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• W4283165721 abstract "Abstract A transient increase in Ca 2+ concentration in sarcomeres is essential for their proper function. Ca 2+ drives striated muscle contraction via binding to the troponin complex of the thin filament to activate its interaction with the myosin thick filament. In addition to the troponin complex, the myosin essential light chain and myosin‐binding protein C were also found to be Ca 2+ sensitive. However, the effects of Ca 2+ on the function of the tropomodulin family proteins involved in regulating thin filament formation have not yet been studied. Leiomodin, a member of the tropomodulin family, is an actin nucleator and thin filament elongator. Using pyrene‐actin polymerization assay and transmission electron microscopy, we show that the actin nucleation activity of leiomodin is attenuated by Ca 2+ . Using circular dichroism and nuclear magnetic resonance spectroscopy, we demonstrate that the mostly disordered, negatively charged region of leiomodin located between its first two actin‐binding sites binds Ca 2+ . We propose that Ca 2+ binding to leiomodin results in the attenuation of its nucleation activity. Our data provide further evidence regarding the role of Ca 2+ as an ultimate regulator of the ensemble of sarcomeric proteins essential for muscle function. Summary Statement Ca 2+ fluctuations in striated muscle sarcomeres modulate contractile activity via binding to several distinct families of sarcomeric proteins. The effects of Ca 2+ on the activity of leiomodin—an actin nucleator and thin filament length regulator—have remained unknown. In this study, we demonstrate that Ca 2+ binds directly to leiomodin and attenuates its actin nucleating activity. Our data emphasizes the ultimate role of Ca 2+ in the regulation of the sarcomeric protein interactions." @default.
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• W4283165721 date "2022-06-20" @default.
• W4283165721 modified "2023-10-12" @default.
• W4283165721 title "Ca²⁺ attenuates nucleation activity of leiomodin" @default.
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• W4283165721 doi "https://doi.org/10.1002/pro.4358" @default.
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