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...
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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. |
doi_str_mv | 10.1038/srep29680 |
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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.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep29680</identifier><identifier>PMID: 27403722</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/1647/296 ; 631/45/320 ; 82/103 ; 82/16 ; 82/58 ; 96/34 ; Amino acids ; Chinese medicine ; Discriminant analysis ; Ebola virus ; Genomes ; Herbal medicine ; Humanities and Social Sciences ; Ligands ; Mass spectrometry ; multidisciplinary ; Natural resources ; Peptides ; Proteins ; RNA polymerase ; Science ; Scientific imaging ; Viruses</subject><ispartof>Scientific reports, 2016-07, Vol.6 (1), p.29680-29680, Article 29680</ispartof><rights>The Author(s) 2016</rights><rights>Copyright Nature Publishing Group Jul 2016</rights><rights>Copyright © 2016, Macmillan Publishers Limited 2016 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-1a4c0e2e05e31133f39011a1a55f92ee1b443ab8d2fb62c36d78ab121217f2933</citedby><cites>FETCH-LOGICAL-c438t-1a4c0e2e05e31133f39011a1a55f92ee1b443ab8d2fb62c36d78ab121217f2933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4940736/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4940736/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,42165,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27403722$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fu, Xu</creatorcontrib><creatorcontrib>Wang, Zhihua</creatorcontrib><creatorcontrib>Li, Lixin</creatorcontrib><creatorcontrib>Dong, Shishang</creatorcontrib><creatorcontrib>Li, Zhucui</creatorcontrib><creatorcontrib>Jiang, Zhenzuo</creatorcontrib><creatorcontrib>Wang, Yuefei</creatorcontrib><creatorcontrib>Shui, Wenqing</creatorcontrib><title>Novel Chemical Ligands to Ebola Virus and Marburg Virus Nucleoproteins Identified by Combining Affinity Mass Spectrometry and Metabolomics Approaches</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><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.</description><subject>631/1647/296</subject><subject>631/45/320</subject><subject>82/103</subject><subject>82/16</subject><subject>82/58</subject><subject>96/34</subject><subject>Amino acids</subject><subject>Chinese medicine</subject><subject>Discriminant analysis</subject><subject>Ebola virus</subject><subject>Genomes</subject><subject>Herbal medicine</subject><subject>Humanities and Social Sciences</subject><subject>Ligands</subject><subject>Mass spectrometry</subject><subject>multidisciplinary</subject><subject>Natural resources</subject><subject>Peptides</subject><subject>Proteins</subject><subject>RNA polymerase</subject><subject>Science</subject><subject>Scientific imaging</subject><subject>Viruses</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>BENPR</sourceid><recordid>eNplkU1r3DAQhk1paUKaQ_9AEfTSFLaRRvLXpbAsaRPYpod-XIUkj70KtuVKcmB_SP5vFXazbFrpoGHm0TszvFn2ltFPjPLqMnicoC4q-iI7BSryBXCAl0fxSXYewh1NJ4dasPp1dgKloLwEOM0ebt099mS1wcEa1ZO17dTYBBIdudKuV-S39XMgKUe-Ka9n3-0zt7Pp0U3eRbRjIDcNjtG2Fhuit2TlBm1HO3Zk2bYpiNv0OwTyY0ITvRsw-u1OE6NKbVxqHshySnLKbDC8yV61qg94vn_Psl9frn6urhfr719vVsv1wghexQVTwlAEpDlyxjhveU0ZU0zleVsDItNCcKWrBlpdgOFFU1ZKM0i3bKHm_Cz7vNOdZj1gY9IOXvVy8nZQfiudsvJ5ZbQb2bl7KWpBS14kgQ97Ae_-zBiiHGww2PdqRDcHySoqgEKRlwl9_w9652Y_pvUSxQBqVuU0URc7yngXkrXtYRhG5aPf8uB3Yt8dT38gn9xNwMcdEFJp7NAftfxP7S_anLax</recordid><startdate>20160712</startdate><enddate>20160712</enddate><creator>Fu, Xu</creator><creator>Wang, Zhihua</creator><creator>Li, Lixin</creator><creator>Dong, Shishang</creator><creator>Li, Zhucui</creator><creator>Jiang, Zhenzuo</creator><creator>Wang, Yuefei</creator><creator>Shui, Wenqing</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160712</creationdate><title>Novel Chemical Ligands to Ebola Virus and Marburg Virus Nucleoproteins Identified by Combining Affinity Mass Spectrometry and Metabolomics Approaches</title><author>Fu, Xu ; 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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.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>27403722</pmid><doi>10.1038/srep29680</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/1647/296 631/45/320 82/103 82/16 82/58 96/34 Amino acids Chinese medicine Discriminant analysis Ebola virus Genomes Herbal medicine Humanities and Social Sciences Ligands Mass spectrometry multidisciplinary Natural resources Peptides Proteins RNA polymerase Science Scientific imaging Viruses |
title | Novel Chemical Ligands to Ebola Virus and Marburg Virus Nucleoproteins Identified by Combining Affinity Mass Spectrometry and Metabolomics Approaches |
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