中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Identification of the Conformational transition pathway in PIP2 Opening Kir Channels

文献类型:期刊论文

作者Li JW; Lv SQ(吕守琴); Liu YZ; Pang CL; Chen YF; Zhang SH; Yu H; Long M(龙勉); Zhang HL; Logothetis DE
刊名SCIENTIFIC REPORTS
出版日期2015-06-11
卷号5页码:11289
通讯作者邮箱zhany@hebut.edu.cn ; hailong_an@hebut.edu.cn
ISSN号2045-2322
产权排序[Li, Junwei; Pang, Chunli; Chen, Yafei; Zhang, Suhua; Yu, Hui; Zhan, Yong; An, Hailong] Hebei Univ Technol, Inst Biophys, Sch Sci, Key Lab Mol Biophys, Tianjin 300401, Hebei Province, Peoples R China; [Lu, Shouqin; Long, Mian] Chinese Acad Sci, Inst Mech, Ctr Biomech & Bioengn, Beijing 100190, Peoples R China; [Lu, Shouqin; Long, Mian] Chinese Acad Sci, Inst Mech, Natl Micrograv Lab, Key Lab Micrograv, Beijing 100190, Peoples R China; [Liu, Yuzhi] Shijiazhuang Tiedao Univ, Sch Elect & Elect Engn, Shijiazhuang 050043, Peoples R China; [Zhang, Hailin] Hebei Med Univ, Dept Pharmacol, Key Lab Pharmacol & Toxicol New Drug, Minist Educ,Key Lab Neural & Vasc Biol, Shijiazhuang 050017, Hebei Province, Peoples R China; [Logothetis, Diomedes E.] Virginia Commonwealth Univ, Sch Med, Dept Physiol & Biophys, Richmond, VA 23298 USA
通讯作者An, HL (reprint author), Hebei Univ Technol, Inst Biophys, Sch Sci, Key Lab Mol Biophys, Tianjin 300401, Hebei Province, Peoples R China.
中文摘要The gating of Kir channels depends critically on phosphatidylinositol 4,5-bisphosphate (PIP2), but the detailed mechanism by which PIP2 regulates Kir channels remains obscure. Here, we performed a series of Targeted molecular dynamics simulations on the full-length Kir2.1 channel and, for the first time, were able to achieve the transition from the closed to the open state. Our data show that with the upward motion of the cytoplasmic domain (CTD) the structure of the C-Linker changes from a loop to a helix. The twisting of the C-linker triggers the rotation of the CTD, which induces a small downward movement of the CTD and an upward motion of the slide helix toward the membrane that pulls the inner helix gate open. At the same time, the rotation of the CTD breaks the interaction between the CD- and G-loops thus releasing the G-loop. The G-loop then bounces away from the CD-loop, which leads to the opening of the G-loop gate and the full opening of the pore. We identified a series of interaction networks, between the N-terminus, CD loop, C linker and G loop one by one, which exquisitely regulates the global conformational changes during the opening of Kir channels by PIP2.
分类号一类
类目[WOS]Multidisciplinary Sciences
研究领域[WOS]Science & Technology - Other Topics
收录类别SCI
原文出处http://dx.doi.org/10.1038/srep11289
语种英语
WOS记录号WOS:000356099300001
源URL[http://dspace.imech.ac.cn/handle/311007/54972]  
专题力学研究所_国家微重力实验室
推荐引用方式
GB/T 7714
Li JW,Lv SQ,Liu YZ,et al. Identification of the Conformational transition pathway in PIP2 Opening Kir Channels[J]. SCIENTIFIC REPORTS,2015,5:11289.
APA Li JW.,Lv SQ.,Liu YZ.,Pang CL.,Chen YF.,...&An HL.(2015).Identification of the Conformational transition pathway in PIP2 Opening Kir Channels.SCIENTIFIC REPORTS,5,11289.
MLA Li JW,et al."Identification of the Conformational transition pathway in PIP2 Opening Kir Channels".SCIENTIFIC REPORTS 5(2015):11289.

入库方式: OAI收割

来源:力学研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。