Cargando…
Novel Chemical Ligands to Ebola Virus and Marburg Virus Nucleoproteins Identified by Combining Affinity Mass Spectrometry and Metabolomics Approaches
The nucleoprotein (NP) of Ebola virus (EBOV) and Marburg virus (MARV) is an essential component of the viral ribonucleoprotein complex and significantly impacts replication and transcription of the viral RNA genome. Although NP is regarded as a promising antiviral druggable target, no chemical ligan...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4940736/ https://www.ncbi.nlm.nih.gov/pubmed/27403722 http://dx.doi.org/10.1038/srep29680 |
_version_ | 1782442191114731520 |
---|---|
author | Fu, Xu Wang, Zhihua Li, Lixin Dong, Shishang Li, Zhucui Jiang, Zhenzuo Wang, Yuefei Shui, Wenqing |
author_facet | Fu, Xu Wang, Zhihua Li, Lixin Dong, Shishang Li, Zhucui Jiang, Zhenzuo Wang, Yuefei Shui, Wenqing |
author_sort | Fu, Xu |
collection | PubMed |
description | The nucleoprotein (NP) of Ebola virus (EBOV) and Marburg virus (MARV) is an essential component of the viral ribonucleoprotein complex and significantly impacts replication and transcription of the viral RNA genome. Although NP is regarded as a promising antiviral druggable target, no chemical ligands have been reported to interact with EBOV NP or MARV NP. We identified two compounds from a traditional Chinese medicine Gancao (licorice root) that can bind both NPs by combining affinity mass spectrometry and metabolomics approaches. These two ligands, 18β-glycyrrhetinic acid and licochalcone A, were verified by defined compound mixture screens and further characterized with individual ligand binding assays. Accompanying biophysical analyses demonstrate that binding of 18β-glycyrrhetinic acid to EBOV NP significantly reduces protein thermal stability, induces formation of large NP oligomers, and disrupts the critical association of viral ssRNA with NP complexes whereas the compound showed no such activity on MARV NP. Our study has revealed the substantial potential of new analytical techniques in ligand discovery from natural herb resources. In addition, identification of a chemical ligand that influences the oligomeric state and RNA-binding function of EBOV NP sheds new light on antiviral drug development. |
format | Online Article Text |
id | pubmed-4940736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49407362016-07-14 Novel Chemical Ligands to Ebola Virus and Marburg Virus Nucleoproteins Identified by Combining Affinity Mass Spectrometry and Metabolomics Approaches Fu, Xu Wang, Zhihua Li, Lixin Dong, Shishang Li, Zhucui Jiang, Zhenzuo Wang, Yuefei Shui, Wenqing Sci Rep Article The nucleoprotein (NP) of Ebola virus (EBOV) and Marburg virus (MARV) is an essential component of the viral ribonucleoprotein complex and significantly impacts replication and transcription of the viral RNA genome. Although NP is regarded as a promising antiviral druggable target, no chemical ligands have been reported to interact with EBOV NP or MARV NP. We identified two compounds from a traditional Chinese medicine Gancao (licorice root) that can bind both NPs by combining affinity mass spectrometry and metabolomics approaches. These two ligands, 18β-glycyrrhetinic acid and licochalcone A, were verified by defined compound mixture screens and further characterized with individual ligand binding assays. Accompanying biophysical analyses demonstrate that binding of 18β-glycyrrhetinic acid to EBOV NP significantly reduces protein thermal stability, induces formation of large NP oligomers, and disrupts the critical association of viral ssRNA with NP complexes whereas the compound showed no such activity on MARV NP. Our study has revealed the substantial potential of new analytical techniques in ligand discovery from natural herb resources. In addition, identification of a chemical ligand that influences the oligomeric state and RNA-binding function of EBOV NP sheds new light on antiviral drug development. Nature Publishing Group 2016-07-12 /pmc/articles/PMC4940736/ /pubmed/27403722 http://dx.doi.org/10.1038/srep29680 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Fu, Xu Wang, Zhihua Li, Lixin Dong, Shishang Li, Zhucui Jiang, Zhenzuo Wang, Yuefei Shui, Wenqing Novel Chemical Ligands to Ebola Virus and Marburg Virus Nucleoproteins Identified by Combining Affinity Mass Spectrometry and Metabolomics Approaches |
title | Novel Chemical Ligands to Ebola Virus and Marburg Virus Nucleoproteins Identified by Combining Affinity Mass Spectrometry and Metabolomics Approaches |
title_full | Novel Chemical Ligands to Ebola Virus and Marburg Virus Nucleoproteins Identified by Combining Affinity Mass Spectrometry and Metabolomics Approaches |
title_fullStr | Novel Chemical Ligands to Ebola Virus and Marburg Virus Nucleoproteins Identified by Combining Affinity Mass Spectrometry and Metabolomics Approaches |
title_full_unstemmed | Novel Chemical Ligands to Ebola Virus and Marburg Virus Nucleoproteins Identified by Combining Affinity Mass Spectrometry and Metabolomics Approaches |
title_short | Novel Chemical Ligands to Ebola Virus and Marburg Virus Nucleoproteins Identified by Combining Affinity Mass Spectrometry and Metabolomics Approaches |
title_sort | novel chemical ligands to ebola virus and marburg virus nucleoproteins identified by combining affinity mass spectrometry and metabolomics approaches |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4940736/ https://www.ncbi.nlm.nih.gov/pubmed/27403722 http://dx.doi.org/10.1038/srep29680 |
work_keys_str_mv | AT fuxu novelchemicalligandstoebolavirusandmarburgvirusnucleoproteinsidentifiedbycombiningaffinitymassspectrometryandmetabolomicsapproaches AT wangzhihua novelchemicalligandstoebolavirusandmarburgvirusnucleoproteinsidentifiedbycombiningaffinitymassspectrometryandmetabolomicsapproaches AT lilixin novelchemicalligandstoebolavirusandmarburgvirusnucleoproteinsidentifiedbycombiningaffinitymassspectrometryandmetabolomicsapproaches AT dongshishang novelchemicalligandstoebolavirusandmarburgvirusnucleoproteinsidentifiedbycombiningaffinitymassspectrometryandmetabolomicsapproaches AT lizhucui novelchemicalligandstoebolavirusandmarburgvirusnucleoproteinsidentifiedbycombiningaffinitymassspectrometryandmetabolomicsapproaches AT jiangzhenzuo novelchemicalligandstoebolavirusandmarburgvirusnucleoproteinsidentifiedbycombiningaffinitymassspectrometryandmetabolomicsapproaches AT wangyuefei novelchemicalligandstoebolavirusandmarburgvirusnucleoproteinsidentifiedbycombiningaffinitymassspectrometryandmetabolomicsapproaches AT shuiwenqing novelchemicalligandstoebolavirusandmarburgvirusnucleoproteinsidentifiedbycombiningaffinitymassspectrometryandmetabolomicsapproaches |