• 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

通过截短诱变研究葡萄球菌α-溶血素形成的寡聚膜孔的组装。

Assembly of the oligomeric membrane pore formed by Staphylococcal alpha-hemolysin examined by truncation mutagenesis.

作者信息

Walker B, Krishnasastry M, Zorn L, Bayley H

机构信息

Worcester Foundation for Experimental Biology, Shrewsbury, Massachusetts 01545.

出版信息

J Biol Chem. 1992 Oct 25;267(30):21782-6.

PMID:1400487
Abstract

The alpha-hemolysin (alpha HL) from Staphylococcus aureus causes the lysis of susceptible cells such as rabbit erythrocytes (rRBCs). Lysis is associated with the formation of a hexameric pore in the plasma membrane. Here we show that truncation mutants of alpha HL missing 2 to 22 N-terminal amino acids form oligomers on the surfaces of rRBCs but fail to lyse the cells. By contrast, mutants missing 3 or 5 amino acids at the C terminus are very inefficient at oligomerization but do lyse rRBCs, albeit extremely slowly. The C-terminal truncation mutants, retarded as monomers on the cell surface, undergo a conformational change in which the protease-sensitive loop located near the midpoint of the polypeptide chain becomes occluded. Judged by this criterion, polypeptides truncated at the N terminus, frozen as nonlytic oligomers, are in a similar conformation. A second proteolytic site near the N terminus of the polypeptide becomes inaccessible in the lytic pore formed by the wild-type polypeptide, supporting the idea that a second conformational change occurs upon pore formation. These findings suggest a pathway for assembly of the lytic pore in which alpha HL first binds to target cells as a monomer, which is converted to a nonlytic oligomeric intermediate before formation of the pore. In keeping with this model, an N-terminal truncation mutant blocks the slow lysis induced by a C-terminal truncation mutant, presumably by diverting the weakly lytic subunits into inactive oligomers.

摘要

金黄色葡萄球菌的α-溶血素(αHL)可导致兔红细胞(rRBCs)等敏感细胞发生裂解。细胞裂解与质膜上六聚体孔的形成有关。在此我们表明,缺失2至22个N端氨基酸的αHL截短突变体在rRBCs表面形成寡聚体,但无法裂解细胞。相比之下,在C端缺失3或5个氨基酸的突变体寡聚化效率极低,但确实能裂解rRBCs,尽管速度极其缓慢。C端截短突变体在细胞表面以单体形式滞留,会发生构象变化,位于多肽链中点附近的蛋白酶敏感环会被封闭。以此标准判断,在N端截短的多肽以非裂解性寡聚体形式冻结,处于类似构象。在野生型多肽形成的裂解孔中,多肽N端附近的第二个蛋白水解位点变得无法接近,这支持了在孔形成时发生第二次构象变化的观点。这些发现提示了一种裂解孔组装途径,即αHL首先以单体形式结合到靶细胞上,在孔形成之前转变为非裂解性寡聚中间体。与此模型一致的是,一个N端截短突变体可阻断由一个C端截短突变体诱导的缓慢裂解,大概是通过将弱裂解亚基转移到无活性的寡聚体中实现的。

相似文献

1
Assembly of the oligomeric membrane pore formed by Staphylococcal alpha-hemolysin examined by truncation mutagenesis.通过截短诱变研究葡萄球菌α-溶血素形成的寡聚膜孔的组装。
J Biol Chem. 1992 Oct 25;267(30):21782-6.
2
Functional complementation of staphylococcal alpha-hemolysin fragments. Overlaps, nicks, and gaps in the glycine-rich loop.葡萄球菌α-溶血素片段的功能互补。富含甘氨酸环中的重叠、切口和缺口。
J Biol Chem. 1993 Mar 5;268(7):5285-92.
3
Key residues for membrane binding, oligomerization, and pore forming activity of staphylococcal alpha-hemolysin identified by cysteine scanning mutagenesis and targeted chemical modification.通过半胱氨酸扫描诱变和靶向化学修饰鉴定出的葡萄球菌α-溶血素膜结合、寡聚化和孔形成活性的关键残基。
J Biol Chem. 1995 Sep 29;270(39):23065-71. doi: 10.1074/jbc.270.39.23065.
4
Interactions between residues in staphylococcal alpha-hemolysin revealed by reversion mutagenesis.回复突变分析揭示的葡萄球菌α-溶血素中残基间的相互作用
J Biol Chem. 1995 Sep 29;270(39):23072-6. doi: 10.1074/jbc.270.39.23072.
5
An intermediate in the assembly of a pore-forming protein trapped with a genetically-engineered switch.一种通过基因工程开关捕获的成孔蛋白组装中间体。
Chem Biol. 1995 Feb;2(2):99-105. doi: 10.1016/1074-5521(95)90282-1.
6
Functional expression of the alpha-hemolysin of Staphylococcus aureus in intact Escherichia coli and in cell lysates. Deletion of five C-terminal amino acids selectively impairs hemolytic activity.金黄色葡萄球菌α-溶血素在完整大肠杆菌及细胞裂解物中的功能性表达。C末端五个氨基酸的缺失选择性地损害溶血活性。
J Biol Chem. 1992 May 25;267(15):10902-9.
7
Surface labeling of key residues during assembly of the transmembrane pore formed by staphylococcal alpha-hemolysin.金黄色葡萄球菌α-溶血素形成跨膜孔道组装过程中关键残基的表面标记
FEBS Lett. 1994 Dec 12;356(1):66-71. doi: 10.1016/0014-5793(94)01240-7.
8
The role of the amino terminus in the kinetics and assembly of alpha-hemolysin of Staphylococcus aureus.氨基末端在金黄色葡萄球菌α-溶血素的动力学和组装中的作用。
J Biol Chem. 1997 Oct 3;272(40):24858-63. doi: 10.1074/jbc.272.40.24858.
9
Role of the amino latch of staphylococcal alpha-hemolysin in pore formation: a co-operative interaction between the N terminus and position 217.葡萄球菌α-溶血素的氨基锁在孔形成中的作用:N端与第217位之间的协同相互作用。
J Biol Chem. 2006 Jan 27;281(4):2195-204. doi: 10.1074/jbc.M510841200. Epub 2005 Oct 14.
10
Caveolin-1 binding motif of alpha-hemolysin: its role in stability and pore formation.α-溶血素的小窝蛋白-1结合基序:其在稳定性和孔形成中的作用。
Biochem Biophys Res Commun. 2004 Sep 10;322(1):29-36. doi: 10.1016/j.bbrc.2004.07.073.

引用本文的文献

1
Investigation of Biofilm-Associated Toxin as a Potential Squamous Cell Carcinoma Therapeutic.生物膜相关毒素作为鳞状细胞癌潜在治疗方法的研究。
Microorganisms. 2024 Jan 30;12(2):293. doi: 10.3390/microorganisms12020293.
2
Inhibition of α-hemolysin activity of Staphylococcus aureus by theaflavin 3,3'-digallate.没食子酸棓单宁抑制金黄色葡萄球菌α-溶血素活性。
PLoS One. 2023 Aug 31;18(8):e0290904. doi: 10.1371/journal.pone.0290904. eCollection 2023.
3
Applications and potentials of nanopore sequencing in the (epi)genome and (epi)transcriptome era.
纳米孔测序在(表观)基因组和(表观)转录组时代的应用与潜力
Innovation (Camb). 2021 Aug 11;2(4):100153. doi: 10.1016/j.xinn.2021.100153. eCollection 2021 Nov 28.
4
Redirecting Pore Assembly of Staphylococcal α-Hemolysin by Protein Engineering.通过蛋白质工程重定向葡萄球菌α-溶血素的孔组装
ACS Cent Sci. 2019 Apr 24;5(4):629-639. doi: 10.1021/acscentsci.8b00910. Epub 2019 Mar 25.
5
Infection of Primary Human Alveolar Macrophages Alters Staphylococcus aureus Toxin Production and Activity.原发性人肺泡巨噬细胞感染改变金黄色葡萄球菌毒素的产生和活性。
Infect Immun. 2019 Jun 20;87(7). doi: 10.1128/IAI.00167-19. Print 2019 Jul.
6
P2X-Receptor Antagonists Inhibit the Interaction of S. aureus Hemolysin A with Membranes.P2X 受体拮抗剂抑制金黄色葡萄球菌溶血素 A 与膜的相互作用。
Toxins (Basel). 2017 Oct 19;9(10):332. doi: 10.3390/toxins9100332.
7
A monodisperse transmembrane α-helical peptide barrel.单分散跨膜 α-螺旋肽桶。
Nat Chem. 2017 May;9(5):411-419. doi: 10.1038/nchem.2647. Epub 2016 Nov 14.
8
In vitro directed evolution of alpha-hemolysin by liposome display.通过脂质体展示对α-溶血素进行体外定向进化
Biophysics (Nagoya-shi). 2015 Mar 4;11:67-72. doi: 10.2142/biophysics.11.67. eCollection 2015.
9
Crucial role of perfringolysin O D1 domain in orchestrating structural transitions leading to membrane-perforating pores: a hydrogen-deuterium exchange study.产气荚膜梭菌溶血素O D1结构域在引发导致膜穿孔孔道的结构转变中的关键作用:一项氢-氘交换研究
J Biol Chem. 2014 Oct 10;289(41):28738-52. doi: 10.1074/jbc.M114.577981. Epub 2014 Aug 27.
10
Liposome display for in vitro selection and evolution of membrane proteins.脂质体展示用于体外选择和进化膜蛋白。
Nat Protoc. 2014 Jul;9(7):1578-91. doi: 10.1038/nprot.2014.107. Epub 2014 Jun 5.