• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
InsP3R channel gating altered by clustering?InsP3R通道门控会因聚集而改变吗?
Nature. 2011 Oct 12;478(7368):E1-2; discussion E2-3. doi: 10.1038/nature10493.
2
Inositol 1,4,5-trisphosphate receptors in the endoplasmic reticulum: A single-channel point of view.内质网中的肌醇1,4,5-三磷酸受体:单通道视角
Cell Calcium. 2015 Jul;58(1):67-78. doi: 10.1016/j.ceca.2014.12.008. Epub 2014 Dec 18.
3
ER-luminal [Ca] regulation of InsP receptor gating mediated by an ER-luminal peripheral Ca-binding protein.内质网腔[Ca2+]对 InsP 受体门控的调节作用是由内质网腔外周 Ca2+结合蛋白介导的。
Elife. 2020 May 18;9:e53531. doi: 10.7554/eLife.53531.
4
Disease-associated mutations in inositol 1,4,5-trisphosphate receptor subunits impair channel function.疾病相关突变会影响肌醇 1,4,5-三磷酸受体亚基的通道功能。
J Biol Chem. 2020 Dec 25;295(52):18160-18178. doi: 10.1074/jbc.RA120.015683. Epub 2020 Oct 22.
5
Regulation by Ca2+ and inositol 1,4,5-trisphosphate (InsP3) of single recombinant type 3 InsP3 receptor channels. Ca2+ activation uniquely distinguishes types 1 and 3 insp3 receptors.单个重组3型肌醇1,4,5-三磷酸(InsP3)受体通道受Ca2+和肌醇1,4,5-三磷酸(InsP3)的调节。Ca2+激活是1型和3型InsP3受体的独特区别。
J Gen Physiol. 2001 May;117(5):435-46. doi: 10.1085/jgp.117.5.435.
6
Clustering of InsP3 receptors by InsP3 retunes their regulation by InsP3 and Ca2+.肌醇三磷酸(InsP3)使肌醇三磷酸受体聚集,从而重新调整其对肌醇三磷酸和钙离子(Ca2+)的调节。
Nature. 2009 Apr 2;458(7238):655-9. doi: 10.1038/nature07763.
7
Inositol (1,4,5)-trisphosphate (InsP3)-gated Ca channels from cerebellum: conduction properties for divalent cations and regulation by intraluminal calcium.来自小脑的肌醇(1,4,5)-三磷酸(InsP3)门控钙通道:二价阳离子的传导特性及腔内钙的调节
J Gen Physiol. 1994 Nov;104(5):821-56. doi: 10.1085/jgp.104.5.821.
8
Bcl-2 regulation of the inositol 1,4,5-trisphosphate receptor and calcium signaling in normal and malignant lymphocytes: potential new target for cancer treatment.Bcl-2对正常及恶性淋巴细胞中肌醇1,4,5-三磷酸受体和钙信号的调控:癌症治疗的潜在新靶点
Biochim Biophys Acta. 2014 Oct;1843(10):2205-10. doi: 10.1016/j.bbamcr.2014.03.008. Epub 2014 Mar 15.
9
IP3 receptors: Take four IP3 to open.肌醇三磷酸受体:需四个肌醇三磷酸才能打开。
Sci Signal. 2016 Apr 5;9(422):pe1. doi: 10.1126/scisignal.aaf6029.
10
Differential regulation of the InsP₃ receptor type-1 and -2 single channel properties by InsP₃, Ca²⁺ and ATP.三磷酸肌醇受体 1 型和 2 型单通道特性受三磷酸肌醇、钙离子和 ATP 的差异调节。
J Physiol. 2012 Jul 15;590(14):3245-59. doi: 10.1113/jphysiol.2012.228320. Epub 2012 Apr 30.

引用本文的文献

1
Spatial-temporal patterning of Ca signals by the subcellular distribution of IP and IP receptors.通过 IP 和 IP 受体的亚细胞分布对 Ca 信号进行时空模式化。
Semin Cell Dev Biol. 2019 Oct;94:3-10. doi: 10.1016/j.semcdb.2019.01.012. Epub 2019 Feb 2.
2
Inositol 1,4,5-trisphosphate receptors in the endoplasmic reticulum: A single-channel point of view.内质网中的肌醇1,4,5-三磷酸受体:单通道视角
Cell Calcium. 2015 Jul;58(1):67-78. doi: 10.1016/j.ceca.2014.12.008. Epub 2014 Dec 18.
3
Patch-clamp electrophysiology of intracellular Ca2+ channels.细胞内钙离子通道的膜片钳电生理学
Cold Spring Harb Protoc. 2013 Sep 1;2013(9):787-97. doi: 10.1101/pdb.top066217.
4
Permeant calcium ion feed-through regulation of single inositol 1,4,5-trisphosphate receptor channel gating.通透钙离子对单肌醇 1,4,5-三磷酸受体通道门控的调节作用。
J Gen Physiol. 2012 Dec;140(6):697-716. doi: 10.1085/jgp.201210804. Epub 2012 Nov 12.

本文引用的文献

1
Redox-regulated heterogeneous thresholds for ligand recruitment among InsP3R Ca2+-release channels.氧化还原调节的 InsP3R 钙释放通道配体募集的异质阈值。
Biophys J. 2010 Jul 21;99(2):407-16. doi: 10.1016/j.bpj.2010.04.034.
2
Dynamic regulation of IP3 receptor clustering and activity by IP3.肌醇三磷酸(IP3)对IP3受体聚集和活性的动态调节
Channels (Austin). 2009 Jul-Aug;3(4):226-32. doi: 10.4161/chan.3.4.9247. Epub 2009 Jul 12.
3
Clustering of InsP3 receptors by InsP3 retunes their regulation by InsP3 and Ca2+.肌醇三磷酸(InsP3)使肌醇三磷酸受体聚集,从而重新调整其对肌醇三磷酸和钙离子(Ca2+)的调节。
Nature. 2009 Apr 2;458(7238):655-9. doi: 10.1038/nature07763.
4
Graded recruitment and inactivation of single InsP3 receptor Ca2+-release channels: implications for quantal [corrected] Ca2+release.单个肌醇三磷酸受体Ca2+释放通道的分级募集与失活:对量子化[校正后]Ca2+释放的影响
J Physiol. 2006 Jun 15;573(Pt 3):645-62. doi: 10.1113/jphysiol.2006.109504. Epub 2006 Apr 27.
5
Regulation by Ca2+ and inositol 1,4,5-trisphosphate (InsP3) of single recombinant type 3 InsP3 receptor channels. Ca2+ activation uniquely distinguishes types 1 and 3 insp3 receptors.单个重组3型肌醇1,4,5-三磷酸(InsP3)受体通道受Ca2+和肌醇1,4,5-三磷酸(InsP3)的调节。Ca2+激活是1型和3型InsP3受体的独特区别。
J Gen Physiol. 2001 May;117(5):435-46. doi: 10.1085/jgp.117.5.435.
6
Amplitude histograms can identify positively but not negatively coupled channels.幅度直方图可以识别正向耦合通道,但不能识别负向耦合通道。
J Neurosci Methods. 2000 Mar 15;96(2):105-11. doi: 10.1016/s0165-0270(99)00189-2.
7
Single-channel properties in endoplasmic reticulum membrane of recombinant type 3 inositol trisphosphate receptor.重组3型肌醇三磷酸受体内质网膜中的单通道特性
J Gen Physiol. 2000 Mar;115(3):241-56. doi: 10.1085/jgp.115.3.241.
8
Inositol 1,4,5-trisphosphate [correction of tris-phosphate] activation of inositol trisphosphate [correction of tris-phosphate] receptor Ca2+ channel by ligand tuning of Ca2+ inhibition.通过对Ca2+抑制的配体调节实现1,4,5-三磷酸肌醇[纠正为三磷酸]对三磷酸肌醇[纠正为三磷酸]受体Ca2+通道的激活
Proc Natl Acad Sci U S A. 1998 Dec 22;95(26):15821-5. doi: 10.1073/pnas.95.26.15821.
9
Single-channel kinetics, inactivation, and spatial distribution of inositol trisphosphate (IP3) receptors in Xenopus oocyte nucleus.非洲爪蟾卵母细胞核中三磷酸肌醇(IP3)受体的单通道动力学、失活及空间分布
J Gen Physiol. 1997 May;109(5):571-87. doi: 10.1085/jgp.109.5.571.

InsP3R channel gating altered by clustering?

作者信息

Vais Horia, Foskett J Kevin, Mak Don-On Daniel

机构信息

Department of Physiology, University of Pennsylvania Perleman School of Medicine, Philadelphia, Pennsylvania 19104, USA.

出版信息

Nature. 2011 Oct 12;478(7368):E1-2; discussion E2-3. doi: 10.1038/nature10493.

DOI:10.1038/nature10493
PMID:21993761
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3273963/
Abstract
摘要