Abstract

This grant examines the participation of the DHPR beta1a subunit in excitation-contraction coupling in skeletal muscle. The central hypothesis is that protein-protein interactions between the DHPR beta1a subunit and RyR1 are essential for signals transmitted from the DHPR to the RyR1 channel during EC coupling. The hypothesis is tested by a combination of in-vitro recombinant protein and cell-based approaches. Proximity determinations using FRET are used to investigate a structural model proposed for beta1a. Recombinant protein and in-vitro expression approaches are used to map domains and molecular motifs in beta1a and RyR1 that bind to each other. Electrophysiological approaches implemented in primary cultured myotubes from beta1 KO and RyR1 KO mice investigate the functional consequences of the interaction of beta1a and RyR1.
Aim 1 will develop a model of the domain organization of beta1a based on its homology to the MAGUK protein PSD-95. We propose to investigate the domain organization of beta1a using FRET in beta1a variants with fused CFP as the donor and covalently-bound FIAsH as the acceptor.
Aim 2 will examine the role of the C-terminal domain of beta1a in EC coupling. Cell-based mutagenesis and in-vitro pull-down strategies are used to assess the functional significance of C- and N-terminal heptad repeats present in beta1a.
Aim 3 will characterize a critical region of RyR1 that binds beta1a and determine functional correlates of the beta1a-RyR1 interaction. Cell-based mutagenesis and in-vitro pull-down strategies will determine the significance of a putative binding site for beta1a located in the 3490-3523 region of RyR1. A beta1a/RyR1 could bring about strong docking of the DHPR and RyR1, and/or could be essential to the generation of the signal that opens RyR1. These two functions, although seemingly dissimilar, may represent two manifestations of the same molecular interaction. The purpose of this application is to gain a detailed molecular insight on how DHPR beta1a interacts with RyR1, and to pursue the functional consequences of this interaction. This information is crucial for understanding the molecular basis of normal EC coupling as well as the molecular basis of diseased states in which EC coupling is drastically altered.

  Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR046448-07
Application #
7007350
Study Section
Skeletal Muscle and Exercise Physiology Study Section (SMEP)
Program Officer
Boyce, Amanda T
Project Start
2000-02-16
Project End
2007-11-30
Budget Start
2005-12-01
Budget End
2007-11-30
Support Year
7
Fiscal Year
2006
Total Cost
$343,178
Indirect Cost

  Institution

Name
University of Wisconsin Madison
Department
Physiology
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715

  Publications

Bhattacharya, Dipankar; Mehle, Andrew; Kamp, Timothy J et al. (2015) Intramolecular ex vivo Fluorescence Resonance Energy Transfer (FRET) of Dihydropyridine Receptor (DHPR) ?1a Subunit Reveals Conformational Change Induced by RYR1 in Mouse Skeletal Myotubes. PLoS One 10:e0131399
Balijepalli, Ravi C; Delisle, Brian P; Balijepalli, Sadguna Y et al. (2007) Kv11.1 (ERG1) K+ channels localize in cholesterol and sphingolipid enriched membranes and are modulated by membrane cholesterol. Channels (Austin) 1:263-72
Carbonneau, Leah; Bhattacharya, Dipankar; Sheridan, David C et al. (2005) Multiple loops of the dihydropyridine receptor pore subunit are required for full-scale excitation-contraction coupling in skeletal muscle. Biophys J 89:243-55
Cheng, Weijun; Altafaj, Xavier; Ronjat, Michel et al. (2005) Interaction between the dihydropyridine receptor Ca2+ channel beta-subunit and ryanodine receptor type 1 strengthens excitation-contraction coupling. Proc Natl Acad Sci U S A 102:19225-30
Coronado, Roberto; Ahern, Chris A; Sheridan, David C et al. (2004) Functional equivalence of dihydropyridine receptor alpha1S and beta1a subunits in triggering excitation-contraction coupling in skeletal muscle. Biol Res 37:565-75
Pouvreau, Sandrine; Berthier, Christine; Blaineau, Sylvie et al. (2004) Membrane cholesterol modulates dihydropyridine receptor function in mice fetal skeletal muscle cells. J Physiol 555:365-81
Sheridan, David C; Cheng, Weijun; Carbonneau, Leah et al. (2004) Involvement of a heptad repeat in the carboxyl terminus of the dihydropyridine receptor beta1a subunit in the mechanism of excitation-contraction coupling in skeletal muscle. Biophys J 87:929-42
Sheridan, David C; Carbonneau, Leah; Ahern, Chris A et al. (2003) Ca2+-dependent excitation-contraction coupling triggered by the heterologous cardiac/brain DHPR beta2a-subunit in skeletal myotubes. Biophys J 85:3739-57
Sheridan, David C; Cheng, Weijun; Ahern, Chris A et al. (2003) Truncation of the carboxyl terminus of the dihydropyridine receptor beta1a subunit promotes Ca2+ dependent excitation-contraction coupling in skeletal myotubes. Biophys J 84:220-37
Ahern, Chris A; Sheridan, David C; Cheng, Weijun et al. (2003) Ca2+ current and charge movements in skeletal myotubes promoted by the beta-subunit of the dihydropyridine receptor in the absence of ryanodine receptor type 1. Biophys J 84:942-59

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