• 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

核酸与蛋白质的交联。修饰的聚腺苷酸作为大肠杆菌核糖体的信使核糖核酸。

Cross-linking of nucleic acids to proteins. Modified poly(A) as mRNA for Escherichia coli ribosomes.

作者信息

Wojtech E, Brimacombe R, Häckel A, Prochnow D, Fasold H

机构信息

Institut für Biochemie, J. W. Goethe-Universität Frankfurt, Germany.

出版信息

Eur J Biochem. 1994 Aug 1;223(3):799-803. doi: 10.1111/j.1432-1033.1994.tb19055.x.

DOI:10.1111/j.1432-1033.1994.tb19055.x
PMID:8055956
Abstract

Poly(adenylic acid) was modified by methylchlorotetrolic ester in a reproducible and defined content of the derivatized bases. The nucleic acid derivative is protein reactive and was coupled to 70S ribosomes from Escherichia coli, in order to identify proteins along the mRNA pathway. The binding of the label becomes specific under the direction of tRNA(Lys) and is then almost exclusively located on the small subunit. The proteins S1, S12, S18 and S21 were labeled, as shown by an antibody assay. The yield of the affinity label was 5.4%, as calculated from the labeled nucleic acid. This compares favourably with the yields from photolabile compounds.

摘要

聚腺苷酸通过甲基氯代四醇酯进行修饰,修饰碱基的含量具有可重复性和确定性。该核酸衍生物具有蛋白质反应活性,并与大肠杆菌的70S核糖体偶联,以鉴定沿mRNA途径的蛋白质。在tRNA(Lys)的指导下,标记物的结合变得具有特异性,然后几乎只位于小亚基上。抗体检测表明,蛋白质S1、S12、S18和S21被标记。根据标记的核酸计算,亲和标记的产率为5.4%。这与光不稳定化合物的产率相比具有优势。

相似文献

1
Cross-linking of nucleic acids to proteins. Modified poly(A) as mRNA for Escherichia coli ribosomes.核酸与蛋白质的交联。修饰的聚腺苷酸作为大肠杆菌核糖体的信使核糖核酸。
Eur J Biochem. 1994 Aug 1;223(3):799-803. doi: 10.1111/j.1432-1033.1994.tb19055.x.
2
Affinity labelling in situ of the bL12 protein on E. coli 70S ribosomes by means of a tRNA dialdehyde derivative.通过一种tRNA二醛衍生物对大肠杆菌70S核糖体上的bL12蛋白进行原位亲和标记。
J Biochem. 2017 Dec 1;162(6):437-448. doi: 10.1093/jb/mvx055.
3
Identification of the Escherichia coli 30S ribosomal subunit protein neighboring mRNA during initiation of translation.翻译起始过程中与大肠杆菌30S核糖体亚基蛋白相邻的mRNA的鉴定。
Biochimie. 1992 Apr;74(4):363-71. doi: 10.1016/0300-9084(92)90114-t.
4
Site-directed cross-linking studies on the E. coli tRNA-ribosome complex: determination of sites labelled with an aromatic azide attached to the variable loop or aminoacyl group of tRNA.大肠杆菌tRNA-核糖体复合物的定点交联研究:确定用连接于tRNA可变环或氨酰基的芳香叠氮化物标记的位点。
Nucleic Acids Res. 1993 Feb 25;21(4):887-96. doi: 10.1093/nar/21.4.887.
5
Conformational change in the 16S rRNA in the Escherichia coli 70S ribosome induced by P/P- and P/E-site tRNAPhe binding.P/P-和P/E位点苯丙氨酸转运RNA(tRNAPhe)结合诱导大肠杆菌70S核糖体中16S核糖体RNA的构象变化。
Biochemistry. 2003 Dec 16;42(49):14386-96. doi: 10.1021/bi035369q.
6
Identification of cysteine-10 of protein S18 as part of the mRNA-binding site of Escherichia coli ribosomes by affinity-labeling studies with a chemically reactive A-U-G analog.通过使用化学反应性A-U-G类似物进行亲和标记研究,鉴定出蛋白质S18的半胱氨酸-10是大肠杆菌核糖体mRNA结合位点的一部分。
Eur J Biochem. 1978 Dec 1;92(1):243-51. doi: 10.1111/j.1432-1033.1978.tb12742.x.
7
Structural arrangement of tRNA binding sites on Escherichia coli ribosomes, as revealed from data on affinity labelling with photoactivatable tRNA derivatives.从用可光活化的tRNA衍生物进行亲和标记的数据揭示的大肠杆菌核糖体上tRNA结合位点的结构排列。
Biochim Biophys Acta. 1989 Jul 7;1008(2):146-56. doi: 10.1016/0167-4781(80)90002-0.
8
Three-dimensional placement of the conserved 530 loop of 16 S rRNA and of its neighboring components in the 30 S subunit.16 S核糖体RNA保守的530环及其相邻组分在30 S亚基中的三维定位。
J Mol Biol. 1999 Feb 19;286(2):521-40. doi: 10.1006/jmbi.1998.2493.
9
Covalent cross-linking of poly(A) to Escherichia coli ribosomes, and localization of the cross-link site within the 16S RNA.聚腺苷酸与大肠杆菌核糖体的共价交联,以及交联位点在16S RNA中的定位。
Nucleic Acids Res. 1988 Mar 25;16(6):2369-88. doi: 10.1093/nar/16.6.2369.
10
Photoaffinity labeling of 30S-subunit proteins S7 and S11 by 4-thiouridine-substituted tRNA(Phe) situated at the P site of Escherichia coli ribosomes.位于大肠杆菌核糖体P位点的4-硫代尿苷取代的tRNA(苯丙氨酸)对30S亚基蛋白S7和S11进行光亲和标记。
RNA. 1997 Sep;3(9):1028-36.