• 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
Comprehensive analysis of the effects of Escherichia coli ORFs on protein translation reaction.大肠杆菌开放阅读框对蛋白质翻译反应影响的综合分析。
Mol Cell Proteomics. 2008 Aug;7(8):1530-40. doi: 10.1074/mcp.M800051-MCP200. Epub 2008 May 2.
2
Reaction dynamics analysis of a reconstituted protein translation system by computational modeling.通过计算建模对重组蛋白质翻译系统进行反应动力学分析。
Proc Natl Acad Sci U S A. 2017 Feb 21;114(8):E1336-E1344. doi: 10.1073/pnas.1615351114. Epub 2017 Feb 6.
3
In vivo effect of inactivation of ribosome recycling factor - fate of ribosomes after unscheduled translation downstream of open reading frame.核糖体循环因子失活的体内效应——开放阅读框下游非预定翻译后核糖体的命运
Mol Microbiol. 2004 Nov;54(4):1011-21. doi: 10.1111/j.1365-2958.2004.04324.x.
4
Identification of protein complexes and functional modules in E. coli PPI networks.鉴定大肠杆菌蛋白质相互作用网络中的蛋白质复合物和功能模块。
BMC Microbiol. 2020 Aug 6;20(1):243. doi: 10.1186/s12866-020-01904-6.
5
Translational Repression of the RpoS Antiadapter IraD by CsrA Is Mediated via Translational Coupling to a Short Upstream Open Reading Frame.CsrA通过与一个短的上游开放阅读框的翻译偶联介导对RpoS反适配器IraD的翻译抑制。
mBio. 2017 Aug 29;8(4):e01355-17. doi: 10.1128/mBio.01355-17.
6
[A model for trans-translation].[一种反式翻译模型]
Yi Chuan. 2006 Aug;28(8):1051-4.
7
Escherichia coli persister cells suppress translation by selectively disassembling and degrading their ribosomes.大肠杆菌持留菌通过选择性地拆解和降解其核糖体来抑制翻译。
Mol Microbiol. 2015 Jan;95(2):352-64. doi: 10.1111/mmi.12884. Epub 2014 Dec 19.
8
trans-translation-mediated tight regulation of the expression of the alternative ribosome-rescue factor ArfA in Escherichia coli.反式翻译介导的大肠杆菌中替代性核糖体拯救因子ArfA表达的严格调控
Genes Genet Syst. 2011;86(3):151-63. doi: 10.1266/ggs.86.151.
9
Identifying New Small Proteins in Escherichia coli.鉴定大肠杆菌中的新小蛋白。
Proteomics. 2018 May;18(10):e1700064. doi: 10.1002/pmic.201700064. Epub 2018 May 2.
10
The protein translation machinery is expressed for maximal efficiency in Escherichia coli.蛋白质翻译机制在大肠杆菌中表达以达到最高效率。
Nat Commun. 2020 Oct 16;11(1):5260. doi: 10.1038/s41467-020-18948-x.

引用本文的文献

1
The Long Road to a Synthetic Self-Replicating Central Dogma.通往合成自我复制中心法则的漫漫长路。
Biochemistry. 2023 Apr 4;62(7):1221-1232. doi: 10.1021/acs.biochem.3c00023. Epub 2023 Mar 21.
2
In vitro synthesis of 32 translation-factor proteins from a single template reveals impaired ribosomal processivity.从单个模板体外合成 32 种翻译因子蛋白,揭示了核糖体的进行性降低。
Sci Rep. 2021 Jan 21;11(1):1898. doi: 10.1038/s41598-020-80827-8.
3
Bottom-Up Construction of Complex Biomolecular Systems With Cell-Free Synthetic Biology.利用无细胞合成生物学自下而上构建复杂生物分子系统
Front Bioeng Biotechnol. 2020 Mar 24;8:213. doi: 10.3389/fbioe.2020.00213. eCollection 2020.
4
Self-replication of DNA by its encoded proteins in liposome-based synthetic cells.基于脂质体的人工细胞中,由其编码蛋白对 DNA 的自我复制。
Nat Commun. 2018 Apr 20;9(1):1583. doi: 10.1038/s41467-018-03926-1.
5
De novo design and synthesis of a 30-cistron translation-factor module.30个顺反子翻译因子模块的从头设计与合成。
Nucleic Acids Res. 2017 Oct 13;45(18):10895-10905. doi: 10.1093/nar/gkx753.
6
Dissecting limiting factors of the Protein synthesis Using Recombinant Elements (PURE) system.剖析使用重组元件的蛋白质合成(PURE)系统的限制因素。
Translation (Austin). 2017 May 9;5(1):e1327006. doi: 10.1080/21690731.2017.1327006. eCollection 2017.
7
Evolutionary Consequence of a Trade-Off between Growth and Maintenance along with Ribosomal Damages.生长与维持之间权衡以及核糖体损伤的进化后果。
PLoS One. 2015 Aug 20;10(8):e0135639. doi: 10.1371/journal.pone.0135639. eCollection 2015.
8
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.
9
Global analysis of chaperone effects using a reconstituted cell-free translation system.使用体外重组翻译系统进行伴侣蛋白效应的全局分析。
Proc Natl Acad Sci U S A. 2012 Jun 5;109(23):8937-42. doi: 10.1073/pnas.1201380109. Epub 2012 May 21.
10
Kinetic analysis of β-galactosidase and β-glucuronidase tetramerization coupled with protein translation.β-半乳糖苷酶和β-葡萄糖醛酸酶四聚体化与蛋白质翻译偶联的动力学分析。
J Biol Chem. 2011 Jun 24;286(25):22028-34. doi: 10.1074/jbc.M111.240168. Epub 2011 Apr 29.

本文引用的文献

1
Compensatory evolution of a WW domain variant lacking the strictly conserved Trp residue.缺乏严格保守色氨酸残基的WW结构域变体的补偿性进化。
J Mol Evol. 2008 Jan;66(1):61-71. doi: 10.1007/s00239-007-9061-5. Epub 2007 Dec 18.
2
prlF and yhaV encode a new toxin-antitoxin system in Escherichia coli.prlF和yhaV在大肠杆菌中编码一种新的毒素-抗毒素系统。
J Mol Biol. 2007 Sep 28;372(4):894-905. doi: 10.1016/j.jmb.2007.07.016. Epub 2007 Jul 21.
3
Relating three-dimensional structures to protein networks provides evolutionary insights.将三维结构与蛋白质网络联系起来可提供进化方面的见解。
Science. 2006 Dec 22;314(5807):1938-41. doi: 10.1126/science.1136174.
4
MBGD: a platform for microbial comparative genomics based on the automated construction of orthologous groups.MBGD:一个基于直系同源群自动构建的微生物比较基因组学平台。
Nucleic Acids Res. 2007 Jan;35(Database issue):D343-6. doi: 10.1093/nar/gkl978. Epub 2006 Nov 29.
5
Nascent chain, mRNA, and ribosome complexes generated by a pure translation system.由纯翻译系统产生的新生链、信使核糖核酸和核糖体复合物。
Biochem Biophys Res Commun. 2007 Jan 12;352(2):372-7. doi: 10.1016/j.bbrc.2006.11.050. Epub 2006 Nov 17.
6
The highly conserved LepA is a ribosomal elongation factor that back-translocates the ribosome.高度保守的 LepA 是一种使核糖体反向移位的核糖体延伸因子。
Cell. 2006 Nov 17;127(4):721-33. doi: 10.1016/j.cell.2006.09.037.
7
Femtoliter compartment in liposomes for in vitro selection of proteins.用于蛋白质体外筛选的脂质体中的飞升隔室。
Anal Biochem. 2006 Oct 1;357(1):128-36. doi: 10.1016/j.ab.2006.06.040. Epub 2006 Jul 18.
8
Evolutionary and physiological importance of hub proteins.枢纽蛋白的进化和生理重要性。
PLoS Comput Biol. 2006 Jul 14;2(7):e88. doi: 10.1371/journal.pcbi.0020088. Epub 2006 Jun 5.
9
Cell-free expression systems for eukaryotic protein production.用于真核蛋白质生产的无细胞表达系统。
Curr Opin Biotechnol. 2006 Aug;17(4):373-80. doi: 10.1016/j.copbio.2006.06.009. Epub 2006 Jul 7.
10
Complete set of ORF clones of Escherichia coli ASKA library (a complete set of E. coli K-12 ORF archive): unique resources for biological research.大肠杆菌ASKA文库的全套开放阅读框克隆(大肠杆菌K-12开放阅读框文库全集):生物学研究的独特资源。
DNA Res. 2005;12(5):291-9. doi: 10.1093/dnares/dsi012. Epub 2006 Jan 9.

大肠杆菌开放阅读框对蛋白质翻译反应影响的综合分析。

Comprehensive analysis of the effects of Escherichia coli ORFs on protein translation reaction.

作者信息

Kazuta Yasuaki, Adachi Jiro, Matsuura Tomoaki, Ono Naoaki, Mori Hirotada, Yomo Tetsuya

机构信息

Department of Bioinformatics Engineering, Osaka University, Japan.

出版信息

Mol Cell Proteomics. 2008 Aug;7(8):1530-40. doi: 10.1074/mcp.M800051-MCP200. Epub 2008 May 2.

DOI:10.1074/mcp.M800051-MCP200
PMID:18453339
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2500233/
Abstract

Protein synthesis is one of the most important reactions in the cell. Recent experimental studies indicated that this complex reaction can be achieved with a minimum complement of 36 proteins and ribosomes by reconstituting an Escherichia coli-based in vitro translation system with these protein components highly purified on an individual basis. From the protein-protein interaction (PPI) network of E. coli proteins, these minimal protein components are known to interact physically with large numbers of proteins. However, it is unclear what fraction of E. coli proteins are linked functionally with the minimal protein synthesis system. We investigated the effects of each of the 4194 E. coli ORF products on the minimal protein synthesis system; at least 12% of the entire ORF products, a significant fraction of the gene product of E. coli, affect the activity of this system. Furthermore 34% of these functional modifiers present in the PPI network were shown by mapping to be directly linked (i.e. to interact physically) with the minimal components of the PPI network. Topological analysis of the relationships between modifiers and the minimal components in the PPI network indicated clustering of the minimal components. The modifiers showed no such clustering, indicating that the location of functional modifiers is spread across the PPI network rather than clustering close to the minimal protein components. These observations may reflect the evolutionary process of the protein synthesis system.

摘要

蛋白质合成是细胞中最重要的反应之一。最近的实验研究表明,通过用逐个高度纯化的蛋白质组分重建基于大肠杆菌的体外翻译系统,仅需最少36种蛋白质和核糖体就能实现这一复杂反应。从大肠杆菌蛋白质的蛋白质 - 蛋白质相互作用(PPI)网络可知,这些最小蛋白质组分与大量蛋白质存在物理相互作用。然而,尚不清楚大肠杆菌中有多少比例的蛋白质与最小蛋白质合成系统存在功能联系。我们研究了4194种大肠杆菌开放阅读框(ORF)产物中的每一种对最小蛋白质合成系统的影响;至少12%的全部ORF产物(这是大肠杆菌基因产物的相当一部分)会影响该系统的活性。此外,通过图谱分析表明,PPI网络中34%的这些功能修饰因子与PPI网络的最小组分直接相连(即存在物理相互作用)。对PPI网络中修饰因子与最小组分之间关系的拓扑分析表明,最小组分存在聚类现象。修饰因子则没有这种聚类现象,这表明功能修饰因子的位置分布在整个PPI网络中,而非聚集在最小蛋白质组分附近。这些观察结果可能反映了蛋白质合成系统的进化过程。