in total

1.  History-dependent mechanical properties of permeabilized rat soleus muscle fibers.

Authors:  Kenneth S Campbell; Richard L Moss
Journal:  Biophys J       Date:  2002-02       Impact factor: 4.033

2.  Nonlinear myofilament regulatory processes affect frequency-dependent muscle fiber stiffness.

Authors:  K B Campbell; M V Razumova; R D Kirkpatrick; B K Slinker
Journal:  Biophys J       Date:  2001-10       Impact factor: 4.033

3.  Cooperative regulation of myosin-actin interactions by a continuous flexible chain I: actin-tropomyosin systems.

Authors:  D A Smith; R Maytum; M A Geeves
Journal:  Biophys J       Date:  2003-05       Impact factor: 4.033

4.  Activation kinetics of skinned cardiac muscle by laser photolysis of nitrophenyl-EGTA.

Authors:  Hunter Martin; Marcus G Bell; Graham C R Ellis-Davies; Robert J Barsotti
Journal:  Biophys J       Date:  2004-02       Impact factor: 4.033

5.  Ising model of cardiac thin filament activation with nearest-neighbor cooperative interactions.

Authors:  John Jeremy Rice; Gustavo Stolovitzky; Yuhai Tu; Pieter P de Tombe
Journal:  Biophys J       Date:  2003-02       Impact factor: 4.033

6.  Coupling of adjacent tropomyosins enhances cross-bridge-mediated cooperative activation in a markov model of the cardiac thin filament.

Authors:  Stuart G Campbell; Fred V Lionetti; Kenneth S Campbell; Andrew D McCulloch
Journal:  Biophys J       Date:  2010-05-19       Impact factor: 4.033

7.  Effects of actin-myosin kinetics on the calcium sensitivity of regulated thin filaments.

Authors:  Nicholas M Sich; Timothy J O'Donnell; Sarah A Coulter; Olivia A John; Michael S Carter; Christine R Cremo; Josh E Baker
Journal:  J Biol Chem       Date:  2010-10-02       Impact factor: 5.157

8.  Approximate model of cooperative activation and crossbridge cycling in cardiac muscle using ordinary differential equations.

Authors:  John Jeremy Rice; Fei Wang; Donald M Bers; Pieter P de Tombe
Journal:  Biophys J       Date:  2008-01-30       Impact factor: 4.033

9.  Interplay between the overlapping ends of tropomyosin and the N terminus of cardiac troponin T affects tropomyosin states on actin.

Authors:  Ranganath Mamidi; John Jeshurun Michael; Mariappan Muthuchamy; Murali Chandra
Journal:  FASEB J       Date:  2013-06-07       Impact factor: 5.191

Review 10.  Myofilament length dependent activation.

Authors:  Pieter P de Tombe; Ryan D Mateja; Kittipong Tachampa; Younss Ait Mou; Gerrie P Farman; Thomas C Irving
Journal:  J Mol Cell Cardiol       Date:  2010-01-04       Impact factor: 5.000

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