Quantitative interactions between cryptdin-4 amino terminal variants and membranes

Peptides

Volumn 24, Issue 11, 2003, Pages 1795-1805

  Satchell, Donald P ^a,d   Sheynis, Tanya ^b   Kolusheva, Sofiya ^b   Cummings, Jason ^c   Vanderlick, T Kyle ^c   Jelinek, Raz ^b   Selsted, Michael E ^a   Ouellette, Andre J ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b BEN GURION UNIVERSITY OF THE NEGEV   (Israel)

^c Princeton University   (United States)

^d Dow Chemical Company   (United States)

Author keywords

Innate immunity; Matrix assisted laser desorption time of flight mass spectrometry; Paneth cells; Polymerase chain reaction; Recombinant peptide expression; Reverse phase high performance liquid chromatography; Surface plasmon resonance; Defensin

Indexed keywords

AMINO ACID DERIVATIVE; ANTIINFECTIVE AGENT; ARGININE; ASPARTIC ACID; CRYPTDIN 4; GLYCINE; MEMBRANE PHOSPHOLIPID; PEPTIDE DERIVATIVE; RECOMBINANT PROTEIN; UNCLASSIFIED DRUG; VALINE;

AMINO ACID SUBSTITUTION; AMINO TERMINAL SEQUENCE; ARTICLE; BACTERICIDAL ACTIVITY; BINDING AFFINITY; CELL MEMBRANE; CORRELATION ANALYSIS; DRUG BINDING; DRUG PENETRATION; DRUG PURIFICATION; DRUG STRUCTURE; ESCHERICHIA COLI; LIPID VESICLE; MOLECULAR INTERACTION; NONHUMAN; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS;

ESCHERICHIA COLI;

EID: 1042267411     PISSN: 01969781     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.peptides.2003.08.020     Document Type: Article

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