• 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

成孔蛋白与生物体对环境条件的适应性

Pore-forming proteins and adaptation of living organisms to environmental conditions.

作者信息

Andreeva-Kovalevskaya Zh I, Solonin A S, Sineva E V, Ternovsky V I

机构信息

Skryabin Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences, Pushchino, Moscow Region, 142290, Russia.

出版信息

Biochemistry (Mosc). 2008 Dec;73(13):1473-92. doi: 10.1134/s0006297908130087.

DOI:10.1134/s0006297908130087
PMID:19216713
Abstract

Pore-forming proteins are powerful "tools" for adaptation of living organisms to environmental conditions. A wide range of these proteins isolated from various sources, from viruses to mammals, has been used for the analysis of their role in the processes of intra- and inter-species competition, defense, attack, and signaling. Here we review a large number of pore-forming proteins from the perspective of their functions, structures, and mechanisms of membrane penetration. Various mechanisms of cell damage, executed by these proteins in the course of formation of a pore and after its passing to conducting state, have been considered: endo- and exocytosis, lysis, necrosis, apoptosis, etc. The role of pore-forming proteins in evolution is discussed. The relevance of practical application of pore formers has been shown, including application in nanotechnological constructions.

摘要

成孔蛋白是生物体适应环境条件的强大“工具”。从病毒到哺乳动物等各种来源分离出的多种此类蛋白质,已被用于分析它们在种内和种间竞争、防御、攻击及信号传导过程中的作用。在此,我们从成孔蛋白的功能、结构及膜穿透机制的角度对大量成孔蛋白进行综述。已探讨了这些蛋白质在形成孔道过程中及其转变为传导状态后所执行的各种细胞损伤机制:内吞和外排、裂解、坏死、凋亡等。还讨论了成孔蛋白在进化中的作用。已表明成孔剂实际应用的相关性,包括在纳米技术结构中的应用。

相似文献

1
Pore-forming proteins and adaptation of living organisms to environmental conditions.成孔蛋白与生物体对环境条件的适应性
Biochemistry (Mosc). 2008 Dec;73(13):1473-92. doi: 10.1134/s0006297908130087.
2
Cholesterol-dependent cytolysins.胆固醇依赖性细胞溶素。
Adv Exp Med Biol. 2010;677:56-66. doi: 10.1007/978-1-4419-6327-7_5.
3
Story of Pore-Forming Proteins from Deadly Disease-Causing Agents to Modern Applications with Evolutionary Significance.成孔蛋白的故事:从致命病原体到具有进化意义的现代应用
Mol Biotechnol. 2024 Jun;66(6):1327-1356. doi: 10.1007/s12033-023-00776-1. Epub 2023 Jun 9.
4
Pore formers of the immune system.
Adv Exp Med Biol. 2007;598:325-41. doi: 10.1007/978-0-387-71767-8_23.
5
Pore-forming toxins in Cnidaria.刺胞动物中的孔形成毒素。
Semin Cell Dev Biol. 2017 Dec;72:133-141. doi: 10.1016/j.semcdb.2017.07.026. Epub 2017 Jul 24.
6
Differential Effect of Membrane Composition on the Pore-Forming Ability of Four Different Sea Anemone Actinoporins.膜组成对四种不同海葵孔蛋白成孔能力的差异影响。
Biochemistry. 2016 Dec 6;55(48):6630-6641. doi: 10.1021/acs.biochem.6b01007. Epub 2016 Nov 22.
7
Molecular mechanism of pore formation by actinoporins.肌动蛋白穿孔素形成孔的分子机制。
Toxicon. 2009 Dec 15;54(8):1125-34. doi: 10.1016/j.toxicon.2009.02.026. Epub 2009 Mar 5.
8
Disparate proteins use similar architectures to damage membranes.不同的蛋白质利用相似的结构来破坏细胞膜。
Trends Biochem Sci. 2008 Oct;33(10):482-90. doi: 10.1016/j.tibs.2008.07.004. Epub 2008 Sep 6.
9
Structural determinants for membrane insertion, pore formation and translocation of Clostridium difficile toxin B.艰难梭菌毒素 B 的膜插入、孔形成和易位的结构决定因素。
Mol Microbiol. 2011 Mar;79(6):1643-54. doi: 10.1111/j.1365-2958.2011.07549.x. Epub 2011 Jan 28.
10
Structure of C8alpha-MACPF reveals mechanism of membrane attack in complement immune defense.C8α-MACPF的结构揭示了补体免疫防御中膜攻击的机制。
Science. 2007 Sep 14;317(5844):1552-4. doi: 10.1126/science.1147103.

引用本文的文献

1
Broad-spectrum and powerful neutralization of bacterial toxins by erythroliposomes with the help of macrophage uptake and degradation.通过巨噬细胞摄取和降解,赤藓脂质体对细菌毒素进行广谱且强效的中和作用。
Acta Pharm Sin B. 2022 Nov;12(11):4235-4248. doi: 10.1016/j.apsb.2022.03.015. Epub 2022 Mar 29.
2
Engineered Liposomes Protect Immortalized Immune Cells from Cytolysins Secreted by Group A and Group G Streptococci.工程化脂质体保护永生化免疫细胞免受 A 组和 G 组链球菌分泌的细胞溶解素的侵害。
Cells. 2022 Jan 5;11(1):166. doi: 10.3390/cells11010166.
3
A Monoclonal Antibody against the C-Terminal Domain of Hemolysin II Inhibits HlyII Cytolytic Activity.
一种针对溶血素II C末端结构域的单克隆抗体可抑制HlyII的细胞溶解活性。
Toxins (Basel). 2020 Dec 19;12(12):806. doi: 10.3390/toxins12120806.
4
Genome of the webworm Hyphantria cunea unveils genetic adaptations supporting its rapid invasion and spread.《舞毒蛾基因组揭示了支持其快速入侵和传播的遗传适应性》
BMC Genomics. 2020 Mar 18;21(1):242. doi: 10.1186/s12864-020-6629-6.
5
Piercing Fishes: Porin Expansion and Adaptation to Hematophagy in the Vampire Snail Cumia reticulata.穿孔鱼:吸血蜗牛 Cumia reticulata 中 Porin 的扩张和适应。
Mol Biol Evol. 2018 Nov 1;35(11):2654-2668. doi: 10.1093/molbev/msy156.
6
Cell membrane-derived nanoparticles: emerging clinical opportunities for targeted drug delivery.细胞膜衍生纳米颗粒:靶向药物递送的新兴临床机遇。
Nanomedicine (Lond). 2017 Aug;12(16):2007-2019. doi: 10.2217/nnm-2017-0100. Epub 2017 Jul 26.
7
Comparative genomic analysis reveals genetic features related to the virulence of FORC_013.比较基因组分析揭示了与FORC_013毒力相关的遗传特征。
Gut Pathog. 2017 May 15;9:29. doi: 10.1186/s13099-017-0175-z. eCollection 2017.
8
Role of structural changes induced in biological membranes by hydrolysable tannins from sumac leaves (Rhus typhina L.) in their antihemolytic and antibacterial effects.漆树叶(火炬树)中可水解单宁对生物膜诱导的结构变化在其抗溶血和抗菌作用中的作用。
J Membr Biol. 2014 Jun;247(6):533-40. doi: 10.1007/s00232-014-9664-x. Epub 2014 May 3.
9
Cellular response to Trypanosoma cruzi infection induces secretion of defensin α-1, which damages the flagellum, neutralizes trypanosome motility, and inhibits infection.细胞对克氏锥虫感染的反应会诱导防御素 α-1 的分泌,这种防御素会损害鞭毛,中和锥虫的运动,并抑制感染。
Infect Immun. 2013 Nov;81(11):4139-48. doi: 10.1128/IAI.01459-12. Epub 2013 Aug 26.
10
The pore-forming haemolysins of bacillus cereus: a review.蜡样芽胞杆菌的形成孔溶血素:综述。
Toxins (Basel). 2013 Jun 7;5(6):1119-39. doi: 10.3390/toxins5061119.