Publication:
Attenuation of Type IV pili activity by natural products

dc.contributor.coauthorYalkut, Kerem
dc.contributor.coauthorHassine, Soumaya Ben Ali
dc.contributor.coauthorKula, Ceyda
dc.contributor.coauthorOzcan, Aslihan
dc.contributor.coauthorAvci, Fatma Gizem
dc.contributor.coauthorAkbulut, Berna Sariyar
dc.contributor.coauthorOzbek, Pemra
dc.contributor.departmentDepartment of Chemical and Biological Engineering
dc.contributor.kuauthorBaşaran, Esra
dc.contributor.kuauthorKeskin, Özlem
dc.contributor.otherDepartment of Chemical and Biological Engineering
dc.contributor.schoolcollegeinstituteGraduate School of Sciences and Engineering
dc.contributor.schoolcollegeinstituteCollege of Engineering
dc.date.accessioned2024-12-29T09:38:16Z
dc.date.issued2024
dc.description.abstractThe virulence factor Type IV pili (T4P) are surface appendages used by the opportunistic pathogen Pseudomonas aeruginosa for twitching motility and adhesion in the environment and during infection. Additionally, the use of these appendages by P. aeruginosa for biofilm formation increases its virulence and drug resistance. Therefore, attenuation of the activity of T4P would be desirable to control P. aeruginosa infections. Here, a computational approach has been pursued to screen natural products that can be used for this purpose. PilB, the elongation ATPase of the T4P machinery in P. aeruginosa, has been selected as the target subunit and virtual screening of FDA-approved drugs has been conducted. Screening identified two natural compounds, ergoloid and irinotecan, as potential candidates for inhibiting this T4P-associated ATPase in P. aeruginosa. These candidate compounds underwent further rigorous evaluation through molecular dynamics (MD) simulations and then through in vitro twitching motility and biofilm inhibition assays. Notably, ergoloid emerged as a particularly promising candidate for weakening the T4P activity by inhibiting the elongation ATPases associated with T4P. This repurposing study paves the way for the timely discovery of antivirulence drugs as an alternative to classical antibiotic treatments to help combat infections caused by P. aeruginosa and related pathogens.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuTÜBİTAK
dc.description.sponsorsSupport from TUBITAK 120M225 is kindly acknowledged. AO acknowledges YOK 100/2000. EB acknowledges BIDEB 2211-A. KY acknowledges BIDEB 2209-A and 2247-C.
dc.identifier.doi10.1080/07391102.2024.2310781
dc.identifier.eissn1538-0254
dc.identifier.issn0739-1102
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85184205859
dc.identifier.urihttps://doi.org/10.1080/07391102.2024.2310781
dc.identifier.urihttps://hdl.handle.net/20.500.14288/22637
dc.identifier.wos1156528900001
dc.keywordsAntivirulence
dc.keywordsDrug discovery
dc.keywordsMolecular docking
dc.keywordsMolecular dynamics simulations
dc.keywordsPilB
dc.keywordsType IV pili
dc.keywordsVirtual library screening
dc.keywordsTwitching motility
dc.keywordsBiofilm inhibition
dc.languageen
dc.publisherTaylor & Francis Inc
dc.relation.grantnoTUBITAK [120M225]
dc.relation.grantnoYOK [100/2000, BIDEB 2211-A, BIDEB 2209-A, 2247-C]
dc.sourceJournal of Biomolecular Structure and Dynamics
dc.subjectBiochemistry and molecular biology
dc.subjectBiophysics
dc.titleAttenuation of Type IV pili activity by natural products
dc.typeJournal article
dspace.entity.typePublication
local.contributor.kuauthorBaşaran, Esra
local.contributor.kuauthorKeskin, Özlem
relation.isOrgUnitOfPublicationc747a256-6e0c-4969-b1bf-3b9f2f674289
relation.isOrgUnitOfPublication.latestForDiscoveryc747a256-6e0c-4969-b1bf-3b9f2f674289

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