Calcium regulates cardiac and skeletal muscle contraction by binding to the thin filament, which contains many copies of actin, tropomyosin, and the three subunits of troponin: TnT, TnI, and Ca2+-binding TnC. Multiple, complex, allosteric interactions among these proteins are responsible for regulating muscle contraction. This project involves measurement of protein-protein interactions within the thin filament, perturbation of these interactions by production of mutant recombinant proteins, and study of their effects on regulation. The experiments will provide insights concerning the conformational states of the thin filament, their relationship to regulation, and their thermodynamic linkage to ligand binding and to thin filament assembly. The long range goal is to understand regulation in terms of transitions in thin filament quaternary structure.
The Aims are (1) Determine the importance of specific regions of tropomyosin for regulation, for thin filament assembly (protein-protein binding) under several distinct conditions, for myosin-actin binding, and for Ca2+ binding. (2) Perform mutagenesis of the inhibitory region of TnI to determine this regions role in the intact thin filament regarding troponin-thin filament binding in the presence or absence of Ca2+ and myosin S1, and for regulation of both myosin ATPase activity and in vitro sliding and force. (3) Obtain structural information regarding troponin within the thin filament, by electron microscopy of thin filaments engineered to have more troponin than normally, and by study of selected actin mutations. (4) Investigate the mechanism of muscle activation s cooperativity, by studying in vitro actin-myosin motility and force using thin filaments with engineered TnC that permits precise control of fractional Ca2+ binding, and also by studying the effects of NH2-terminal truncation of TnT. These four Aims address the process that most directly regulates contraction, and will aid understanding of normal, adaptive, and pathological cardiac and skeletal muscle function.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL038834-12
Application #
2750325
Study Section
Physiology Study Section (PHY)
Project Start
1987-08-01
Project End
2002-07-31
Budget Start
1998-08-01
Budget End
1999-07-31
Support Year
12
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Iowa
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Li, Xiaochuan Edward; Tobacman, Larry S; Mun, Ji Young et al. (2011) Tropomyosin position on F-actin revealed by EM reconstruction and computational chemistry. Biophys J 100:1005-13
Sousa, Duncan; Cammarato, Anthony; Jang, Ken et al. (2010) Electron microscopy and persistence length analysis of semi-rigid smooth muscle tropomyosin strands. Biophys J 99:862-8
Kowlessur, Devanand; Tobacman, Larry S (2010) Troponin regulatory function and dynamics revealed by H/D exchange-mass spectrometry. J Biol Chem 285:2686-94
Kozaili, Julie Mouannes; Leek, Daniel; Tobacman, Larry S (2010) Dual regulatory functions of the thin filament revealed by replacement of the troponin I inhibitory peptide with a linker. J Biol Chem 285:38034-41
Ali, Laith F; Cohen, Joshua M; Tobacman, Larry S (2010) Push and pull of tropomyosin's opposite effects on myosin attachment to actin. A chimeric tropomyosin host-guest study. Biochemistry 49:10873-80
Kowlessur, Devanand; Tobacman, Larry S (2010) Low temperature dynamic mapping reveals unexpected order and disorder in troponin. J Biol Chem 285:38978-86
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