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dc.date.accessioned2020-07-14T17:55:04Z
dc.date.available2020-07-14T17:55:04Z
dc.date.created2020-03-31T13:35:06Z
dc.date.issued2020
dc.identifier.citationJakubec, Martin Totland, Christian Rise, Frode Chamgordani, Elahe Jafari Paulsen, Britt Maes, Louis Matheeussen, An Gundersen, Lise-Lotte Halskau, Øyvind . Bioactive Metabolites of Marine Origin Have Unusual Effects on Model Membrane Systems. Marine Drugs. 2020, 18(2)
dc.identifier.urihttp://hdl.handle.net/10852/77889
dc.description.abstractMarine sponges and soft corals have yielded novel compounds with antineoplastic and antimicrobial activities. Their mechanisms of action are poorly understood, and in most cases, little relevant experimental evidence is available on this topic. In the present study, we investigated whether agelasine D (compound 1) and three agelasine analogs (compound 2–4) as well as malonganenone J (compound 5), affect the physical properties of a simple lipid model system, consisting of dioleoylphospahtidylcholine and dioleoylphosphatidylethanolamine. The data indicated that all the tested compounds increased stored curvature elastic stress, and therefore, tend to deform the bilayer which occurs without a reduction in the packing stress of the hexagonal phase. Furthermore, lower concentrations (1%) appear to have a more pronounced effect than higher ones (5–10%). For compounds 4 and 5, this effect is also reflected in phospholipid headgroup mobility assessed using 31P chemical shift anisotropy (CSA) values of the lamellar phases. Among the compounds tested, compound 4 stands out with respect to its effects on the membrane model systems, which matches its efficacy against a broad spectrum of pathogens. Future work that aims to increase the pharmacological usefulness of these compounds could benefit from taking into account the compound effects on the fluid lamellar phase at low concentrations
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleBioactive Metabolites of Marine Origin Have Unusual Effects on Model Membrane Systems
dc.typeJournal article
dc.creator.authorJakubec, Martin
dc.creator.authorTotland, Christian
dc.creator.authorRise, Frode
dc.creator.authorChamgordani, Elahe Jafari
dc.creator.authorPaulsen, Britt
dc.creator.authorMaes, Louis
dc.creator.authorMatheeussen, An
dc.creator.authorGundersen, Lise-Lotte
dc.creator.authorHalskau, Øyvind
cristin.unitcode185,15,12,57
cristin.unitnameOrganisk kjemi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1804567
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Marine Drugs&rft.volume=18&rft.spage=&rft.date=2020
dc.identifier.jtitleMarine Drugs
dc.identifier.volume18
dc.identifier.issue2
dc.identifier.doihttps://doi.org/10.3390/md18020125
dc.identifier.urnURN:NBN:no-80995
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1660-3397
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/77889/2/Jakubec_Totland_etal%25282020%2529.pdf
dc.type.versionPublishedVersion
cristin.articleid125
dc.relation.projectNFR/240063
dc.relation.projectNFR/209330


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