• 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

RNA和核糖核蛋白作为合成生物学中的新型分子部件。

RNA and RNP as new molecular parts in synthetic biology.

作者信息

Saito Hirohide, Inoue Tan

机构信息

Department of Gene Mechanisms, Graduate School of Biostudies, Kyoto University, Kyoto 606-8502, Japan; ICORP, Japan Science and Technology Corporation (JST), Honcho, Kawaguchi-shi, Saitama 332-0012, Japan.

出版信息

J Biotechnol. 2007 Oct 15;132(1):1-7. doi: 10.1016/j.jbiotec.2007.07.952. Epub 2007 Aug 8.

DOI:10.1016/j.jbiotec.2007.07.952
PMID:17875338
Abstract

Synthetic biology has a promising outlook in biotechnology and for understanding the self-organizing principle of biological molecules in life. However, synthetic biologists have been looking for new molecular "parts" that function as modular units required in designing and constructing new "devices" and "systems" for regulating cell function because the number of such parts is strictly limited at present. In this review, we focus on RNA/ribonucleoprotein (RNP) architectures that hold promise as new "parts" for synthetic biology. They are constructed with molecular design and an experimental evolution technique. So far, designed self-folding RNAs, RNA (RNP) enzymes, and nanoscale RNA architectures have been successfully constructed by utilizing Watson-Crick base-pairs together with specific RNA-RNA or RNA-protein binding motifs of known defined 3D structures. Riboregulators for regulating targeted gene expression have also been designed and produced in vitro as well as in vivo. Lately, RNA and ribonucleoprotein complexes have been strongly attracting the attention of molecular biologists because a variety of noncoding RNAs discovered in nature perform spatiotemporal gene expressions. Thus we hope that newly accumulating knowledge on naturally occurring RNAs and RNP complexes will provide a variety of new parts, devices and systems for synthetic biology.

摘要

合成生物学在生物技术以及理解生命中生物分子的自组织原理方面有着广阔的前景。然而,合成生物学家一直在寻找新的分子“部件”,这些部件可作为设计和构建用于调节细胞功能的新“装置”和“系统”所需的模块化单元,因为目前这类部件的数量极为有限。在本综述中,我们聚焦于有望成为合成生物学新“部件”的RNA/核糖核蛋白(RNP)结构。它们是通过分子设计和实验进化技术构建而成的。到目前为止,利用沃森-克里克碱基对以及已知明确三维结构的特定RNA-RNA或RNA-蛋白质结合基序,已成功构建出设计的自折叠RNA、RNA(RNP)酶和纳米级RNA结构。用于调节靶向基因表达的核糖调节因子也已在体外和体内设计并产生。最近,RNA和核糖核蛋白复合物强烈吸引了分子生物学家的关注,因为自然界中发现的多种非编码RNA执行着时空基因表达。因此,我们希望新积累的关于天然存在的RNA和RNP复合物的知识能为合成生物学提供各种新的部件、装置和系统。

相似文献

1
RNA and RNP as new molecular parts in synthetic biology.RNA和核糖核蛋白作为合成生物学中的新型分子部件。
J Biotechnol. 2007 Oct 15;132(1):1-7. doi: 10.1016/j.jbiotec.2007.07.952. Epub 2007 Aug 8.
2
Synthetic biology with RNA motifs.具有RNA基序的合成生物学。
Int J Biochem Cell Biol. 2009 Feb;41(2):398-404. doi: 10.1016/j.biocel.2008.08.017. Epub 2008 Aug 19.
3
Folding RNA-Protein Complex into Designed Nanostructures.将RNA-蛋白质复合物折叠成设计好的纳米结构。
Methods Mol Biol. 2015;1316:169-79. doi: 10.1007/978-1-4939-2730-2_14.
4
Structure-function relationships in RNA and RNP enzymes: recent advances.RNA和核糖核蛋白(RNP)酶中的结构-功能关系:最新进展
Biopolymers. 2007;87(5-6):317-28. doi: 10.1002/bip.20836.
5
Generation of a catalytic module on a self-folding RNA.在自我折叠RNA上生成催化模块。
RNA. 2004 Dec;10(12):1900-6. doi: 10.1261/rna.7170304. Epub 2004 Nov 3.
6
Design and development of a catalytic ribonucleoprotein.催化核糖核蛋白的设计与开发
EMBO J. 2001 Oct 1;20(19):5453-60. doi: 10.1093/emboj/20.19.5453.
7
Evolution of biological catalysis: ribozyme to RNP enzyme.生物催化的进化:从核酶到核糖核蛋白酶
Cold Spring Harb Symp Quant Biol. 2009;74:11-6. doi: 10.1101/sqb.2009.74.024. Epub 2009 Oct 22.
8
RNA recognition by RNP proteins during RNA processing.RNA加工过程中RNP蛋白对RNA的识别
Annu Rev Biophys Biomol Struct. 1998;27:407-45. doi: 10.1146/annurev.biophys.27.1.407.
9
Ligand-dependent regulatory RNA parts for Synthetic Biology in eukaryotes.真核生物合成生物学中的配体依赖性调控 RNA 元件。
Curr Opin Biotechnol. 2010 Dec;21(6):760-5. doi: 10.1016/j.copbio.2010.06.010. Epub 2010 Jul 16.
10
Designed RNAs with two peptide-binding units as artificial templates for native chemical ligation of RNA-binding peptides.设计带有两个肽结合单元的 RNA 作为 RNA 结合肽的天然化学连接的人工模板。
Chembiochem. 2009 Nov 23;10(17):2745-52. doi: 10.1002/cbic.200900392.

引用本文的文献

1
Triggering RNAi with multifunctional RNA nanoparticles and their delivery.利用多功能RNA纳米颗粒触发RNA干扰及其递送
DNA RNA Nanotechnol. 2015 Jan;2(1):1-12. doi: 10.1515/rnan-2015-0001. Epub 2015 Jul 27.
2
Modulating Immune Response with Nucleic Acid Nanoparticles.用核酸纳米颗粒调节免疫反应。
Molecules. 2019 Oct 17;24(20):3740. doi: 10.3390/molecules24203740.
3
Responsive self-assembly of tectoRNAs with loop-receptor interactions from the tetrahydrofolate (THF) riboswitch.四氢叶酸(THF)核糖开关中环受体相互作用的 tectoRNA 响应性自组装。
Nucleic Acids Res. 2019 Jul 9;47(12):6439-6451. doi: 10.1093/nar/gkz304.
4
Versatile RNA tetra-U helix linking motif as a toolkit for nucleic acid nanotechnology.多功能RNA四聚体U螺旋连接基序作为核酸纳米技术的一种工具
Nanomedicine. 2017 Apr;13(3):1137-1146. doi: 10.1016/j.nano.2016.12.018. Epub 2017 Jan 4.
5
RNA-based gene circuits for cell regulation.用于细胞调控的基于RNA的基因回路。
Proc Jpn Acad Ser B Phys Biol Sci. 2016;92(9):412-422. doi: 10.2183/pjab.92.412.
6
RNA modularity for synthetic biology.用于合成生物学的RNA模块化
F1000Prime Rep. 2013 Nov 1;5:46. doi: 10.12703/P5-46. eCollection 2013.
7
Synthetic human cell fate regulation by protein-driven RNA switches.通过蛋白质驱动的RNA开关进行合成人类细胞命运调控。
Nat Commun. 2011 Jan 18;2:160. doi: 10.1038/ncomms1157.
8
Synthetic RNA-protein complex shaped like an equilateral triangle.三角形等边的 RNA-蛋白质合成复合物。
Nat Nanotechnol. 2011 Feb;6(2):116-20. doi: 10.1038/nnano.2010.268. Epub 2011 Jan 16.
9
Promoting RNA helical stacking via A-minor junctions.通过 A- 小沟结促进 RNA 螺旋堆积。
Nucleic Acids Res. 2011 Feb;39(3):1066-80. doi: 10.1093/nar/gkq748. Epub 2010 Sep 28.
10
A polyhedron made of tRNAs.由 tRNA 构成的多面体。
Nat Chem. 2010 Sep;2(9):772-9. doi: 10.1038/nchem.733. Epub 2010 Jul 18.