Targeting PCNA with peptide mimetics for therapeutic purposes

dc.contributor.authorHorsfall, A.J.
dc.contributor.authorAbell, A.D.
dc.contributor.authorBruning, J.
dc.date.issued2020
dc.description.abstractProliferating cell nuclear antigen (PCNA) is an excellent inhibition target to shut down highly proliferative cells and thereby develop a broad‐spectrum cancer therapeutic. It interacts with a wide variety of proteins through a conserved motif referred to as the PCNA‐interacting protein (PIP) box. There is large sequence diversity between high‐affinity PCNA binding partners, but with conservation of the binding structure - a well‐defined 3₁₀‐helix. Herein, all current PIP‐box peptides crystallised with human PCNA are collated to reveal common trends between binding structure and affinity. Key intra‐ and intermolecular hydrogen‐bonding networks that stabilise the 3₁₀‐helix of PIP‐box partners are highlighted and related back to the canonical PIP‐box motif. High correlation with the canonical PIP‐box sequence does not directly afford high affinity. Instead, we summarise key interactions that stabilise the binding structure that leads to enhanced PCNA binding affinity. These interactions also implicate the “non‐conserved” residues within the PIP‐box that have previously been overlooked. Such insights will allow a more directed approach to develop therapeutic PCNA inhibitors.
dc.description.statementofresponsibilityAimee J. Horsfall, Andrew D. Abell and John B. Bruning
dc.identifier.citationChemBioChem: a European journal of chemical biology, 2020; 21(4):442-450
dc.identifier.doi10.1002/cbic.201900275
dc.identifier.issn1439-7633
dc.identifier.issn1439-7633
dc.identifier.orcidHorsfall, A.J. [0000-0003-1276-2742]
dc.identifier.orcidAbell, A.D. [0000-0002-0604-2629]
dc.identifier.orcidBruning, J. [0000-0002-6919-1824]
dc.identifier.urihttp://hdl.handle.net/2440/123757
dc.language.isoen
dc.publisherWiley
dc.relation.granthttp://purl.org/au-research/grants/arc/CE140100003
dc.rights© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
dc.source.urihttps://doi.org/10.1002/cbic.201900275
dc.subjectPCNA; peptide mimetics
dc.titleTargeting PCNA with peptide mimetics for therapeutic purposes
dc.typeJournal article
pubs.publication-statusPublished

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