Short synthetic β-sheet forming peptide amphiphiles as broad spectrum antimicrobials with antibiofilm and endotoxin neutralizing capabilities

Advanced Functional Materials

Volumn 23, Issue 29, 2013, Pages 3682-3692

  Ong, Zhan Yuin ^a   Gao, Shu Jun ^a   Yang, Yi Yan ^a  

^a INSTITUTE OF BIOENGINEERING AND NANOTECHNOLOGY   (Singapore)

Author keywords

sheet secondary structure; antibiofilm; antimicrobial peptides (AMP); broad spectrum; drug resistance; endotoxin neutralization

Indexed keywords

ANTI-BIOFILM; ANTIMICROBIAL PEPTIDE; BROAD SPECTRUM; DRUG RESISTANCE; ENDOTOXIN NEUTRALIZATION; SECONDARY STRUCTURES;

BACTERIA; ESCHERICHIA COLI; HYDROPHOBICITY; OPTIMIZATION; PEPTIDES; YEAST;

POLYPEPTIDES;

EID: 84881120375     PISSN: 1616301X     EISSN: 16163028     Source Type: Journal    
DOI: 10.1002/adfm.201202850     Document Type: Article

References (32)

1. C. Mathers, D. M. Fat, J. Boerma, The global burden of disease: 2004 update, World Health Organization, 2008.
2. S. C. Park, Y. Park, K. S. Hahm, Int. J. Mol. Sci. 2011, 12, 5971.
3. S. L. Percival, C. Emanuel, K. F. Cutting, D. W. Williams, Int. Wound J. 2012, 9, 14.
4. C. I. Kang, S. H. Kim, W. B. Park, K. D. Lee, H. B. Kim, E. C. Kim, M. Oh, K. W. Choe, Antimicrob. Agents Chemother. 2005, 49, 760.
5. S. A. David, J. Mol. Recognit. 2001, 14, 370.
6. B. Spellberg, R. Guidos, D. Gilbert, J. Bradley, H. W. Boucher, W. M. Scheld, J. G. Bartlett, J. Edwards, Clin. Infect. Dis. 2008, 46, 155.
7. M. N. Melo, R. Ferre, M. A. R. B. Castanho, Nat. Rev. Microbiol. 2009, 7, 245.
8. G. Wang, X. Li, Z. Wang, Nucleic Acids Res. 2009, 37, D933.
9. R. E. W. Hancock, H. G. Sahl, Nat. Biotechnol. 2006, 24, 1551.
10. L. T. Nguyen, J. K. Chau, N. A. Perry, L. de Boer, S. A. J. Zaat, H. J. Vogel, PLoS One 2010, 5, e12684.
11. A. Pellegrini, R. von Fellenberg, Biochim. Biophys. Acta Protein Struct. Mol. Enzymol. 1999, 1433, 122.
12. D. Lee, J. Powers, K. Pflegerl, M. Vasil, R. Hancock, R. Hodges, J. Pept. Res. 2004, 63, 69.
13. T. Godballe, L. L. Nilsson, P. D. Petersen, H. Jenssen, Chem. Biol. Drug Des. 2011, 77, 107.
14. H. Meng, K. Kumar, J. Am. Chem. Soc. 2007, 129, 15615.
15. G. Bell, P. H. Gouyon, Microbiology 2003, 149, 1367.
16. N. Wiradharma, U. Khoe, C. A. E. Hauser, S. V. Seow, S. Zhang, Y. Y. Yang, Biomaterials 2011, 32, 2204.
17. Z. Jiang, A. I. Vasil, J. D. Hale, R. E. W. Hancock, M. L. Vasil, R. S. Hodges, Pept. Sci. 2008, 90, 369.
18. Z. Jiang, A. I. Vasil, L. Gera, M. L. Vasil, R. S. Hodges, Chem. Biol. Drug Des. 2011, 77, 225.
19. Y. Jin, J. Hammer, M. Pate, Y. Zhang, F. Zhu, E. Zmuda, J. Blazyk, Antimicrob. Agents Chemother. 2005, 49, 4957.
20. W. C. Wimley, Protein Sci. 2002, 11, 301.
21. D. L. Minor Jr., P. S. Kim, Nature 1994, 367, 660.
22. C. K. Smith, J. M. Withka, L. Regan, Biochemistry (Moscow) 1994, 33, 5510.
23. K. H. Mayo, E. Ilyina, H. Park, Protein Sci. 1996, 5, 1301.
24. P. Bulet, R. Stöcklin, L. Menin, Immunol. Rev. 2004, 198, 169.
25. M. Pasupuleti, A. Schmidtchen, M. Malmsten, Crit. Rev. Biotechnol. 2012, 32, 143.
26. Y. H. Nan, S. H. Lee, H. J. Kim, S. Y. Shin, Peptides 2010, 31, 1826.
27. A. A. Langham, H. Khandelia, Y. N. Kaznessis, Pept. Sci. 2006, 84, 219.
28. C. Ried, C. Wahl, T. Miethke, G. Wellnhofer, C. Landgraf, J. Schneider-Mergener, A. Hoess, J. Biol. Chem. 1996, 271, 28120.
29. A. P. Zavascki, L. Z. Goldani, J. Li, R. L. Nation, J. Antimicrob. Chemother. 2007, 60, 1206.
30. Neomycin and Polymyxin B Sulfates and Gramicidin Ophthalmic Solution USP; MSDS No. 034; Gary Wong: Tampa, FL, May 13, 2004.
31. Y. Rosenfeld, N. Papo, Y. Shai, J. Biol. Chem. 2006, 281, 1636.
32. L. J. Ignarro, J. M. Fukuto, J. M. Griscavage, N. E. Rogers, R. E. Byrns, Proc. Natl. Acad. Sci. USA 1993, 90, 8103.