Mutation of HIV-1 Genomes in a Clinical Population Treated with the Mutagenic Nucleoside KP1461
The deoxycytidine analog KP1212, and its prodrug KP1461, are prototypes of a new class of antiretroviral drugs designed to increase viral mutation rates, with the goal of eventually causing the collapse of the viral population. Here we present an extensive analysis of viral sequences from HIV-1 infe...
Main Authors: | Mullins, James I., Heath, Laura, Hughes, James P., Kicha, Jessica, Styrchak, Sheila, Wong, Kim G., Rao, Ushnal, Hansen, Alexis, Harris, Kevin S., Laurent, Jean-Pierre, Li, Deyu, Simpson, Jeffrey H., Essigmann, John M., Loeb, Lawrence A., Parkins, Jeffrey |
---|---|
Other Authors: | Massachusetts Institute of Technology. Department of Biological Engineering |
Format: | Article |
Language: | en_US |
Published: |
Public Library of Science
2011
|
Online Access: | http://hdl.handle.net/1721.1/65401 https://orcid.org/0000-0002-2196-5691 |
Similar Items
-
Tautomerism provides a molecular explanation for the mutagenic properties of the anti-HIV nucleoside 5-aza-5,6-dihydro-2'-deoxycytidine
by: Li, Deyu, et al.
Published: (2015) -
Two-dimensional IR spectroscopy of the anti-HIV agent KP1212 reveals protonated and neutral tautomers that influence pH-dependent mutagenicity
by: Peng, Chunte, et al.
Published: (2015) -
Tanúnévsor 1461-ből
by: Krisztina Fügedi
Published: (2001-12-01) -
Intrinsic mutagenic properties of 5-chlorocytosine: A mechanistic connection between chronic inflammation and cancer
by: Fedeles, Bogdan I., et al.
Published: (2016) -
Implications for Damage Recognition during Dpo4-Mediated Mutagenic Bypass of m1G and m3C Lesions
by: Rechkoblit, Olga, et al.
Published: (2014)