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Kinetic and structural analysis of redox-reversible artificial imine reductases

dc.contributor.authorMiller, Alex H.
dc.contributor.authorMartins, Ingrid B.S. [UNESP]
dc.contributor.authorBlagova, Elena V.
dc.contributor.authorWilson, Keith S.
dc.contributor.authorDuhme-Klair, Anne-K.
dc.contributor.institutionUniversity of York
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionFederal University of Rio de Janeiro
dc.date.accessioned2025-04-29T18:42:54Z
dc.date.issued2024-11-01
dc.description.abstractThree artificial imine reductases, constructed via supramolecular anchoring utilising FeIII-azotochelin, a natural siderophore, to bind an iridium-containing catalyst to periplasmic siderophore-binding protein (PBP) scaffolds, have previously been synthesised and subjected to catalytic testing. Despite exhibiting high homology and possessing conserved siderophore anchor coordinating residues, the three artificial metalloenzymes (ArMs) displayed significant variability in turnover frequencies (TOFs). To further understand the catalytic properties of these ArMs, their kinetic behaviour was evaluated with respect to the reduction of three cyclic imines: dihydroisoquinoline, harmaline, and papaverine. Kinetic analyses revealed that all examined ArMs adhere to Michaelis-Menten kinetics, with the most pronounced saturation profile observed for the substrate harmaline. Additionally, molecular docking studies suggested varied hydrogen-bonding interactions between substrates and residues within the artificial binding pocket. Pi-stacking and pi-cation interactions were identified for harmaline and papaverine, corroborating the higher affinity of these substrates for the ArMs in comparison to dihydroisoquinoline. Furthermore, it was demonstrated that multiple cavities are capable of accommodating substrates in close proximity to the catalytic centre, thereby rationalising the moderate enantioselectivity conferred by the unmodified scaffolds.en
dc.description.affiliationDepartment of Chemistry University of York, York
dc.description.affiliationDepartment of Physics Institute of Biosciences Humanities and Exact Sciences São Paulo State University (UNESP), São José do Rio Preto, SP
dc.description.affiliationBiophysics Institute Carlos Chagas Filho Federal University of Rio de Janeiro, RJ
dc.description.affiliationStructural Biology Laboratory Department of Chemistry University of York, York
dc.description.affiliationUnespDepartment of Physics Institute of Biosciences Humanities and Exact Sciences São Paulo State University (UNESP), São José do Rio Preto, SP
dc.description.sponsorshipBiotechnology and Biological Sciences Research Council
dc.description.sponsorshipEngineering and Physical Sciences Research Council
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ)
dc.identifierhttp://dx.doi.org/10.1016/j.jinorgbio.2024.112691
dc.identifier.citationJournal of Inorganic Biochemistry, v. 260.
dc.identifier.dimensionspub.1174512836
dc.identifier.doi10.1016/j.jinorgbio.2024.112691
dc.identifier.issn1873-3344
dc.identifier.issn0162-0134
dc.identifier.orcid0000-0001-8269-850X
dc.identifier.orcid0000-0002-2041-3043
dc.identifier.orcid0000-0002-3581-2194
dc.identifier.orcid0000-0001-6214-2459
dc.identifier.pmid39126757
dc.identifier.scopus2-s2.0-85200821304
dc.identifier.urihttps://hdl.handle.net/11449/299606
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofJournal of Inorganic Biochemistry
dc.rights.accessRightsAcesso abertopt
dc.rights.sourceRightsoa_all
dc.rights.sourceRightshybrid
dc.sourceScopus
dc.sourceDimensions
dc.subjectArtificial metalloenzymes
dc.subjectKinetics
dc.subjectMichaelis-Menten
dc.subjectMolecular docking
dc.titleKinetic and structural analysis of redox-reversible artificial imine reductasesen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication43c38943-bd6f-4fb6-a9a5-8482a1f632c0
relation.isOrgUnitOfPublication.latestForDiscovery43c38943-bd6f-4fb6-a9a5-8482a1f632c0
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Letras e Ciências Exatas, São José do Rio Pretopt

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