• 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
Predicting inter-species cross-talk in two-component signalling systems.预测双组份信号系统中的种间串扰。
PLoS One. 2012;7(5):e37737. doi: 10.1371/journal.pone.0037737. Epub 2012 May 22.
2
Agents of change - concepts in Mycobacterium tuberculosis Ser/Thr/Tyr phosphosignalling.变化因子——结核分枝杆菌丝氨酸/苏氨酸/酪氨酸磷酸信号传导中的概念
Mol Microbiol. 2014 Oct;94(2):231-41. doi: 10.1111/mmi.12747. Epub 2014 Aug 25.
3
Two-component signal transduction pathways regulating growth and cell cycle progression in a bacterium: a system-level analysis.调节细菌生长和细胞周期进程的双组分信号转导途径:系统水平分析
PLoS Biol. 2005 Oct;3(10):e334. doi: 10.1371/journal.pbio.0030334. Epub 2005 Sep 27.
4
Engineering key components in a synthetic eukaryotic signal transduction pathway.构建合成真核信号转导通路中的关键组件。
Mol Syst Biol. 2009;5:270. doi: 10.1038/msb.2009.28. Epub 2009 May 19.
5
Kinetic buffering of cross talk between bacterial two-component sensors.细菌双组分传感器之间串扰的动力学缓冲
J Mol Biol. 2009 Jul 17;390(3):380-93. doi: 10.1016/j.jmb.2009.05.007. Epub 2009 May 13.
6
The two-component signalling networks of Mycobacterium tuberculosis display extensive cross-talk in vitro.结核分枝杆菌的双组分信号网络在体外表现出广泛的相互作用。
Biochem J. 2015 Jul 1;469(1):121-34. doi: 10.1042/BJ20150268. Epub 2015 May 1.
7
Receptor domains of two-component signal transduction systems.双组分信号转导系统的受体结构域。
Mol Biosyst. 2011 May;7(5):1388-98. doi: 10.1039/c0mb00329h. Epub 2011 Feb 24.
8
Unlimited multistability and Boolean logic in microbial signalling.微生物信号传导中的无限多稳态性与布尔逻辑
J R Soc Interface. 2015 Jul 6;12(108):20150234. doi: 10.1098/rsif.2015.0234.
9
Computational modelling of the BRI1 receptor system.BRI1 受体系统的计算建模。
Plant Cell Environ. 2013 Sep;36(9):1728-37. doi: 10.1111/pce.12077. Epub 2013 Mar 12.
10
Cross-talk suppression between the CpxA-CpxR and EnvZ-OmpR two-component systems in E. coli.大肠杆菌中CpxA-CpxR和EnvZ-OmpR双组分系统之间的串扰抑制
Mol Microbiol. 2008 Oct;70(2):494-506. doi: 10.1111/j.1365-2958.2008.06426.x. Epub 2008 Aug 29.

引用本文的文献

1
Regulation of the AbrA1/A2 two-component system in Streptomyces coelicolor and the potential of its deletion strain as a heterologous host for antibiotic production.天蓝色链霉菌中AbrA1/A2双组分系统的调控及其缺失菌株作为抗生素生产异源宿主的潜力。
PLoS One. 2014 Oct 10;9(10):e109844. doi: 10.1371/journal.pone.0109844. eCollection 2014.
2
Co-culture systems and technologies: taking synthetic biology to the next level.共培养系统和技术:将合成生物学提升到新的水平。
J R Soc Interface. 2014 Jul 6;11(96). doi: 10.1098/rsif.2014.0065.

本文引用的文献

1
Genome sequence of Rhodobacter sphaeroides Strain WS8N.Rhodobacter sphaeroides Strain WS8N 基因组序列。
J Bacteriol. 2011 Aug;193(15):4027-8. doi: 10.1128/JB.05257-11. Epub 2011 May 27.
2
Regulation of cross-talk in yeast MAPK signaling pathways.酵母 MAPK 信号通路交互调控。
Curr Opin Microbiol. 2010 Dec;13(6):677-83. doi: 10.1016/j.mib.2010.09.001. Epub 2010 Sep 27.
3
Specificity of localization and phosphotransfer in the CheA proteins of Rhodobacter sphaeroides.Rhodobacter sphaeroides CheA 蛋白的定位和磷酸转移特异性。
Mol Microbiol. 2010 Apr;76(2):318-30. doi: 10.1111/j.1365-2958.2010.07095.x.
4
Designing customized cell signalling circuits.设计定制的细胞信号通路。
Nat Rev Mol Cell Biol. 2010 Jun;11(6):393-403. doi: 10.1038/nrm2904. Epub 2010 May 19.
5
Rewiring cells: synthetic biology as a tool to interrogate the organizational principles of living systems.重塑细胞:合成生物学作为一种探究生命系统组织原则的工具。
Annu Rev Biophys. 2010;39:515-37. doi: 10.1146/annurev.biophys.050708.133652.
6
Interaction fidelity in two-component signaling.二组分信号转导中的相互作用保真度。
Curr Opin Microbiol. 2010 Apr;13(2):190-7. doi: 10.1016/j.mib.2010.01.007. Epub 2010 Feb 3.
7
Evolution and phyletic distribution of two-component signal transduction systems.二组分信号转导系统的进化和系统发生分布。
Curr Opin Microbiol. 2010 Apr;13(2):219-25. doi: 10.1016/j.mib.2009.12.011. Epub 2010 Feb 3.
8
Deciphering chemotaxis pathways using cross species comparisons.利用跨物种比较解析趋化性通路。
BMC Syst Biol. 2010 Jan 11;4:3. doi: 10.1186/1752-0509-4-3.
9
The Pfam protein families database.Pfam 蛋白质家族数据库。
Nucleic Acids Res. 2010 Jan;38(Database issue):D211-22. doi: 10.1093/nar/gkp985. Epub 2009 Nov 17.
10
The MiST2 database: a comprehensive genomics resource on microbial signal transduction.MiST2 数据库:微生物信号转导的综合基因组学资源。
Nucleic Acids Res. 2010 Jan;38(Database issue):D401-7. doi: 10.1093/nar/gkp940. Epub 2009 Nov 9.

预测双组份信号系统中的种间串扰。

Predicting inter-species cross-talk in two-component signalling systems.

机构信息

Department of Biochemistry, Oxford Centre for Integrative Systems Biology, University of Oxford, Oxford, United Kingdom.

出版信息

PLoS One. 2012;7(5):e37737. doi: 10.1371/journal.pone.0037737. Epub 2012 May 22.

DOI:10.1371/journal.pone.0037737
PMID:22629451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3358273/
Abstract

Phosphosignalling pathways are an attractive option for the synthetic biologist looking for a wide repertoire of modular components from which to build. We demonstrate that two-component systems can be used in synthetic biology. However, their potential is limited by the fact that host cells contain many of their own phosphosignalling pathways and these may interact with, and cross-talk to, the introduced synthetic components. In this paper we also demonstrate a simple bioinformatic tool that can help predict whether interspecies cross-talk between introduced and native two-component signalling pathways will occur and show both in vitro and in vivo that the predicted interactions do take place. The ability to predict potential cross-talk prior to designing and constructing novel pathways or choosing a host organism is essential for the promise that phosphosignalling components hold for synthetic biology to be realised.

摘要

磷酸信号通路是合成生物学家寻找广泛的模块化组件的理想选择,这些组件可以用来构建。我们证明了可以在合成生物学中使用双组分系统。然而,它们的潜力受到宿主细胞中存在许多自身磷酸信号通路的限制,这些通路可能与引入的合成组件相互作用和串扰。在本文中,我们还展示了一种简单的生物信息学工具,可以帮助预测引入的和本地的双组分信号通路之间是否会发生种间串扰,并在体外和体内显示预测的相互作用确实会发生。在设计和构建新的通路或选择宿主生物之前,预测潜在的串扰的能力对于实现磷酸信号组件在合成生物学中的应用至关重要。