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Chemical Incorporation of Chain-Terminating Nucleoside Analogs as 3′-Blocking DNA Damage and Their Removal by Human ERCC1-XPF Endonuclease

Nucleoside/nucleotide analogs that lack the 3′-hydroxy group are widely utilized for HIV therapy. These chain-terminating nucleoside analogs (CTNAs) block DNA synthesis after their incorporation into growing DNA, leading to the antiviral effects. However, they are also considered to be DNA damaging...

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Bibliografske podrobnosti
izdano v:Molecules
Main Authors: Yamamoto, Junpei, Takahata, Chiaki, Kuraoka, Isao, Hirota, Kouji, Iwai, Shigenori
Format: Artigo
Jezik:Inglês
Izdano: MDPI 2016
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6273010/
https://ncbi.nlm.nih.gov/pubmed/27294910
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/molecules21060766
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