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@ARTICLE{Kamiski:191812,
      author       = {Kamiński, Daniel M. and Czernel, Grzegorz and Murphy,
                      Bridget and Runge, Benjamin and Magnussen, Olaf M. and
                      Gagoś, Mariusz},
      title        = {{E}ffect of cholesterol and ergosterol on the antibiotic
                      amphotericin {B} interactions with
                      dipalmitoylphosphatidylcholine monolayers: {X}-ray
                      reflectivity study},
      journal      = {Biochimica et biophysica acta / Biomembranes},
      volume       = {1838},
      number       = {11},
      issn         = {0005-2736},
      address      = {Amsterdam},
      publisher    = {Elsevier},
      reportid     = {PUBDB-2014-04000},
      pages        = {2947 - 2953},
      year         = {2014},
      abstract     = {Amphotericin B is a Streptomyces nodosus metabolite and one
                      of the oldest polyene antibiotics used in the treatment of
                      invasive systemic fungal infections. Despite its over
                      50-year existence in clinical practice and the recognition
                      of amphotericin B as the gold standard in the treatment of
                      serious systemic mycosis, it still remains one of the most
                      toxic pharmaceuticals. Understanding of the processes at the
                      molecular levels and the interactions between amphotericin B
                      with lipid membranes containing sterols should elucidate the
                      mechanisms of the action and toxicity of this widely used
                      antibiotic. In this work, we use X-ray reflectivity to study
                      the structural changes on a molecular scale after
                      amphotericin B incorporation. These changes are accompanied
                      by an increase in monolayer surface pressure which is more
                      pronounced for ergosterol — rather than cholesterol-rich
                      membranes. The data indicate that this difference is not due
                      to the higher affinity of amphotericin B towards
                      ergosterol-containing membranes but is rather due to a ~ 3
                      Angstrom corrugation of the monolayer. Furthermore, the
                      total quantity of amphotericin B incorporated into lipid
                      monolayers containing cholesterol and ergosterol is the
                      same.},
      cin          = {DOOR},
      ddc          = {570},
      cid          = {I:(DE-H253)HAS-User-20120731},
      pnm          = {PETRA Beamline P08 (POF2-54G14)},
      pid          = {G:(DE-H253)POF2-P08-20130405},
      experiment   = {EXP:(DE-H253)P-P08-20150101},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:000342477400020},
      pubmed       = {pmid:25128151},
      doi          = {10.1016/j.bbamem.2014.08.004},
      url          = {https://bib-pubdb1.desy.de/record/191812},
}