Synthesis and recognition of novel isonucleoside triphosphates by DNA polymerases
- PMID: 17320403
- DOI: 10.1016/j.bmc.2007.02.003
Synthesis and recognition of novel isonucleoside triphosphates by DNA polymerases
Abstract
Isonucleosides have been attracting a lot of attention in recent years due to the chemical and enzymatic stability and potential anticancer and antiviral activities. We have reported some of the isonucleosides which exhibited significant anticancer activity and found that the oligonucleotide incorporated with isonucleoside could increase the enzymatic stability against the degradation by phosphodiesterase. In this paper, we investigated the recognition of the isonucleoside triphosphates 1-6 by Taq, Vent(exo(-)), DeepVent(exo(-)), 9 degrees Nm, and Therminator DNA polymerases by a non-radioactivity method. We found that most of the isonucleoside triphosphates can be recognized by various DNA polymerase and act as terminators. Isonucleoside triphosphates 2 and 6 can be incorporated as substrates into the primer at 3' terminus to lengthen the chain dependent on a DNA template by Vent(exo(-)) and DeepVent(exo(-)) DNA polymerases.
Similar articles
-
Incorporation of 2'-deoxy-2'-isonucleoside 5'-triphosphates (iNTPs) into DNA by A- and B-family DNA polymerases with different recognition mechanisms.Chembiochem. 2010 Dec 10;11(18):2597-605. doi: 10.1002/cbic.201000449. Chembiochem. 2010. PMID: 21108267
-
2',3'-Dideoxy-3'-thionucleoside triphosphates: syntheses and polymerase substrate activities.Org Lett. 2007 Mar 15;9(6):1161-3. doi: 10.1021/ol070147w. Epub 2007 Feb 24. Org Lett. 2007. PMID: 17319676
-
Enzymatic polymerization of phosphonate nucleosides.Chembiochem. 2008 Nov 24;9(17):2883-8. doi: 10.1002/cbic.200800494. Chembiochem. 2008. PMID: 19006151
-
Rational design of polymerase inhibitors as antiviral drugs.Antiviral Res. 2006 Sep;71(2-3):90-5. doi: 10.1016/j.antiviral.2006.05.012. Epub 2006 Jun 6. Antiviral Res. 2006. PMID: 16820225 Review.
-
Fluorinated phosphonates: synthesis and biomedical application.Chem Rev. 2006 Sep;106(9):3868-935. doi: 10.1021/cr051000q. Chem Rev. 2006. PMID: 16967924 Review. No abstract available.
Cited by
-
Enzymatic synthesis of DNA strands containing α-L-LNA (α-L-configured locked nucleic acid) thymine nucleotides.Artif DNA PNA XNA. 2012 Jan-Mar;3(1):14-21. doi: 10.4161/adna.19272. Artif DNA PNA XNA. 2012. PMID: 22679529 Free PMC article.
-
Replicative bypass studies of l-deoxyribonucleosides in Vitro and in E. coli cell.Sci Rep. 2022 Dec 7;12(1):21183. doi: 10.1038/s41598-022-24802-5. Sci Rep. 2022. PMID: 36476762 Free PMC article.
-
Synthesis, physicochemical and biological properties of oligonucleotides incorporated with amino-isonucleosides.Sci China Chem. 2012;55(1):70-79. doi: 10.1007/s11426-011-4465-x. Epub 2011 Dec 2. Sci China Chem. 2012. PMID: 32214999 Free PMC article.
-
Compatibility and Fidelity of Mirror-Image Thymidine in Transcription Events by T7 RNA Polymerase.Mol Ther Nucleic Acids. 2020 Sep 4;21:604-613. doi: 10.1016/j.omtn.2020.06.023. Epub 2020 Jun 27. Mol Ther Nucleic Acids. 2020. PMID: 32721880 Free PMC article.
-
Synthesis and Biological Evaluation of Structurally Varied 5'-/6'-Isonucleosides and Theobromine-Containing N-Isonucleosidyl Derivatives.Pharmaceuticals (Basel). 2019 Jul 2;12(3):103. doi: 10.3390/ph12030103. Pharmaceuticals (Basel). 2019. PMID: 31269639 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources