A New Model of Cooperative Myosin-Thin Filament Binding

• Published in: The Journal of biological chemistry 2000-09, Vol.275 (36), p.27587-27593
• Main Authors: Tobacman, L S, Butters, C A
• Format: Article
• Language: English
• Subjects: Actins - chemistry; Actins - metabolism; Animals; Cattle; Kinetics; Models, Biological; Models, Chemical; Models, Molecular; Muscle Fibers, Fast-Twitch - physiology; Muscle, Skeletal - physiology; Myosin Subfragments - chemistry; Myosin Subfragments - metabolism; Myosins - chemistry; Myosins - metabolism; Protein Conformation; Rabbits; Recombinant Proteins - chemistry; Recombinant Proteins - metabolism; Sequence Deletion; Tropomyosin - chemistry; Tropomyosin - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M003648200

Cooperative myosin binding to the thin filament is critical to regulation of cardiac and skeletal muscle contraction. This report delineates and fits to experimental data a new model of this process, in which specific tropomyosin-actin interactions are important, the tropomyosin-tropomyosin polymer is continuous rather than disjointed, and tropomyosin affects myosin-actin binding by shifting among three positions as in recent structural studies. A myosin- and tropomyosin-induced conformational change in actin is proposed, rationalizing the ∼10,000-fold strengthening effect of myosin on tropomyosin-actin binding. Also, myosin S1 binding to regulated filaments containing mutant tropomyosins with internal deletions exhibited exaggerated cooperativity, implying an allosteric effect of tropomyosin on actin and allowing the effect's measurement. Comparisons among the mutants suggest the change in actin is promoted much more strongly by the middle of tropomyosin than by its ends. Regardless of calcium binding to troponin, this change in actin facilitates the shift in tropomyosin position to the actin inner domain, which is required for tight myosin-actin association. It also increases myosin-actin affinity 7-fold compared with the absence of troponin-tropomyosin. Finally, initiation of a shift in tropomyosin position is 100-fold more difficult than is its extension from one actin to the next, producing the myosin binding cooperativity that underlies cooperative activation of muscle contraction.