Show simple item record

dc.contributor.authorJiang, Jingboen
dc.contributor.authorHoagland, Daniel T.en
dc.contributor.authorPalatinus, Joseph A.en
dc.contributor.authorHe, Huameien
dc.contributor.authorIyyathurai, Jeganen
dc.contributor.authorJourdan, L. Janeen
dc.contributor.authorBultynck, Geerten
dc.contributor.authorWang, Zhenen
dc.contributor.authorZhang, Zhiweien
dc.contributor.authorSchey, Kevinen
dc.contributor.authorPoelzing, Stevenen
dc.contributor.authorMcGowan, Francis X.en
dc.contributor.authorGourdie, Robert G.en
dc.date.accessioned2019-08-20T12:25:57Zen
dc.date.available2019-08-20T12:25:57Zen
dc.date.issued2019-08-19en
dc.identifier.urihttp://hdl.handle.net/10919/93188en
dc.description.abstractBackground α Carboxyl terminus 1 (αCT1) is a 25–amino acid therapeutic peptide incorporating the zonula occludens‐1 (ZO‐1)–binding domain of connexin 43 (Cx43) that is currently in phase 3 clinical testing on chronic wounds. In mice, we reported that αCT1 reduced arrhythmias after cardiac injury, accompanied by increases in protein kinase Cε phosphorylation of Cx43 at serine 368. Herein, we characterize detailed molecular mode of action of αCT1 in mitigating cardiac ischemia‐reperfusion injury. Methods and Results To study αCT1‐mediated increases in phosphorylation of Cx43 at serine 368, we undertook mass spectrometry of protein kinase Cε phosphorylation assay reactants. This indicated potential interaction between negatively charged residues in the αCT1 Asp‐Asp‐Leu‐Glu‐Iso sequence and lysines (Lys345, Lys346) in an α‐helical sequence (helix 2) within the Cx43‐CT. In silico modeling provided further support for this interaction, indicating that αCT1 may interact with both Cx43 and ZO‐1. Using surface plasmon resonance, thermal shift, and phosphorylation assays, we characterized a series of αCT1 variants, identifying peptides that interacted with either ZO‐1–postsynaptic density‐95/disks large/zonula occludens‐1 2 or Cx43‐CT, but with limited or no ability to bind both molecules. Only peptides competent to interact with Cx43‐CT, but not ZO‐1–postsynaptic density‐95/disks large/zonula occludens‐1 2 alone, prompted increased pS368 phosphorylation. Moreover, in an ex vivo mouse model of ischemia‐reperfusion injury, preischemic infusion only with those peptides competent to bind Cx43 preserved ventricular function after ischemia‐reperfusion. Interestingly, a short 9–amino acid variant of αCT1 (αCT11) demonstrated potent cardioprotective effects when infused either before or after ischemic injury. Conclusions Interaction of αCT1 with the Cx43, but not ZO‐1, is correlated with cardioprotection. Pharmacophores targeting Cx43‐CT could provide a translational approach to preserving heart function after ischemic injury.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherAmerican Heart Associationen
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en
dc.subjectconnexin 43en
dc.subjectα carboxyl terminus 1en
dc.subjectS368 phosphorylationen
dc.subjectischemia‐reperfusion injuryen
dc.subjectzonula occludens‐1 cardioprotectionen
dc.subjectcardioprotectionen
dc.titleInteraction of α Carboxyl Terminus 1 Peptide With the Connexin 43 Carboxyl Terminus Preserves Left Ventricular Function After Ischemia‐Reperfusion Injuryen
dc.typeArticle - Refereeden
dc.title.serialJournal of the American Heart Associationen
dc.identifier.doihttps://doi.org/10.1161/JAHA.119.012385en
dc.identifier.volume8en
dc.identifier.issue16en
dc.type.dcmitypeTexten
dc.type.dcmitypeStillImageen


Files in this item

Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record

Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
License: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International