Tuning the membrane selectivity of antimicrobial peptides by using multivalent design

ChemBioChem

Volumn 8, Issue 17, 2007, Pages 2063-2065

  Liu, Zhigang ^a   Young, Anne W ^a   Hu, Po ^a   Rice, Amanda J ^b   Zhou, Chunhui ^a   Zhang, Yingkai ^a   Kallenbach, Neville R ^a  

^a NEW YORK UNIVERSITY   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

Author keywords

Antibiotics; Dendrimers; Multivalency; Peptides

Indexed keywords

LIPID; PHOSPHOLIPID; POLYPEPTIDE ANTIBIOTIC AGENT;

ANTIBACTERIAL ACTIVITY; ARTICLE; BACTERIAL OUTER MEMBRANE; CONCENTRATION RESPONSE; DRUG DESIGN; DRUG MANUFACTURE; GRAM POSITIVE BACTERIUM; HEMOLYSIS; LIPID BILAYER; MINIMUM INHIBITORY CONCENTRATION; PEPTIDE SYNTHESIS; PHOSPHOLIPID BILAYER; PRIORITY JOURNAL; SOLID;

ANTI-BACTERIAL AGENTS; CELL MEMBRANE; COMPUTER SIMULATION; DRUG DESIGN; FLUORESCEINS; MODELS, MOLECULAR; MOLECULAR STRUCTURE; PEPTIDES;

EID: 36849039966     PISSN: 14394227     EISSN: 14397633     Source Type: Journal    
DOI: 10.1002/cbic.200700502     Document Type: Article

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