Source:http://linkedlifedata.com/resource/pubmed/id/15591045
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2005-2-14
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pubmed:abstractText |
The ryanodine receptor-calcium release channel complex (RyR) plays a pivotal role in excitation-contraction coupling in skeletal and cardiac muscle. RyR channel activity is modulated by interaction with FK506-binding protein (FKBP), and disruption of the RyR-FKBP association has been implicated in cardiomyopathy, cardiac hypertrophy, and heart failure. Evidence for an interaction between RyR and FKBP is well documented, both in skeletal muscle (RyR1-FKBP12) and in cardiac muscle (RyR2-FKBP12.6), however definition of the FKBP-binding site remains elusive. Early reports proposed interaction of a short RyR central domain with FKBP12/12.6, however this site has been questioned, and recently an alternative FKBP12.6 interaction site has been identified within the N-terminal half of RyR2. In this study, we report evidence for the human RyR2 C-terminal domain as a novel FKBP12.6-binding site. Using competition binding assays, we find that short C-terminal RyR2 fragments can displace bound FKBP12.6 from the native RyR2, although they are unable to exclusively support interaction with FKBP12.6. However, expression of a large RyR2 C-terminal construct in mammalian cells encompassing the pore-forming transmembrane domains exhibits rapamycin-sensitive binding specifically to FKBP12.6 but not to FKBP12. We also obtained some evidence for involvement of the RyR2 N-terminal, but not the central domain, in FKBP12.6 interaction. Our studies suggest that a novel interaction site for FKBP12.6 may be present at the RyR2 C terminus, proximal to the channel pore, a sterically appropriate location that would enable this protein to play a central role in the modulation of this critical ion channel.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Ryanodine Receptor Calcium Release...,
http://linkedlifedata.com/resource/pubmed/chemical/Tacrolimus Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/tacrolimus binding protein 1B
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
18
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pubmed:volume |
280
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5475-85
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15591045-Amino Acid Sequence,
pubmed-meshheading:15591045-Animals,
pubmed-meshheading:15591045-Binding, Competitive,
pubmed-meshheading:15591045-Cell Line,
pubmed-meshheading:15591045-Humans,
pubmed-meshheading:15591045-Immunoprecipitation,
pubmed-meshheading:15591045-Molecular Sequence Data,
pubmed-meshheading:15591045-Myocardium,
pubmed-meshheading:15591045-Peptide Fragments,
pubmed-meshheading:15591045-Protein Binding,
pubmed-meshheading:15591045-Protein Structure, Tertiary,
pubmed-meshheading:15591045-Ryanodine Receptor Calcium Release Channel,
pubmed-meshheading:15591045-Swine,
pubmed-meshheading:15591045-Tacrolimus Binding Proteins
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pubmed:year |
2005
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pubmed:articleTitle |
Interaction of FKBP12.6 with the cardiac ryanodine receptor C-terminal domain.
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pubmed:affiliation |
Wales Heart Research Institute, Department of Cardiology, University of Wales College of Medicine, Cardiff CF14 4XN, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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