• 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

祖先原核离子通道对钙离子选择性的见解。

The insights into calcium ion selectivity provided by ancestral prokaryotic ion channels.

作者信息

Irie Katsumasa

机构信息

Department of Biophysical Chemistry, School of Pharmaceutical Sciences, Wakayama Medical University, Wakayama 640-8156, Japan.

Cellular and Structural Physiology Institute (CeSPI), Nagoya University, Nagoya, Aichi 464-8601, Japan.

出版信息

Biophys Physicobiol. 2021 Nov 19;18:274-283. doi: 10.2142/biophysico.bppb-v18.033. eCollection 2021.

DOI:10.2142/biophysico.bppb-v18.033
PMID:35004101
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8677417/
Abstract

Prokaryotic channels play an important role in the structural biology of ion channels. At the end of the 20 century, the first structure of a prokaryotic ion channel was revealed. Subsequently, the reporting of structures of various prokaryotic ion channels have provided fundamental insights into the structure of ion channels of higher organisms. Voltage-dependent Ca channels (Cavs) are indispensable for coupling action potentials with Ca signaling. Similar to other proteins, Cavs were predicted to have a prokaryotic counterpart; however, it has taken more than 20 years for one to be identified. The homotetrameric channel obtained from generates the calcium ion specific current, so it is named as CavMr. Its selectivity filter contains a smaller number of negatively charged residues than mutant Cavs generated from other prokaryotic channels. CavMr belonged to a different cluster of phylogenetic trees than canonical prokaryotic cation channels. The glycine residue of the CavMr selectivity filter is a determinant for calcium selectivity. This glycine residue is conserved among eukaryotic Cavs, suggesting that there is a universal mechanism for calcium selectivity. A family of homotetrameric channels has also been identified from eukaryotic unicellular algae, and the investigation of these channels can help to understand the mechanism for ion selection that is conserved from prokaryotes to eukaryotes.

摘要

原核生物通道在离子通道的结构生物学中发挥着重要作用。20世纪末,首个原核生物离子通道的结构被揭示。随后,各种原核生物离子通道结构的报道为高等生物离子通道的结构提供了基本见解。电压依赖性钙通道(Cavs)对于将动作电位与钙信号传导偶联至关重要。与其他蛋白质类似,预计Cavs有原核生物对应物;然而,花了20多年才鉴定出一个。从[具体来源未提及]获得的同四聚体通道产生钙离子特异性电流,因此被命名为CavMr。其选择性过滤器中带负电荷的残基数量比从其他原核生物通道产生的突变型Cavs少。与典型的原核生物阳离子通道相比,CavMr属于不同的系统发育树簇。CavMr选择性过滤器的甘氨酸残基是钙选择性的决定因素。该甘氨酸残基在真核生物Cavs中保守,表明存在钙选择性的普遍机制。还从真核单细胞藻类中鉴定出一个同四聚体通道家族,对这些通道的研究有助于理解从原核生物到真核生物保守的离子选择机制。

相似文献

1
The insights into calcium ion selectivity provided by ancestral prokaryotic ion channels.祖先原核离子通道对钙离子选择性的见解。
Biophys Physicobiol. 2021 Nov 19;18:274-283. doi: 10.2142/biophysico.bppb-v18.033. eCollection 2021.
2
A native prokaryotic voltage-dependent calcium channel with a novel selectivity filter sequence.一种具有新型选择性过滤器序列的天然原核电压依赖性钙通道。
Elife. 2020 Feb 25;9:e52828. doi: 10.7554/eLife.52828.
3
Deciphering voltage-gated Na(+) and Ca(2+) channels by studying prokaryotic ancestors.通过研究原核生物祖先来解析电压门控钠通道和钙通道
Trends Biochem Sci. 2015 Sep;40(9):526-34. doi: 10.1016/j.tibs.2015.07.002. Epub 2015 Aug 5.
4
Alternative Mechanisms for Fast Na/Ca Signaling in Eukaryotes via a Novel Class of Single-Domain Voltage-Gated Channels.真核生物中通过新型单域电压门控通道的快速钠/钙信号转导的替代机制。
Curr Biol. 2019 May 6;29(9):1503-1511.e6. doi: 10.1016/j.cub.2019.03.041. Epub 2019 Apr 18.
5
Determining the Crystal Structure of TRPV6确定瞬时受体电位香草酸亚型6(TRPV6)的晶体结构
6
Molecular pore structure of voltage-gated sodium and calcium channels.电压门控钠通道和钙通道的分子孔结构
Braz J Med Biol Res. 1994 Dec;27(12):2781-802.
7
Sodium channel selectivity and conduction: prokaryotes have devised their own molecular strategy.钠离子通道选择性和传导:原核生物设计了自己的分子策略。
J Gen Physiol. 2014 Feb;143(2):157-71. doi: 10.1085/jgp.201311037. Epub 2014 Jan 13.
8
Biophysical Adaptations of Prokaryotic Voltage-Gated Sodium Channels.原核生物电压门控钠离子通道的生物物理适应性。
Curr Top Membr. 2016;78:39-64. doi: 10.1016/bs.ctm.2015.12.003. Epub 2016 Feb 1.
9
A lysine residue from an extracellular turret switches the ion preference in a Cav3 T-Type channel from calcium to sodium ions.一个来自细胞外塔台的赖氨酸残基将 Cav3 T 型钙通道的离子偏好从钙离子切换为钠离子。
J Biol Chem. 2022 Dec;298(12):102621. doi: 10.1016/j.jbc.2022.102621. Epub 2022 Oct 20.
10
Domain-based identification and analysis of glutamate receptor ion channels and their relatives in prokaryotes.基于域的原核生物谷氨酸受体离子通道及其相关蛋白的鉴定与分析。
PLoS One. 2010 Oct 6;5(10):e12827. doi: 10.1371/journal.pone.0012827.

引用本文的文献

1
The structural basis of divalent cation block in a tetrameric prokaryotic sodium channel.四聚体原核钠离子通道中二价阳离子阻断的结构基础。
Nat Commun. 2023 Jul 15;14(1):4236. doi: 10.1038/s41467-023-39987-0.
2
Announcement of BPPB paper awards 2022.2022年BPPB论文奖公告。
Biophys Physicobiol. 2022 Oct 13;19:e190042. doi: 10.2142/biophysico.bppb-v19.0042. eCollection 2022.
3
Editors' Roundup: June 2022.编辑综述:2022年6月。

本文引用的文献

1
Conductance selectivity of Na across the K channel via Na trapped in a tortuous trajectory.Na 通过曲折轨迹捕获的 Na 跨 K 通道的电导选择性。
Proc Natl Acad Sci U S A. 2021 Mar 23;118(12). doi: 10.1073/pnas.2017168118.
2
A Novel Single-Domain Na-Selective Voltage-Gated Channel in Photosynthetic Eukaryotes.光合真核生物中新型的单结构域钠选择性电压门控通道。
Plant Physiol. 2020 Dec;184(4):1674-1683. doi: 10.1104/pp.20.00889. Epub 2020 Oct 1.
3
A native prokaryotic voltage-dependent calcium channel with a novel selectivity filter sequence.
Biophys Rev. 2022 Jun 19;14(3):619-623. doi: 10.1007/s12551-022-00970-6. eCollection 2022 Jun.
一种具有新型选择性过滤器序列的天然原核电压依赖性钙通道。
Elife. 2020 Feb 25;9:e52828. doi: 10.7554/eLife.52828.
4
IP Receptor Plasticity Underlying Diverse Functions.IP 受体可塑性的基础是不同的功能。
Annu Rev Physiol. 2020 Feb 10;82:151-176. doi: 10.1146/annurev-physiol-021119-034433. Epub 2019 Nov 15.
5
High-speed AFM reveals accelerated binding of agitoxin-2 to a K channel by induced fit.高速原子力显微镜揭示了激动毒素-2 通过诱导契合加速与钾通道的结合。
Sci Adv. 2019 Jul 3;5(7):eaax0495. doi: 10.1126/sciadv.aax0495. eCollection 2019 Jul.
6
Alternative Mechanisms for Fast Na/Ca Signaling in Eukaryotes via a Novel Class of Single-Domain Voltage-Gated Channels.真核生物中通过新型单域电压门控通道的快速钠/钙信号转导的替代机制。
Curr Biol. 2019 May 6;29(9):1503-1511.e6. doi: 10.1016/j.cub.2019.03.041. Epub 2019 Apr 18.
7
Structure and mechanism of AMPA receptor - auxiliary protein complexes.AMPA 受体 - 辅助蛋白复合物的结构与机制。
Curr Opin Struct Biol. 2019 Feb;54:104-111. doi: 10.1016/j.sbi.2019.01.011. Epub 2019 Feb 27.
8
Single-particle cryo-EM structure of a voltage-activated potassium channel in lipid nanodiscs.单颗粒冷冻电镜结构解析电压激活钾离子通道在脂质纳米盘中的状态。
Elife. 2018 Aug 15;7:e37558. doi: 10.7554/eLife.37558.
9
Disease-associated missense mutations in GluN2B subunit alter NMDA receptor ligand binding and ion channel properties.谷氨酸受体2B亚基中与疾病相关的错义突变会改变N-甲基-D-天冬氨酸受体的配体结合和离子通道特性。
Nat Commun. 2018 Mar 6;9(1):957. doi: 10.1038/s41467-018-02927-4.
10
Optimized expression and purification of NavAb provide the structural insight into the voltage dependence.优化 NavAb 的表达和纯化,为电压依赖性提供结构见解。
FEBS Lett. 2018 Jan;592(2):274-283. doi: 10.1002/1873-3468.12955. Epub 2018 Jan 9.