The proposed studies will examine the role of cardiac troponin C (cTnC) in cardiac muscle relaxation.
Specific Aim 1 : Examine factors that control Ca2+ binding and exchange with cTnC in the absence and presence of cTnI by generation of cTnC mutants with dramatically faster or slower Ca2+ dissociation rates from the regulatory site of the cTnC-TnI complex.
Specific Aim 2 : In order to examine the contribution of Ca2+ dissociation from the cTnC-TnI complex to the rate of muscle relaxation, skinned cardiac trabeculae devoid of functional SR will be induced to relax by flash photolysis of a caged Ca2+ chelator diazo-2 after reconstitution with cTnC mutants that exhibit dramatic differences in Ca2+ affinities and dissociation rates.
Specific Aim 3 : In order to examine the contribution of Ca2+ dissociation from the cTnC-TnI complex to the rate of intact cardiac muscle relaxation, contractile properties of electrically stimulated trabeculae will be examined after adenoviral expression of cTnC mutants that exhibit dramatic differences in Ca2+ affinities and dissociation rates. Further insight into the relaxation process will improve understanding of the mechanisms of cardiac muscle diseases that alter relaxation rates.
Davis, Jonathan P; Norman, Catalina; Kobayashi, Tomoyoshi et al. (2007) Effects of thin and thick filament proteins on calcium binding and exchange with cardiac troponin C. Biophys J 92:3195-206 |
Tikunova, Svetlana B; Davis, Jonathan P (2004) Designing calcium-sensitizing mutations in the regulatory domain of cardiac troponin C. J Biol Chem 279:35341-52 |
Davis, Jonathan P; Rall, Jack A; Alionte, Catalina et al. (2004) Mutations of hydrophobic residues in the N-terminal domain of troponin C affect calcium binding and exchange with the troponin C-troponin I96-148 complex and muscle force production. J Biol Chem 279:17348-60 |
Gomes, Aldrin V; Venkatraman, Gayathri; Davis, Jonathan P et al. (2004) Cardiac troponin T isoforms affect the Ca(2+) sensitivity of force development in the presence of slow skeletal troponin I: insights into the role of troponin T isoforms in the fetal heart. J Biol Chem 279:49579-87 |