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The NK-lysin derived peptide NK-2 preferentially kills cancer cells with increased surface levels of negatively charged phosphatidylserine
Authors:Schröder-Borm Hannah  Bakalova Rumiana  Andrä Jörg
Affiliation:Department of Biochemistry and Molecular Biology, University of Hamburg, D-20146 Hamburg, Germany.
Abstract:The NK-lysin derived peptide NK-2 is a potent antibacterial, but non-toxic to a human keratinocyte cell line and of low hemolytic activity. Its target selectivity is based upon a strong binding preference to membranes containing anionic phospholipids, which are normally not found on the surface of human cells. Here, we analyzed the interaction of NK-2 with normal human lymphocytes and seven different human cancer cell lines and demonstrate that some of these cells expose negatively charged surface phosphatidylserine (PS), which presumably facilitates killing of the cells by NK-2. This is underlined by the specific intercalation of the peptide into PS-containing liposomes analyzed by fluorescence-resonance energy transfer spectroscopy.
Keywords:FACS, Fluorescence-activated cell sorter   FRET, fluorescence-resonance energy transfer spectroscopy   NB, neuroblastoma   PC, phosphatidylcholine   PE, phosphatidylethanolamine   PS, phosphatidylserine   PI, propidium iodide
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