Identification of Target Domains of the Cardiac Ryanodine Receptor to Correct Channel Disorder in Failing Hearts
Author(s) -
Takeshi Yamamoto,
Masafumi Yano,
Xiaojuan Xu,
Hitoshi Uchinoumi,
Hiroki Tateishi,
Mamoru Mochizuki,
Tetsuro Oda,
Shigeki Kobayashi,
Noriaki Ikemoto,
Masunori Matsuzaki
Publication year - 2008
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.107.718957
Subject(s) - ryanodine receptor 2 , ryanodine receptor , biophysics , receptor , endoplasmic reticulum , medicine , microbiology and biotechnology , endocrinology , biochemistry , chemistry , biology
We previously demonstrated that defective interdomain interaction between N-terminal (0 to 600) and central regions (2000 to 2500) of ryanodine receptor 2 (RyR2) induces Ca2+ leak in failing hearts and that K201 (JTV519) inhibits the Ca2+ leak by correcting the defective interdomain interaction. In the present report, we identified the K201-binding domain and characterized the role of this novel domain in the regulation of the RyR2 channel.
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