• 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

一种来源于 KvAP 通道的合成 S6 片段可以自我组装、通透脂双层囊泡,并在双层脂膜中表现出离子通道活性。

A synthetic S6 segment derived from KvAP channel self-assembles, permeabilizes lipid vesicles, and exhibits ion channel activity in bilayer lipid membrane.

机构信息

Molecular and Structural Biology Division, Central Drug Research Institute, Council of Scientific and Industrial Research, Chattar Manzil Palace, Lucknow 226001, India.

出版信息

J Biol Chem. 2011 Jul 15;286(28):24828-41. doi: 10.1074/jbc.M110.209676. Epub 2011 May 18.

DOI:10.1074/jbc.M110.209676
PMID:21592970
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3137058/
Abstract

KvAP is a voltage-gated tetrameric K(+) channel with six transmembrane (S1-S6) segments in each monomer from the archaeon Aeropyrum pernix. The objective of the present investigation was to understand the plausible role of the S6 segment, which has been proposed to form the inner lining of the pore, in the membrane assembly and functional properties of KvAP channel. For this purpose, a 22-residue peptide, corresponding to the S6 transmembrane segment of KvAP (amino acids 218-239), and a scrambled peptide (S6-SCR) with rearrangement of only hydrophobic amino acids but without changing its composition were synthesized and characterized structurally and functionally. Although both peptides bound to the negatively charged phosphatidylcholine/phosphatidylglycerol model membrane with comparable affinity, significant differences were observed between these peptides in their localization, self-assembly, and aggregation properties onto this membrane. S6-SCR also exhibited reduced helical structures in SDS micelles and phosphatidylcholine/phosphatidylglycerol lipid vesicles as compared with the S6 peptide. Furthermore, the S6 peptide showed significant membrane-permeabilizing capability as evidenced by the release of calcein from the calcein-entrapped lipid vesicles, whereas S6-SCR showed much weaker efficacy. Interestingly, although the S6 peptide showed ion channel activity in the bilayer lipid membrane, despite having the same amino acid composition, S6-SCR was significantly inactive. The results demonstrated sequence-specific structural and functional properties of the S6 wild type peptide. The selected S6 segment is probably an important structural element that could play an important role in the membrane interaction, membrane assembly, and functional property of the KvAP channel.

摘要

KvAP 是一种四聚体钾 (K+) 通道,来自古菌 Aeropyrum pernix,每个单体都有六个跨膜 (S1-S6) 片段。本研究的目的是了解 S6 片段的可能作用,该片段被提议形成孔的内 lining,以理解 KvAP 通道的膜组装和功能特性。为此,合成并表征了一个 22 个残基的肽,对应于 KvAP 的 S6 跨膜片段(氨基酸 218-239),以及一个仅重新排列疏水性氨基酸但不改变其组成的 scrambled 肽(S6-SCR)。虽然这两种肽与带负电荷的磷脂酰胆碱/磷脂酰甘油模型膜具有相当的亲和力,但在这些肽在该膜上的定位、自组装和聚集性质方面观察到显著差异。与 S6 肽相比,S6-SCR 在 SDS 胶束和磷脂酰胆碱/磷脂酰甘油脂质体中也表现出减少的螺旋结构。此外,S6 肽表现出显著的膜通透性,如 calcein 从 calcein 包封的脂质体中释放所证明的那样,而 S6-SCR 表现出较弱的功效。有趣的是,尽管 S6 肽在双层脂质膜中表现出离子通道活性,尽管具有相同的氨基酸组成,但 S6-SCR 明显没有活性。结果表明 S6 野生型肽具有序列特异性的结构和功能特性。选定的 S6 片段可能是一个重要的结构元件,它可以在 KvAP 通道的膜相互作用、膜组装和功能特性中发挥重要作用。

相似文献

1
A synthetic S6 segment derived from KvAP channel self-assembles, permeabilizes lipid vesicles, and exhibits ion channel activity in bilayer lipid membrane.一种来源于 KvAP 通道的合成 S6 片段可以自我组装、通透脂双层囊泡,并在双层脂膜中表现出离子通道活性。
J Biol Chem. 2011 Jul 15;286(28):24828-41. doi: 10.1074/jbc.M110.209676. Epub 2011 May 18.
2
A mutation in the S6 segment of the KvAP channel changes the secondary structure and alters ion channel activity in a lipid bilayer membrane.KvAP通道S6片段中的突变会改变二级结构,并改变脂质双分子层膜中的离子通道活性。
Amino Acids. 2022 Nov;54(11):1461-1475. doi: 10.1007/s00726-022-03188-8. Epub 2022 Jul 27.
3
A Shared Mechanism for the Folding of Voltage-Gated K Channels.电压门控钾通道折叠的共享机制。
Biochemistry. 2019 Mar 26;58(12):1660-1671. doi: 10.1021/acs.biochem.9b00068. Epub 2019 Mar 7.
4
Localization of the voltage-sensor toxin receptor on KvAP.电压传感器毒素受体在KvAP上的定位。
Biochemistry. 2004 Aug 10;43(31):10071-9. doi: 10.1021/bi049463y.
5
In vitro folding of KvAP, a voltage-gated K+ channel.KvAP,一种电压门控钾离子通道的体外折叠。
Biochemistry. 2011 Dec 6;50(48):10442-50. doi: 10.1021/bi2012965. Epub 2011 Nov 10.
6
S6 peptide derived from KvAP channel shows cooperativity in gating on bilayer lipid membrane.S6 肽段源自 KvAP 通道,在双层脂膜上表现出门控的协同性。
PLoS One. 2013 Nov 12;8(11):e78845. doi: 10.1371/journal.pone.0078845. eCollection 2013.
7
NMR structural and dynamical investigation of the isolated voltage-sensing domain of the potassium channel KvAP: implications for voltage gating.钾通道 KvAP 隔离电压传感域的 NMR 结构和动力学研究:对电压门控的启示。
J Am Chem Soc. 2010 Apr 28;132(16):5630-7. doi: 10.1021/ja909752r.
8
Conformation and ion-channeling activity of a 27-residue peptide modeled on the single-transmembrane segment of the IsK (minK) protein.基于IsK(minK)蛋白单跨膜片段构建的27个氨基酸残基肽段的构象及离子通道活性
Biochemistry. 1998 Jun 2;37(22):8121-31. doi: 10.1021/bi972112h.
9
Microscopic origin of gating current fluctuations in a potassium channel voltage sensor.钾通道电压传感器门控电流涨落的微观起源。
Biophys J. 2012 Jun 6;102(11):L44-6. doi: 10.1016/j.bpj.2012.04.021. Epub 2012 Jun 5.
10
Profile structures of the voltage-sensor domain and the voltage-gated K(+)-channel vectorially oriented in a single phospholipid bilayer membrane at the solid-vapor and solid-liquid interfaces determined by x-ray interferometry.通过X射线干涉测量法确定在固-气和固-液界面处单个磷脂双分子层膜中矢量取向的电压传感器结构域和电压门控K(+)通道的轮廓结构。
Phys Rev E Stat Nonlin Soft Matter Phys. 2011 Sep;84(3 Pt 1):031911. doi: 10.1103/PhysRevE.84.031911. Epub 2011 Sep 12.

引用本文的文献

1
A mutation in the S6 segment of the KvAP channel changes the secondary structure and alters ion channel activity in a lipid bilayer membrane.KvAP通道S6片段中的突变会改变二级结构,并改变脂质双分子层膜中的离子通道活性。
Amino Acids. 2022 Nov;54(11):1461-1475. doi: 10.1007/s00726-022-03188-8. Epub 2022 Jul 27.
2
S6 peptide derived from KvAP channel shows cooperativity in gating on bilayer lipid membrane.S6 肽段源自 KvAP 通道,在双层脂膜上表现出门控的协同性。
PLoS One. 2013 Nov 12;8(11):e78845. doi: 10.1371/journal.pone.0078845. eCollection 2013.
3
Introduction of a lysine residue promotes aggregation of temporin L in lipopolysaccharides and augmentation of its antiendotoxin property.引入赖氨酸残基可促进抗菌肽天蚕素 L 在脂多糖中的聚集,增强其抗内毒素特性。
Antimicrob Agents Chemother. 2013 Jun;57(6):2457-66. doi: 10.1128/AAC.00169-13. Epub 2013 Mar 11.

本文引用的文献

1
Inducing toxicity by introducing a leucine-zipper-like motif in frog antimicrobial peptide, magainin 2.在蛙抗菌肽 magainin 2 中引入亮氨酸拉链样基序诱导毒性。
Biochem J. 2011 Jun 15;436(3):609-20. doi: 10.1042/BJ20110056.
2
Voltage-dependent gating in a "voltage sensor-less" ion channel.电压门控在一个“无电压传感器”离子通道中的作用。
PLoS Biol. 2010 Feb 23;8(2):e1000315. doi: 10.1371/journal.pbio.1000315.
3
Modulation of KvAP unitary conductance and gating by 1-alkanols and other surface active agents.1-链烷醇和其他表面活性剂对 KvAP 单通道电导和门控的调制。
Biophys J. 2010 Mar 3;98(5):762-72. doi: 10.1016/j.bpj.2009.10.053.
4
Structural and functional changes in a synthetic S5 segment of KvLQT1 channel as a result of a conserved amino acid substitution that occurs in LQT1 syndrome of human.由于人类长QT综合征1型(LQT1)中发生的保守氨基酸取代,KvLQT1通道合成S5片段的结构和功能变化。
Biochim Biophys Acta. 2010 Mar;1798(3):461-70. doi: 10.1016/j.bbamem.2009.12.014. Epub 2010 Jan 4.
5
Design of nontoxic analogues of cathelicidin-derived bovine antimicrobial peptide BMAP-27: the role of leucine as well as phenylalanine zipper sequences in determining its toxicity.源自cathelicidin的牛抗菌肽BMAP-27的无毒类似物设计:亮氨酸以及苯丙氨酸拉链序列在决定其毒性中的作用。
Biochemistry. 2009 Nov 24;48(46):10905-17. doi: 10.1021/bi9009874.
6
Cell selectivity-membrane phospholipids relationship of the antimicrobial effects shown by pleurocidin enantiomeric peptides.杀真菌肽对映体肽抗菌作用的细胞选择性与膜磷脂的关系。
J Pept Sci. 2009 Sep;15(9):601-6. doi: 10.1002/psc.1157.
7
A gating model for the archeal voltage-dependent K(+) channel KvAP in DPhPC and POPE:POPG decane lipid bilayers.二棕榈酰磷脂酰胆碱(DPhPC)和1-棕榈酰-2-油酰磷脂酰乙醇胺:1-棕榈酰-2-油酰磷脂酰甘油(POPE:POPG)癸烷脂质双层中古菌电压依赖性钾离子通道KvAP的门控模型
J Mol Biol. 2009 Jul 31;390(5):902-12. doi: 10.1016/j.jmb.2009.05.062. Epub 2009 May 27.
8
Chloride channels as drug targets.作为药物靶点的氯离子通道
Nat Rev Drug Discov. 2009 Feb;8(2):153-71. doi: 10.1038/nrd2780. Epub 2008 Jan 19.
9
A peptide derived from the putative transmembrane domain in the tail region of E. coli toxin hemolysin E assembles in phospholipid membrane and exhibits lytic activity to human red blood cells: plausible implications in the toxic activity of the protein.一种源自大肠杆菌毒素溶血素E尾部区域假定跨膜结构域的肽在磷脂膜中组装,并对人红细胞表现出裂解活性:这对该蛋白质的毒性活性具有合理的启示。
Biochim Biophys Acta. 2009 Feb;1788(2):538-50. doi: 10.1016/j.bbamem.2008.11.013. Epub 2008 Nov 28.
10
Simultaneous measurements of K+ and calcein release from liposomes and the determination of pore size formed in a membrane.同时测量脂质体中钾离子(K⁺)和钙黄绿素的释放以及测定膜中形成的孔径。
Anal Sci. 2007 May;23(5):517-22. doi: 10.2116/analsci.23.517.