Antimicrobial activity of an abiotic host defense peptide mimic.

[1]  G. Tew,et al.  Observing a molecular knife at work. , 2006, Journal of the American Chemical Society.

[2]  G. Tew,et al.  Membrane activity of biomimetic facially amphiphilic antibiotics. , 2006, The journal of physical chemistry. B.

[3]  M. B. Banaszak Holl,et al.  Membrane thinning due to antimicrobial peptide binding: an atomic force microscopy study of MSI-78 in lipid bilayers. , 2005, Biophysical journal.

[4]  B. Orr,et al.  Synthetic and natural polycationic polymer nanoparticles interact selectively with fluid-phase domains of DMPC lipid bilayers. , 2005, Langmuir : the ACS journal of surfaces and colloids.

[5]  A. Ramamoorthy,et al.  Antimicrobial activity and membrane selective interactions of a synthetic lipopeptide MSI-843. , 2005, Biochimica et biophysica acta.

[6]  Robert E W Hancock,et al.  Rational Design of α-Helical Antimicrobial Peptides with Enhanced Activities and Specificity/Therapeutic Index* , 2005, Journal of Biological Chemistry.

[7]  R. J. Doerksen,et al.  Synthesis of urea oligomers and their antibacterial activity. , 2005, Chemical communications.

[8]  W. DeGrado,et al.  Amphiphilic polymethacrylate derivatives as antimicrobial agents. , 2005, Journal of the American Chemical Society.

[9]  G. Tew,et al.  Tuning the hemolytic and antibacterial activities of amphiphilic polynorbornene derivatives. , 2004, Journal of the American Chemical Society.

[10]  G. Tew,et al.  Nonhemolytic abiogenic polymers as antimicrobial peptide mimics , 2004 .

[11]  S. Gellman,et al.  Antimicrobial 14-Helical β-Peptides: Potent Bilayer Disrupting Agents† , 2004 .

[12]  H. Won,et al.  Systematic Peptide Engineering and Structural Characterization to Search for the Shortest Antimicrobial Peptide Analogue of Gaegurin 5* , 2004, Journal of Biological Chemistry.

[13]  R. J. Doerksen,et al.  Nontoxic membrane-active antimicrobial arylamide oligomers. , 2004, Angewandte Chemie.

[14]  D. M. Lynn,et al.  Biocidal activity of polystyrenes that are cationic by virtue of protonation. , 2004, Organic letters.

[15]  A. Barron,et al.  Helical peptoid mimics of magainin-2 amide. , 2003, Journal of the American Chemical Society.

[16]  H. Lencastre,et al.  Evolution of Sporadic Isolates of Methicillin-Resistant Staphylococcus aureus (MRSA) in Hospitals and Their Similarities to Isolates of Community-Acquired MRSA , 2003 .

[17]  A. Ramamoorthy,et al.  MSI-78, an analogue of the magainin antimicrobial peptides, disrupts lipid bilayer structure via positive curvature strain. , 2003, Biophysical journal.

[18]  G. Tew,et al.  Cationic Facially Amphiphilic Poly(phenylene ethynylene)s Studied at the Air−Water Interface , 2003 .

[19]  G. Tew,et al.  New poly(phenyleneethynylene)s with cationic, facially amphiphilic structures. , 2002, Journal of the American Chemical Society.

[20]  R. J. Doerksen,et al.  De novo design of biomimetic antimicrobial polymers , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[21]  M. Zasloff.  Antimicrobial peptides of multicellular organisms , 2002, Nature.

[22]  W. DeGrado,et al.  De Novo Design, Synthesis, and Characterization of Antimicrobial β-Peptides , 2001 .

[23]  S. Gellman,et al.  Antibiotics: Non-haemolytic β-amino-acid oligomers , 2000, Nature.

[24]  B. Murray,et al.  Vancomycin-resistant enterococcal infections. , 2000, The New England journal of medicine.

[25]  J. Porter.  Patent confusion in law on new plant varieties , 2000, Nature.

[26]  H. G. Boman.  Innate immunity and the normal microflora , 2000, Immunological reviews.

[27]  W. DeGrado,et al.  De Novo Design of Antibacterial β-Peptides , 1999 .

[28]  R. Hancock,et al.  Cationic peptides: a new source of antibiotics. , 1998, Trends in biotechnology.

[29]  P. Moreillon,et al.  Levofloxacin versus ciprofloxacin, flucloxacillin, or vancomycin for treatment of experimental endocarditis due to methicillin-susceptible or -resistant Staphylococcus aureus , 1997, Antimicrobial agents and chemotherapy.

[30]  M. Dathe,et al.  Hydrophobicity, hydrophobic moment and angle subtended by charged residues modulate antibacterial and haemolytic activity of amphipathic helical peptides , 1997, FEBS letters.

[31]  A. Tomasz,et al.  Multiple-antibiotic-resistant pathogenic bacteria. A report on the Rockefeller University Workshop. , 1994, The New England journal of medicine.

[32]  M. Zasloff,et al.  Magainins, a class of antimicrobial peptides from Xenopus skin: isolation, characterization of two active forms, and partial cDNA sequence of a precursor , 1987 .

[33]  Darin L. Lee,et al.  Structure–activity relationships of de novo designed cyclic antimicrobial peptides based on gramicidin S , 2003, Biopolymers.

[34]  Y. Shai,et al.  Mode of action of membrane active antimicrobial peptides. , 2002, Biopolymers.

[35]  W. Maloy,et al.  Structure–activity studies on magainins and other host defense peptides , 1995, Biopolymers.