Development of novel arrhythmia therapy using K201 binding core in RyR2 molecle
Development of novel arrhythmia therapy using K201 binding core in RyR2 molecle
批准号:
23591082
负责人:
YAMAMOTO Takeshi
金额:
$3.33万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2011
资助国家:
日本
项目状态:
已结题
起止时间:
2011 至 2013
中文摘要
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英文摘要
We revealed that S2246L mutation site and K201 binding site are making loop and interacting each other. We further analyze the calmodulin binding to RyR2 and find that K201 binding core signal transmitted to calmoulin binding site, and then transmitted to the channel pore. From these data, we find two new target domains for the arrhythmia treatment.
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DOI:
10.1161/circulationaha.111.023259
发表时间:
2011-08-09
期刊:
Circulation
影响因子:
37.8
作者:
[Suetomi T, Yano M, Uchinoumi H, Fukuda M, Hino A, Ono M, Xu X, Tateishi H, Okuda S, Doi M, Kobayashi S, Ikeda Y, Yamamoto T, Ikemoto N, Matsuzaki M]
通讯作者:
Matsuzaki M
CaMKII-mediated Aberrant Ca2+ Release May Play a Key Role in hte Arrhythmogenesis in Cardiac Troponin T-related Familial Hypertrophic Cardiomyopathy
CaMKII 介导的异常 Ca2 释放可能在心肌肌钙蛋白 T 相关家族性肥厚性心肌病的心律失常发生中发挥关键作用
DOI:
--
发表时间:
2012
期刊:
影响因子:
--
作者:
[Tadamitsu Nakashima, Tomoko Ohkusa, Masaaki Yoshida, Masafumi Yano, Shinichi Okuda]
通讯作者:
Shinichi Okuda
カテコラミン誘発性多形性心室頻拍関連遺伝子変異を有する異常なリアノジン受容体において、カルモジュリン結合能改善は催不整脈性を抑制する
提高钙调蛋白结合能力可抑制异常兰尼定受体中儿茶酚胺诱导的多态性室性心动过速相关基因突变的致心律失常
DOI:
--
发表时间:
2013
期刊:
影响因子:
--
作者:
[Shigeta T, Aoyama M, Bando YK, Monji A, Mitsui T, Takatsu M, et al., 福田昌和,山本 健,加藤孝佳,村上和華子,立石裕樹,土居正浩,奥田真一,小林茂樹,矢野雅文]
通讯作者:
福田昌和,山本 健,加藤孝佳,村上和華子,立石裕樹,土居正浩,奥田真一,小林茂樹,矢野雅文
Fixing Ca^<2+> Leakage From Cardiac Ryanodine Receptor by Low-dose ofβBlocker Safely Enhances Inotropic Response to Milrinone in Acute Heart Failure
通过低剂量β受体阻滞剂修复心脏兰尼丁受体的 Ca^<2+> 渗漏可安全增强急性心力衰竭患者对米力农的正性肌力反应
DOI:
--
发表时间:
2012
期刊:
影响因子:
--
作者:
[Shigeki Kobayashi, Wakako Murakami, Takayoshi Kato, Masakazu Fukuda, Akihiro Hino, Hiroki Tateishi, Takeshi Yamamoto, Takeshi Yamamoto, Masafumi Yano, Masunori Matsuzaki]
通讯作者:
Masunori Matsuzaki
Mutation-Linked Defective Interdomain Interactions Within Ryanodine Receptor Cause Aberrant Ca2+ Release Leading to Catecholaminergic Polymorphic Ventricular Tachycardia
兰尼碱受体内突变相关的缺陷性域间相互作用导致异常 Ca2 释放,导致儿茶酚胺能多形性室性心动过速
DOI:
--
发表时间:
2011-08
期刊:
Circulation
影响因子:
37.8
作者:
[Xu X., Tateishi H., Okuda S., Doi M., Kobayashi S., Ikeda Y., Yamamoto T., Ikemoto N., Matsuzaki M.]
通讯作者:
Matsuzaki M.
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