Literature DB >> 32690266

4'-C-Aminomethyl-2'-deoxy-2'-fluoroarabinonucleoside increases the nuclease resistance of DNA without inhibiting the ability of a DNA/RNA duplex to activate RNase H.

Tatsuya Tsuchihira1, Ryohei Kajino1, Yusuke Maeda1, Yoshihito Ueno2.   

Abstract

An antisense oligonucleotide is expected as an innovative drug for cancer and hereditary diseases. In this paper, we designed and synthesized DNAs containing a novel nucleoside analog, 1-(4-C-aminomethyl-2-deoxy-2-fluoro-β-d-arabinofuranosyl)thymine, and evaluated their properties. It was revealed that the analog slightly decreases the thermal stability of the DNA/RNA duplex but significantly increases the stability of DNA in a buffer containing bovine serum. Furthermore, it turned out that the DNA/RNA duplex containing the analog is a good substrate for Escherichia coli RNase H. Thus, DNAs containing the nucleoside analog would be good candidates for the development of therapeutic antisense oligonucleotides.
Copyright © 2020 Elsevier Ltd. All rights reserved.

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Keywords:  2′-deoxy-2′-fluoro arabinonucleoside; 4′-aminoalkyl group; Antisense oligonucleotide; Nuclease resistance; RNase H; Thermal stability

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Year:  2020        PMID: 32690266     DOI: 10.1016/j.bmc.2020.115611

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  1 in total

1.  Synthesis and evaluation of (S)-5'-C-aminopropyl and (S)-5'-C-aminopropyl-2'-arabinofluoro modified DNA oligomers for novel RNase H-dependent antisense oligonucleotides.

Authors:  Yujun Zhou; Ryohei Kajino; Seiichiro Ishii; Kenji Yamagishi; Yoshihito Ueno
Journal:  RSC Adv       Date:  2020-11-17       Impact factor: 4.036

  1 in total

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