HIV-1 drug discovery: targeting folded RNA structures with branched peptides
dc.contributor.author | Wynn, Jessica E. | en |
dc.contributor.author | Santos, Webster L. | en |
dc.contributor.department | Chemistry | en |
dc.contributor.department | Center for Drug Discovery | en |
dc.date.accessed | 2016-03-17 | en |
dc.date.accessioned | 2016-03-18T22:24:56Z | en |
dc.date.available | 2016-03-18T22:24:56Z | en |
dc.date.issued | 2015-04-28 | en |
dc.description.abstract | Human immunodeficiency virus type 1 (HIV-1) is an RNA virus that is prone to high rates of mutation. While the disease is managed with current antiretroviral therapies, drugs with a new mode of action are needed. A strategy towards this goal is aimed at targeting the native three-dimensional fold of conserved RNA structures. This perspective highlights medium-sized peptides and peptidomimetics used to target two conserved RNA structures of HIV-1. In particular, branched peptides have the capacity to bind in a multivalent fashion, utilizing a large surface area to achieve the necessary affinity and selectivity toward the target RNA. | en |
dc.description.notes | 2015 Royal Society of Chemistry Open Access Gold Article | en |
dc.description.sponsorship | National Institutes of Health (U.S.) | en |
dc.description.sponsorship | National Institute of General Medical Sciences (U.S.) | en |
dc.format.extent | 11 pages | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.citation | Wynn, J. E., & Santos, W. L. (2015). HIV-1 drug discovery: targeting folded RNA structures with branched peptides. Organic & Biomolecular Chemistry, 13(21), 5848-5858. doi:10.1039/C5OB00589B | en |
dc.identifier.doi | https://doi.org/10.1039/C5OB00589B | en |
dc.identifier.issn | 1477-0520 | en |
dc.identifier.issue | 21 | en |
dc.identifier.other | 2015_Wynn_HIV_1_drug_discovery_targeting_fold.pdf | en |
dc.identifier.other | GM093834 | en |
dc.identifier.uri | http://hdl.handle.net/10919/64968 | en |
dc.identifier.volume | 13 | en |
dc.language.iso | en_US | en |
dc.publisher | The Royal Society of Chemistry | en |
dc.rights | Creative Commons Attribution-NonCommercial 3.0 Unported | en |
dc.rights.uri | http://creativecommons.org/licenses/by-nc/3.0/ | en |
dc.title | HIV-1 drug discovery: targeting folded RNA structures with branched peptides | en |
dc.title.serial | Organic & Biomolecular Chemistry | en |
dc.type | Article - Refereed | en |
dc.type.dcmitype | Text | en |
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