Publication:
Phosphocreatine interacts with phospholipids, affects membrane properties and exerts membrane-protective effects

cris.virtual.author-orcid0000-0003-3378-8765
cris.virtualsource.author-orcid3bbfaeaf-45ab-4e34-a05b-014e70c97e48
datacite.rightsopen.access
dc.contributor.authorTokarska-Schlattner, Malgorzata
dc.contributor.authorEpand, Raquel F.
dc.contributor.authorMeiler, Flurina
dc.contributor.authorZandomeneghi, Giorgia
dc.contributor.authorNeumann, Dietbert
dc.contributor.authorWidmer, Hans Rudolf
dc.contributor.authorMeier, Beat H.
dc.contributor.authorEpand, Richard M.
dc.contributor.authorSaks, Valdur
dc.contributor.authorWallimann, Theo
dc.contributor.authorSchlattner, Uwe
dc.date.accessioned2024-10-11T13:39:57Z
dc.date.available2024-10-11T13:39:57Z
dc.date.issued2012
dc.description.abstractA broad spectrum of beneficial effects has been ascribed to creatine (Cr), phosphocreatine (PCr) and their cyclic analogues cyclo-(cCr) and phospho-cyclocreatine (PcCr). Cr is widely used as nutritional supplement in sports and increasingly also as adjuvant treatment for pathologies such as myopathies and a plethora of neurodegenerative diseases. Additionally, Cr and its cyclic analogues have been proposed for anti-cancer treatment. The mechanisms involved in these pleiotropic effects are still controversial and far from being understood. The reversible conversion of Cr and ATP into PCr and ADP by creatine kinase, generating highly diffusible PCr energy reserves, is certainly an important element. However, some protective effects of Cr and analogues cannot be satisfactorily explained solely by effects on the cellular energy state. Here we used mainly liposome model systems to provide evidence for interaction of PCr and PcCr with different zwitterionic phospholipids by applying four independent, complementary biochemical and biophysical assays: (i) chemical binding assay, (ii) surface plasmon resonance spectroscopy (SPR), (iii) solid-state (31)P-NMR, and (iv) differential scanning calorimetry (DSC). SPR revealed low affinity PCr/phospholipid interaction that additionally induced changes in liposome shape as indicated by NMR and SPR. Additionally, DSC revealed evidence for membrane packing effects by PCr, as seen by altered lipid phase transition. Finally, PCr efficiently protected against membrane permeabilization in two different model systems: liposome-permeabilization by the membrane-active peptide melittin, and erythrocyte hemolysis by the oxidative drug doxorubicin, hypoosmotic stress or the mild detergent saponin. These findings suggest a new molecular basis for non-energy related functions of PCr and its cyclic analogue. PCr/phospholipid interaction and alteration of membrane structure may not only protect cellular membranes against various insults, but could have more general implications for many physiological membrane-related functions that are relevant for health and disease.
dc.description.numberOfPages1
dc.description.sponsorshipUniversitätsklinik für Neurochirurgie
dc.identifier.doi10.7892/boris.14891
dc.identifier.isi000308063700056
dc.identifier.pmid22912820
dc.identifier.publisherDOI10.1371/journal.pone.0043178
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/84943
dc.language.isoen
dc.publisherPublic Library of Science
dc.publisher.placeLawrence, Kans.
dc.relation.ispartofPLoS ONE
dc.relation.issn1932-6203
dc.relation.organizationDCD5A442C057E17DE0405C82790C4DE2
dc.titlePhosphocreatine interacts with phospholipids, affects membrane properties and exerts membrane-protective effects
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue8
oaire.citation.startPagee43178
oaire.citation.volume7
oairecerif.author.affiliationUniversitätsklinik für Neurochirurgie
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unibe.description.ispublishedpub
unibe.eprints.legacyId14891
unibe.journal.abbrevTitlePLOS ONE
unibe.refereedtrue
unibe.subtype.articlejournal

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