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磷酸骨架对EcoRV限制性核酸内切酶识别和水解DNA的影响。一项使用寡脱氧核苷酸硫代磷酸酯的研究。

Influence of the phosphate backbone on the recognition and hydrolysis of DNA by the EcoRV restriction endonuclease. A study using oligodeoxynucleotide phosphorothioates.

作者信息

Thorogood H, Grasby J A, Connolly B A

机构信息

Department of Biochemistry and Genetics, University of Newcastle, Newcastle upon Tyne NE2 4HH, United Kingdom.

出版信息

J Biol Chem. 1996 Apr 12;271(15):8855-62. doi: 10.1074/jbc.271.15.8855.

Abstract

A set of phosphorothioate-containing oligonucleotides based on pGACGATATCGTC, a self-complementary dodecamer that contains the EcoRV recognition sequence (GATATC), has been prepared. The phosphorothioate group has been individually introduced at the central nine phosphate positions and the two diastereomers produced at each site separated and purified. The Km and Vmax values found for each of these modified DNA molecules with the EcoRV restriction endonuclease have been determined and compared with those seen for the unmodified all-phosphate-containing dodecamer. This has enabled an evaluation of the roles that both of the non-esterified oxygen atoms in the individual phosphates play in DNA binding and hydrolysis by the endonuclease. The results have also been compared with crystal structures of the EcoRV endonuclease, complexed with an oligodeoxynucleotide, to allow further definition of phosphate group function during substrate binding and turnover. For further study, see the related article "Probing the Indirect Readout of the Restriction Enzyme EcoRV: Mutational Analysis of Contacts to the DNA Backbone" (Wenz, A., Jeltsch, A., and Pingoud, A. (1996) J. Biol. Chem. 271, 5565-5573).

摘要

基于pGACGATATCGTC(一种包含EcoRV识别序列(GATATC)的自互补十二聚体)制备了一组含硫代磷酸酯的寡核苷酸。硫代磷酸酯基团已分别引入到中间的九个磷酸位置,并且在每个位点产生的两种非对映异构体已被分离和纯化。已测定了这些修饰的DNA分子中每一个与EcoRV限制性内切酶的Km和Vmax值,并与未修饰的全磷酸化十二聚体的相应值进行了比较。这使得能够评估单个磷酸酯中两个非酯化氧原子在DNA与内切酶结合及水解过程中所起的作用。研究结果还与EcoRV内切酶与寡脱氧核苷酸复合的晶体结构进行了比较,以便进一步明确底物结合和周转过程中磷酸基团的功能。欲了解更多研究内容,请参阅相关文章《探索限制性酶EcoRV的间接识别:与DNA主链接触的突变分析》(Wenz, A., Jeltsch, A., and Pingoud, A. (1996) J. Biol. Chem. 271, 5565 - 5573)。

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