Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/89971
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorTsang, TF-
dc.creatorQiu, Y-
dc.creatorLin, L-
dc.creatorYe, J-
dc.creatorMa, C-
dc.creatorYang, X-
dc.date.accessioned2021-05-13T08:33:08Z-
dc.date.available2021-05-13T08:33:08Z-
dc.identifier.urihttp://hdl.handle.net/10397/89971-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2019 American Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Infectious Diseases, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsinfecdis.9b00020.en_US
dc.subjectAntimicrobial agenten_US
dc.subjectBacterial transcriptionen_US
dc.subjectIn vitro drug screeningen_US
dc.subjectProtein complementation assayen_US
dc.subjectProtein-protein interactionsen_US
dc.titleSimple method for studying in vitro protein-protein interactions based on protein complementation and its application in drug screening targeting bacterial transcriptionen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage521-
dc.identifier.epage527-
dc.identifier.volume5-
dc.identifier.issue4-
dc.identifier.doi10.1021/acsinfecdis.9b00020-
dcterms.abstractProtein-protein interactions (PPIs) underpin essential cellular processes of all organisms and are increasingly considered as drug targets. A number of techniques have been established to study PPIs; however, development of a simple and cost-effective method for in vitro high throughput screening of PPI inhibitors is still in demand or desirable. We report herein a simple method based on protein complementation for the in vitro study of PPIs, as well as screening of inhibitors against the PPI of interest. We have validated this system utilizing bacterial transcription factors NusB and NusE. Three derivatives of an inhibitor targeting the NusB-NusE interaction were synthesized and characterized with the system, which showed specific inhibition and antimicrobial activities. We have further confirmed the system with the RNA polymeraseâ'σ interaction and an inhibitor. This system is expected to be suitable for more extensive high throughput screening of large chemical libraries. Additionally, our vector system can be easily adapted to study other PPI pairs, followed by inhibitor screening for hit identification in the application of early stage drug discovery.-
dcterms.accessRightsopen access-
dcterms.bibliographicCitationACS infectious diseases, 12 Apr. 2019, v. 5, no. 4, p. 521-527-
dcterms.isPartOfACS infectious diseases-
dcterms.issued2019-04-12-
dc.identifier.scopus2-s2.0-85062817101-
dc.identifier.pmid30834747-
dc.identifier.eissn2373-8227-
dc.description.validate202105 bcvc-
dc.description.oaAccepted Manuscript-
dc.identifier.FolderNumbera0734-n02-
dc.identifier.SubFormID1301-
dc.description.fundingSourceRGC-
dc.description.fundingSourceOthers-
dc.description.fundingTextRGC: 25100017-
dc.description.fundingTextOthers: P0020297, P0000161-
dc.description.pubStatusPublished-
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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