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HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity

West Nile virus (WNV) is a positive sense, single-stranded RNA virus that can cause illness in humans when transmitted via mosquito vectors. Unfortunately, no antivirals or vaccines are currently available, and therefore efficient and safe antivirals are urgently needed. We developed a high throughp...

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Autores principales: Chung, Dong Hoon, Jonsson, Colleen B., Maddox, Clinton, McKellip, Sara N., Moore, Blake. P., Heil, Marintha, White, E. Lucile, Ananthan, Subramaniam, Li, Qianjun, Feng, Shuang, Rasmussen, Lynn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839297/
https://www.ncbi.nlm.nih.gov/pubmed/20336008
http://dx.doi.org/10.3390/molecules15031690
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author Chung, Dong Hoon
Jonsson, Colleen B.
Maddox, Clinton
McKellip, Sara N.
Moore, Blake. P.
Heil, Marintha
White, E. Lucile
Ananthan, Subramaniam
Li, Qianjun
Feng, Shuang
Rasmussen, Lynn
author_facet Chung, Dong Hoon
Jonsson, Colleen B.
Maddox, Clinton
McKellip, Sara N.
Moore, Blake. P.
Heil, Marintha
White, E. Lucile
Ananthan, Subramaniam
Li, Qianjun
Feng, Shuang
Rasmussen, Lynn
author_sort Chung, Dong Hoon
collection PubMed
description West Nile virus (WNV) is a positive sense, single-stranded RNA virus that can cause illness in humans when transmitted via mosquito vectors. Unfortunately, no antivirals or vaccines are currently available, and therefore efficient and safe antivirals are urgently needed. We developed a high throughput screen to discover small molecule probes that inhibit virus infection of Vero E6 cells. A primary screen of a 13,001 compound library at a 10 μM final concentration was conducted using the 384-well format. Z′ values ranged from 0.54–0.83 with a median of 0.74. Average S/B was 17 and S/N for each plate ranged from 10.8 to 23.9. Twenty-six compounds showed a dose response in the HT screen and were further evaluated in a time of addition assay and in a titer reduction assay. Seven compounds showed potential as small molecule probes directed at WNV. The hit rate from the primary screen was 0.185% (24 compounds out of 13,001 compounds) and from the secondary screens was 0.053% (7 out of 13,001 compounds) respectively.
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spelling pubmed-48392972016-04-21 HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity Chung, Dong Hoon Jonsson, Colleen B. Maddox, Clinton McKellip, Sara N. Moore, Blake. P. Heil, Marintha White, E. Lucile Ananthan, Subramaniam Li, Qianjun Feng, Shuang Rasmussen, Lynn Molecules Article West Nile virus (WNV) is a positive sense, single-stranded RNA virus that can cause illness in humans when transmitted via mosquito vectors. Unfortunately, no antivirals or vaccines are currently available, and therefore efficient and safe antivirals are urgently needed. We developed a high throughput screen to discover small molecule probes that inhibit virus infection of Vero E6 cells. A primary screen of a 13,001 compound library at a 10 μM final concentration was conducted using the 384-well format. Z′ values ranged from 0.54–0.83 with a median of 0.74. Average S/B was 17 and S/N for each plate ranged from 10.8 to 23.9. Twenty-six compounds showed a dose response in the HT screen and were further evaluated in a time of addition assay and in a titer reduction assay. Seven compounds showed potential as small molecule probes directed at WNV. The hit rate from the primary screen was 0.185% (24 compounds out of 13,001 compounds) and from the secondary screens was 0.053% (7 out of 13,001 compounds) respectively. Molecular Diversity Preservation International 2010-03-12 /pmc/articles/PMC4839297/ /pubmed/20336008 http://dx.doi.org/10.3390/molecules15031690 Text en © 2010 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Chung, Dong Hoon
Jonsson, Colleen B.
Maddox, Clinton
McKellip, Sara N.
Moore, Blake. P.
Heil, Marintha
White, E. Lucile
Ananthan, Subramaniam
Li, Qianjun
Feng, Shuang
Rasmussen, Lynn
HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity
title HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity
title_full HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity
title_fullStr HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity
title_full_unstemmed HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity
title_short HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity
title_sort hts-driven discovery of new chemotypes with west nile virus inhibitory activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839297/
https://www.ncbi.nlm.nih.gov/pubmed/20336008
http://dx.doi.org/10.3390/molecules15031690
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