Studies to localize and characterize the isoform specific functional differences between cardiac and skeletal troponin C
Abstract
Thin filament regulation of muscle contraction is a calcium dependent process mediated by the Tn complex. Calcium is released into the sarcomere and is bound by TnC. The subsequent conformation change in TnC is thought to begin a cascade of events that result in the activation of the actin-myosin ATPase. While the general events of this cascade are known, the molecular mechanisms of this signal transduction event are not. Recombinant DNA techniques, physiological and biochemical studies have been used to localize and characterize the structural domains of TnC that play a role in the calcium dependent signal transduction event that serves to trigger muscle contraction. The strategy exploited the observed functional differences between the isoforms of TnC to map regions of functional significance to the proteins. Chimeric cardiac-skeletal TnC proteins were generated to localize the domains of TnC that are required for maximal function in the myofibrilar ATPase assay. Characterization of these regions has yielded information concerning the molecular mechanism of muscle contraction.
Subject Area
Biochemistry|Molecular biology|Anatomy & physiology|Animals
Recommended Citation
Mullen, James Joseph, "Studies to localize and characterize the isoform specific functional differences between cardiac and skeletal troponin C" (1994). Texas Medical Center Dissertations (via ProQuest). AAI9421930.
https://digitalcommons.library.tmc.edu/dissertations/AAI9421930