The Na+-Ca2+ exchanger of cardiac sarcolemma is the dominant Ca2+ efflux mechanism in the myocardium. As such, the Na+-Ca2+ exchanger has a critical role in the regulation of cardiac contractility. Further molecular knowledge of this essential cardiac transporter will help understand both normal and diseased hearts. The long-term goal of this project is to understand the molecular mechanisms involved in the transport process. Towards this goal, the specific aims of the project are as follows: 1. Mutagenesis. This laboratory has recently cloned the cardiac Na+-Ca2+ exchanger. The importance of specific amino acids will now be analyzed by site-directed mutagenesis. Mutants will be expressed in oocytes and analyzed by the giant excised patch technique. 2. Topology. Immunological approaches will be used to determine the arrangement of the Na+-Ca2+ exchange protein in the sarcolemmal membrane. 3. Mapping of binding sites. The Na+-Ca2+ exchanger is capable of binding calmodulin, exchanger inhibitory peptide, regulatory Ca2+, and ankyrin with high affinity. The amino acids involved in the binding of these ligands to the exchanger will be determined by a unique sublibrary approach. 4. Interaction with cytoskeleton. the Na+-Ca2+ exchanger is constrained to specific domains of the sarcolemma by interactions with the cytoskeleton. These interactions of the exchanger with components of the cytoskeleton will be characterized. 5. Protein biochemical approaches. Recombinant exchanger protein will be purified for initial structural studies of the exchanger protein.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL049101-02
Application #
2225198
Study Section
Cardiovascular and Pulmonary Research A Study Section (CVA)
Project Start
1993-04-01
Project End
1998-03-31
Budget Start
1994-04-01
Budget End
1995-03-31
Support Year
2
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Physiology
Type
Schools of Medicine
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
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Besserer, Gabriel Mercado; Nicoll, Debora A; Abramson, Jeff et al. (2012) Characterization and purification of a Na+/Ca2+ exchanger from an archaebacterium. J Biol Chem 287:8652-9
John, Scott A; Ribalet, Bernard; Weiss, James N et al. (2011) Ca2+-dependent structural rearrangements within Na+-Ca2+ exchanger dimers. Proc Natl Acad Sci U S A 108:1699-704
Wang, JuFang; Gao, Erhe; Song, Jianliang et al. (2010) Phospholemman and beta-adrenergic stimulation in the heart. Am J Physiol Heart Circ Physiol 298:H807-15
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Chaptal, Vincent; Ottolia, Michela; Mercado-Besserer, Gabriel et al. (2009) Structure and functional analysis of a Ca2+ sensor mutant of the Na+/Ca2+ exchanger. J Biol Chem 284:14688-92
Ottolia, Michela; Nicoll, Debora A; Philipson, Kenneth D (2009) Roles of two Ca2+-binding domains in regulation of the cardiac Na+-Ca2+ exchanger. J Biol Chem 284:32735-41
Ren, Xiaoyan; Nicoll, Debora A; Galang, Giselle et al. (2008) Intermolecular cross-linking of Na+-Ca2+ exchanger proteins: evidence for dimer formation. Biochemistry 47:6081-7
Xie, Yi; Ottolia, Michela; John, Scott A et al. (2008) Conformational changes of a Ca2+-binding domain of the Na+/Ca2+ exchanger monitored by FRET in transgenic zebrafish heart. Am J Physiol Cell Physiol 295:C388-93
Cavalli, Amy; Eghbali, Mansoureh; Minosyan, Tamara Y et al. (2007) Localization of sarcolemmal proteins to lipid rafts in the myocardium. Cell Calcium 42:313-22

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