• 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

纳米级大小的孔与核糖体出口腔的入口大小相似,是大型 RNA 的一个常见特征。

Nanometer scale pores similar in size to the entrance of the ribosomal exit cavity are a common feature of large RNAs.

出版信息

RNA. 2013 Oct;19(10):1349-54. doi: 10.1261/rna.038828.113. Epub 2013 Aug 12.

DOI:10.1261/rna.038828.113
PMID:23940386
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3854525/
Abstract

The highly conserved peptidyl transferase center (PTC) of the ribosome contains an RNA pore that serves as the entrance to the exit tunnel. Analysis of available ribosome crystal structures has revealed the presence of multiple additional well-defined pores of comparable size in the ribosomal (rRNA) RNAs. These typically have dimensions of 1-2 nm, with a total area of ∼100 Å(2) or more, and most are associated with one or more ribosomal proteins. The PTC example and the other rRNA pores result from the packing of helices. However, in the non-PTC cases the nitrogenous bases do not protrude into the pore, thereby limiting the potential for hydrogen bonding within the pore. Instead, it is the RNA backbone that largely defines the pore likely resulting in a negatively charged environment. In many but not all cases, ribosomal proteins are associated with the pores to a greater or lesser extent. With the exception of the PTC case, the large subunit pores are not found in what are thought to be the evolutionarily oldest regions of the 23S rRNA. The unusual nature of the PTC pore may reflect a history of being created by hybridization between two or more RNAs early in evolution rather than simple folding of a single RNA. An initial survey of nonribosomal RNA crystal structures revealed additional pores, thereby showing that they are likely a general feature of RNA tertiary structure.

摘要

核糖体高度保守的肽基转移酶中心 (PTC) 包含一个 RNA 孔,作为出口隧道的入口。对现有核糖体晶体结构的分析揭示了核糖体 (rRNA) RNA 中存在多个大小相当的额外明确的孔。这些孔通常尺寸为 1-2nm,总面积约为 100Å2 或更大,大多数与一个或多个核糖体蛋白相关。PTC 示例和其他 rRNA 孔是由螺旋包装形成的。然而,在非 PTC 情况下,含氮碱基不会突入孔内,从而限制了孔内氢键的形成潜力。相反,RNA 骨架在很大程度上定义了孔,可能导致带负电荷的环境。在许多但不是所有情况下,核糖体蛋白或多或少地与孔相关联。除了 PTC 情况外,大亚基孔不存在于被认为是 23S rRNA 中进化最古老的区域。PTC 孔的异常性质可能反映了在进化早期由两个或多个 RNA 杂交而不是单个 RNA 折叠形成的历史。对非核糖体 RNA 晶体结构的初步调查揭示了其他孔,从而表明它们可能是 RNA 三级结构的普遍特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0b9/3854525/7061084c8849/1349fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0b9/3854525/b5f26d1e763b/1349fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0b9/3854525/874c205d9bcf/1349fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0b9/3854525/7061084c8849/1349fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0b9/3854525/b5f26d1e763b/1349fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0b9/3854525/874c205d9bcf/1349fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0b9/3854525/7061084c8849/1349fig3.jpg

相似文献

1
Nanometer scale pores similar in size to the entrance of the ribosomal exit cavity are a common feature of large RNAs.纳米级大小的孔与核糖体出口腔的入口大小相似,是大型 RNA 的一个常见特征。
RNA. 2013 Oct;19(10):1349-54. doi: 10.1261/rna.038828.113. Epub 2013 Aug 12.
2
The structural basis of ribosome activity in peptide bond synthesis.核糖体在肽键合成中活性的结构基础。
Science. 2000 Aug 11;289(5481):920-30. doi: 10.1126/science.289.5481.920.
3
Insights into substrate stabilization from snapshots of the peptidyl transferase center of the intact 70S ribosome.从完整70S核糖体肽基转移酶中心的快照中洞察底物稳定性。
Nat Struct Mol Biol. 2009 May;16(5):528-33. doi: 10.1038/nsmb.1577. Epub 2009 Apr 12.
4
Effect of antibiotics on large ribosomal subunit assembly reveals possible function of 5 S rRNA.抗生素对大核糖体亚基组装的影响揭示了5S rRNA的可能功能。
J Mol Biol. 1999 Sep 3;291(5):1025-34. doi: 10.1006/jmbi.1999.3030.
5
Changes in the level of poly(Phe) synthesis in Escherichia coli ribosomes containing mutants of L4 ribosomal protein from Thermus thermophilus can be explained by structural changes in the peptidyltransferase center: a molecular dynamics simulation analysis.含有嗜热栖热菌L4核糖体蛋白突变体的大肠杆菌核糖体中多聚(苯丙氨酸)合成水平的变化,可以通过肽基转移酶中心的结构变化来解释:分子动力学模拟分析。
Eur Biophys J. 2006 Oct;35(8):675-83. doi: 10.1007/s00249-006-0076-4. Epub 2006 Jun 14.
6
Madumycin II inhibits peptide bond formation by forcing the peptidyl transferase center into an inactive state.麦迪霉素II通过迫使肽基转移酶中心进入无活性状态来抑制肽键形成。
Nucleic Acids Res. 2017 Jul 7;45(12):7507-7514. doi: 10.1093/nar/gkx413.
7
Sequence and structural conservation in RNA ribose zippers.RNA核糖拉链中的序列与结构保守性
J Mol Biol. 2002 Jul 12;320(3):455-74. doi: 10.1016/s0022-2836(02)00515-6.
8
The 3D arrangement of the 23 S and 5 S rRNA in the Escherichia coli 50 S ribosomal subunit based on a cryo-electron microscopic reconstruction at 7.5 A resolution.基于7.5埃分辨率的冷冻电子显微镜重建,大肠杆菌50S核糖体亚基中23S和5S rRNA的三维排列。
J Mol Biol. 2000 Apr 21;298(1):35-59. doi: 10.1006/jmbi.2000.3635.
9
A recurrent magnesium-binding motif provides a framework for the ribosomal peptidyl transferase center.一个重复的镁结合基序为核糖体肽基转移酶中心提供了一个框架。
Nucleic Acids Res. 2009 Jun;37(10):3134-42. doi: 10.1093/nar/gkp119. Epub 2009 Mar 11.
10
RMF inactivates ribosomes by covering the peptidyl transferase centre and entrance of peptide exit tunnel.核糖体挽救因子(RMF)通过覆盖肽基转移酶中心和肽出口通道的入口来使核糖体失活。
Genes Cells. 2004 Apr;9(4):271-8. doi: 10.1111/j.1356-9597.2004.00723.x.

引用本文的文献

1
The Expanding Universe of Extensions and Tails: Ribosomal Proteins and Histones in RNA and DNA Complex Signaling and Dynamics.扩展与尾巴的不断扩展的宇宙:核糖体蛋白和组蛋白在RNA和DNA复杂信号传导与动力学中的作用
Genes (Basel). 2025 Jan 1;16(1):45. doi: 10.3390/genes16010045.
2
The Peptidyl Transferase Center: a Window to the Past.肽基转移酶中心:洞察过去的窗口。
Microbiol Mol Biol Rev. 2021 Dec 15;85(4):e0010421. doi: 10.1128/MMBR.00104-21. Epub 2021 Nov 10.
3
Further Characterization of the Pseudo-Symmetrical Ribosomal Region.伪对称核糖体区域的进一步表征

本文引用的文献

1
Secondary structure and domain architecture of the 23S and 5S rRNAs.23S 和 5S rRNA 的二级结构和结构域结构。
Nucleic Acids Res. 2013 Aug;41(15):7522-35. doi: 10.1093/nar/gkt513. Epub 2013 Jun 14.
2
An exit cavity was crucial to the polymerase activity of the early ribosome.出口腔对于早期核糖体的聚合酶活性至关重要。
Astrobiology. 2012 Jan;12(1):57-60. doi: 10.1089/ast.2011.0692. Epub 2011 Dec 22.
3
The 2'-OH group of the peptidyl-tRNA stabilizes an active conformation of the ribosomal PTC.肽酰-tRNA 的 2'-OH 基团稳定了核糖体 PTC 的活性构象。
Life (Basel). 2020 Sep 14;10(9):201. doi: 10.3390/life10090201.
EMBO J. 2011 May 6;30(12):2445-53. doi: 10.1038/emboj.2011.142.
4
The mechanism of peptidyl transfer catalysis by the ribosome.核糖体介导的肽酰转移催化机制。
Annu Rev Biochem. 2011;80:527-55. doi: 10.1146/annurev-biochem-082108-165150.
5
Origin and evolution of the ribosome.核糖体的起源与进化。
Cold Spring Harb Perspect Biol. 2010 Sep;2(9):a003483. doi: 10.1101/cshperspect.a003483. Epub 2010 Jun 9.
6
Interplay between the ribosomal tunnel, nascent chain, and macrolides influences drug inhibition.核糖体通道、新生肽链和大环内酯类药物之间的相互作用会影响药物抑制作用。
Chem Biol. 2010 May 28;17(5):504-14. doi: 10.1016/j.chembiol.2010.04.008.
7
What recent ribosome structures have revealed about the mechanism of translation.近期核糖体结构揭示了关于翻译机制的哪些内容。
Nature. 2009 Oct 29;461(7268):1234-42. doi: 10.1038/nature08403. Epub 2009 Oct 18.
8
Peeling the onion: ribosomes are ancient molecular fossils.剖析根源:核糖体是古老的分子化石。
Mol Biol Evol. 2009 Nov;26(11):2415-25. doi: 10.1093/molbev/msp163. Epub 2009 Jul 23.
9
The evolving ribosome: from non-coded peptide bond formation to sophisticated translation machinery.不断进化的核糖体:从非编码肽键形成到精密的翻译机制。
Res Microbiol. 2009 Sep;160(7):487-92. doi: 10.1016/j.resmic.2009.07.004. Epub 2009 Jul 18.
10
Insights into substrate stabilization from snapshots of the peptidyl transferase center of the intact 70S ribosome.从完整70S核糖体肽基转移酶中心的快照中洞察底物稳定性。
Nat Struct Mol Biol. 2009 May;16(5):528-33. doi: 10.1038/nsmb.1577. Epub 2009 Apr 12.