Poly-l-lysines and poly-l-arginines induce leakage of negatively charged phospholipid vesicles and translocate through the lipid bilayer upon electrostatic binding to the membrane

Biophysical Chemistry

Volumn 144, Issue 1-2, 2009, Pages 27-37

  Reuter, Marcel ^a   Schwieger, Christian ^a   Meister, Annette ^a   Karlsson, Göran ^b   Blume, Alfred ^a  

^a MARTIN LUTHER UNIVERSITY HALLE WITTENBERG   (Germany)

^b UPPSALA UNIVERSITY   (Sweden)

Author keywords

Cationic polypeptides; Dye release assay; Peptide lipid interactions; Phospholipid membranes

Indexed keywords

1 PALMITOYL 2 OLEOYL SN GLYCERO 3 PHOSPHOGLYCEROL; 1,2 DIPALMITOYL OLEOYL SN GLYCERO 3 PHOSPHOGLYCEROL; GLYCEROL; PHOSPHOLIPID; POLYARGININE; POLYLYSINE; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; ELECTRICITY; FLUORESCENCE ANALYSIS; ISOTHERMAL TITRATION CALORIMETRY; LIPID BILAYER; MEMBRANE BINDING; MEMBRANE PERMEABILITY; MEMBRANE STRUCTURE; MEMBRANE TRANSPORT; PHOSPHOLIPID TRANSFER; PHOSPHOLIPID VESICLE; PRIORITY JOURNAL; PROTEIN INTERACTION;

CRYOELECTRON MICROSCOPY; FLUORESCENT DYES; LIPID BILAYERS; LIPOSOMES; MEMBRANES, ARTIFICIAL; PEPTIDES; PHOSPHATIDYLGLYCEROLS; POLYLYSINE; STATIC ELECTRICITY;

EID: 67849090376     PISSN: 03014622     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bpc.2009.06.002     Document Type: Article

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