Ca2+ regulation of contraction will be investigated in muscle from the barnacle, Balanus nubilus, from which we have learned much over the past 30 years. In this application to renew a long-lasting, productive grant, the investigators propose to investigate in barnacle muscle fibers 1) how length and cross-bridge attachment modify Ca2+ binding to TnC in these long sarcomere length muscles, 2) whether cross-bridge attachment modifies the off rate of Ca2+ dissociation from TnC measured in fibers, 3) whether this provides a mechanism to couple Ca2+ dissociation and cross-bridge dissociation during relaxation, 4) whether barnacle muscle is dual regulated, 5) changes in TnC structure on activation, and 6) the role of Ca2+ binding to TnC in stabilizing TnC binding to the thin filament and in filament activation. They will use measurements of force in skinned fibers to assess Ca2+ activation, fluorescence of native or recombinant TnC in isolation or exchanged into skinned fibers to measure Ca2+ binding, stopped-flow measurements and activation of caged chelators to assess Ca2+ binding kinetics in isolated TnC or in TnC exchanged into fibers, site-directed mutagenesis of barnacle TnC to test molecular models of regulation, laser confocal microscopy to localize Ca2+ binding in the sarcomere, in vitro motility techniques and extraction of myosin regulatory light chains to test dual regulation. With these results on thin and thick filament regulation and effects of length and cross-bridges on the Ca2+ binding and activation, we will construct a more complete model of activation of contraction. This is important to aid the understanding of Ca2+ regulation of contraction of muscle in general as the mechanisms in other muscles are similar to those in barnacles. In barnacles, the size of individual fibers and sarcomeres allows more parameters to be measured and hypotheses tested. This will provide a more complete understanding of how muscle contraction is regulated, the central step in movement, and how movement itself affects regulation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS008384-30
Application #
6186693
Study Section
Physiology Study Section (PHY)
Program Officer
Lymn, Richard W
Project Start
1978-08-01
Project End
2002-05-31
Budget Start
2000-06-01
Budget End
2002-05-31
Support Year
30
Fiscal Year
2000
Total Cost
$141,071
Indirect Cost
Name
University of Washington
Department
Physiology
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Martyn, D A; Chase, P B (1995) Faster force transient kinetics at submaximal Ca2+ activation of skinned psoas fibers from rabbit. Biophys J 68:235-42
Chase, P B; Martyn, D A; Hannon, J D (1994) Isometric force redevelopment of skinned muscle fibers from rabbit activated with and without Ca2+. Biophys J 67:1994-2001
Chase, P B; Martyn, D A; Hannon, J D (1994) Activation dependence and kinetics of force and stiffness inhibition by aluminiofluoride, a slowly dissociating analogue of inorganic phosphate, in chemically skinned fibres from rabbit psoas muscle. J Muscle Res Cell Motil 15:119-29
Martyn, D A; Chase, P B; Hannon, J D et al. (1994) Unloaded shortening of skinned muscle fibers from rabbit activated with and without Ca2+. Biophys J 67:1984-93
Martyn, D A; Coby, R; Huntsman, L L et al. (1993) Force-calcium relations in skinned twitch and slow-tonic frog muscle fibres have similar sarcomere length dependencies. J Muscle Res Cell Motil 14:65-75
Yates, L D; Coby, R L; Luo, Z et al. (1993) Filament overlap affects TnC extraction from skinned muscle fibres. J Muscle Res Cell Motil 14:392-400
Bond, E F; Gordon, A M (1993) Insulin-induced membrane changes in K(+)-depleted rat skeletal muscle. Am J Physiol 265:C257-65
Gordon, A M; Ridgway, E B (1993) Cross-bridges affect both TnC structure and calcium affinity in muscle fibers. Adv Exp Med Biol 332:183-92;discussion 192-4
Hannon, J D; Chase, P B; Martyn, D A et al. (1993) Calcium-independent activation of skeletal muscle fibers by a modified form of cardiac troponin C. Biophys J 64:1632-7
Allen, T S; Yates, L D; Gordon, A M (1992) Ca(2+)-dependence of structural changes in troponin-C in demembranated fibers of rabbit psoas muscle. Biophys J 61:399-409

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