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A high-throughput screening assay for eukaryotic elongation factor 2 kinase inhibitors
Eukaryotic elongation factor 2 kinase (eEF2K) inhibitors may aid in the development of new therapeutic agents to combat cancer. Purified human eEF2K was obtained from an Escherichia coli expression system and a luminescence-based high-throughput screening (HTS) assay was developed using MH-1 peptide...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5071636/ https://www.ncbi.nlm.nih.gov/pubmed/27818922 http://dx.doi.org/10.1016/j.apsb.2016.04.002 |
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author | Xiao, Ting Liu, Rui Proud, Christopher G. Wang, Ming-Wei |
author_facet | Xiao, Ting Liu, Rui Proud, Christopher G. Wang, Ming-Wei |
author_sort | Xiao, Ting |
collection | PubMed |
description | Eukaryotic elongation factor 2 kinase (eEF2K) inhibitors may aid in the development of new therapeutic agents to combat cancer. Purified human eEF2K was obtained from an Escherichia coli expression system and a luminescence-based high-throughput screening (HTS) assay was developed using MH-1 peptide as the substrate. The luminescent readouts correlated with the amount of adenosine triphosphate remaining in the kinase reaction. This method was applied to a large-scale screening campaign against a diverse compound library and subsequent confirmation studies. Nine initial hits showing inhibitory activities on eEF2K were identified from 56,000 synthetic compounds during the HTS campaign, of which, five were chosen to test their effects in cancer cell lines. |
format | Online Article Text |
id | pubmed-5071636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-50716362016-11-04 A high-throughput screening assay for eukaryotic elongation factor 2 kinase inhibitors Xiao, Ting Liu, Rui Proud, Christopher G. Wang, Ming-Wei Acta Pharm Sin B Original Article Eukaryotic elongation factor 2 kinase (eEF2K) inhibitors may aid in the development of new therapeutic agents to combat cancer. Purified human eEF2K was obtained from an Escherichia coli expression system and a luminescence-based high-throughput screening (HTS) assay was developed using MH-1 peptide as the substrate. The luminescent readouts correlated with the amount of adenosine triphosphate remaining in the kinase reaction. This method was applied to a large-scale screening campaign against a diverse compound library and subsequent confirmation studies. Nine initial hits showing inhibitory activities on eEF2K were identified from 56,000 synthetic compounds during the HTS campaign, of which, five were chosen to test their effects in cancer cell lines. Elsevier 2016-11 2016-05-21 /pmc/articles/PMC5071636/ /pubmed/27818922 http://dx.doi.org/10.1016/j.apsb.2016.04.002 Text en © 2016 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Xiao, Ting Liu, Rui Proud, Christopher G. Wang, Ming-Wei A high-throughput screening assay for eukaryotic elongation factor 2 kinase inhibitors |
title | A high-throughput screening assay for eukaryotic elongation factor 2 kinase inhibitors |
title_full | A high-throughput screening assay for eukaryotic elongation factor 2 kinase inhibitors |
title_fullStr | A high-throughput screening assay for eukaryotic elongation factor 2 kinase inhibitors |
title_full_unstemmed | A high-throughput screening assay for eukaryotic elongation factor 2 kinase inhibitors |
title_short | A high-throughput screening assay for eukaryotic elongation factor 2 kinase inhibitors |
title_sort | high-throughput screening assay for eukaryotic elongation factor 2 kinase inhibitors |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5071636/ https://www.ncbi.nlm.nih.gov/pubmed/27818922 http://dx.doi.org/10.1016/j.apsb.2016.04.002 |
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