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dc.contributor.authorF. Dulhunty, Angelaen_US
dc.contributor.authorCengia, Louiseen_US
dc.contributor.authorYoung, Jacquien_US
dc.contributor.authorM. Pace, Suzyen_US
dc.contributor.authorJ. Harvey, Petaen_US
dc.contributor.authorD. Lamb, Grahamen_US
dc.contributor.authorChan, Yiu-Ngoken_US
dc.contributor.authorWimmer, Norberten_US
dc.contributor.authorToth, Istvanen_US
dc.contributor.authorG. Casarotto, Marcoen_US
dc.date.accessioned2017-04-24T12:30:01Z
dc.date.available2017-04-24T12:30:01Z
dc.date.issued2005en_US
dc.date.modified2009-11-11T05:25:17Z
dc.identifier.issn0007-1188en_US
dc.identifier.doi10.1038/sj.bjp.0705981en_AU
dc.identifier.urihttp://hdl.handle.net/10072/26599
dc.description.abstractOur aim was to determine whether lipoamino acid conjugation of peptides that are high-affinity activators of ryanodine receptor (RyR) channels would (a) render the peptides membrane permeable, (b) alter their structure or (a) reduce their activity. The peptides correspond to the A region of the II-III loop of the skeletal dihydropyridine receptor. 2. The lipoamino acid conjugation increased the apparent permeability of the peptide across the Caco-2 cell monolayer by up to approximately 20-fold. 3. Nuclear magnetic resonance showed that the alpha-helical structure of critical basic residues, required for optimal activation of RyRs, was retained after conjugation. 4. The conjugated peptides were more effective in enhancing resting Ca2+ release, Ca2+-induced Ca2+ release and caffeine-induced Ca2+ release from isolated sarcoplasmic reticulum (SR) than their unconjugated counterparts, and significantly enhanced caffeine-induced Ca2+ release from mechanically skinned extensor digitorum longus (EDL) fibres. 5. The effect of both conjugated and unconjugated peptides on Ca2+ release from skeletal SR was 30-fold greater than their effect on either cardiac Ca2+ release or on the Ca2+ Mg2+ ATPase. 6. A small and very low affinity effect of the peptide in slowing Ca2+ uptake by the Ca2+, Mg2+ ATPase was exacerbated by lipoamino acid conjugation in both isolated SR and in skinned EDL fibres. 7. The results show that lipoamino acid conjugation of A region peptides increases their membrane permeability without impairing their structure or efficacy in activating skeletal and cardiac RyRs.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherJohn Wiley & Sonsen_US
dc.publisher.placeUnited Kingdomen_US
dc.relation.ispartofstudentpublicationNen_AU
dc.relation.ispartofpagefrom743en_US
dc.relation.ispartofpageto754en_US
dc.relation.ispartofissue6en_US
dc.relation.ispartofjournalBritish Journal of Pharmacologyen_US
dc.relation.ispartofvolume144en_US
dc.rights.retentionYen_AU
dc.subject.fieldofresearchcode320502en_US
dc.subject.fieldofresearchcode320501en_US
dc.titleFunctional implications of modifying RyR-activating peptides for membrane permeabilityen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.date.issued2005
gro.hasfulltextNo Full Text


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