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Phosphatidic acid plays a special role in stabilizing and folding of the tetrameric potassium channel KcsA
Authors:Raja Mobeen  Spelbrink Robin E J  de Kruijff Ben  Killian J Antoinette
Institution:Research Group Biochemistry of Membranes, Institute of Biomembranes, Utrecht University, Padualaan 8, 3584 CH, Utrecht, The Netherlands. mobeen.raja@jku.at
Abstract:In this study, we investigated how the presence of anionic lipids influenced the stability and folding properties of the potassium channel KcsA. By using a combination of gel electrophoresis, tryptophan fluorescence and acrylamide quenching experiments, we found that the presence of the anionic lipid phosphatidylglycerol (PG) in a phosphatidylcholine (PC) bilayer slightly stabilized the tetramer and protected it from trifluoroethanol-induced dissociation. Surprisingly, the presence of phosphatidic acid (PA) had a much larger effect on the stability of KcsA and this lipid, in addition, significantly influenced the folding properties of the protein. The data indicate that PA creates some specificity over PG, and that it most likely stabilizes the tetramer via both electrostatic and hydrogen bond interactions.
Keywords:SDS-PAGE  sodium dodecylsulphate-polyacrylamide gel electrophoresis  CF  carboxyfluorescein  Trp  tryptophan
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