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http://dx.doi.org/10.5012/bkcs.2014.35.12.3632

De Novo Design and Their Antimicrobial Activity of Stapled Amphipathic Helices of Heptapeptides  

Dinh, Thuy T.T. (College of Pharmacy, Dongguk University)
Kim, Do-Hee (College of Pharmacy, Seoul National University)
Lee, Bong-Jin (College of Pharmacy, Seoul National University)
Kim, Young-Woo (College of Pharmacy, Dongguk University)
Publication Information
Abstract
In this study we designed and synthesized several heptapeptides that are enforced to form an amphipathic helix using all-hydrocarbon stapling system and evaluated their antimicrobial and hemolytic activities. The antimicrobial activity showed clear structure-activity relationships, confirming the importance of helicity and amphipathicity. Some stapled heptapeptides displayed a moderate antimicrobial activity along with a low hemolytic activity. To our best knowledge, although not highly potent, these stapled peptides represent the shortest helical amphipathic antimicrobial peptides reported to date. The preliminary data obtained in this work would serve as a good starting point for further developing short analogs of amphipathic helical antimicrobial peptides.
Keywords
Antimicrobial peptides; ${\alpha}$-Helix; Stapled peptides; Protease resistance; Peptide drugs;
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1 Park, J. M.; Jung, J.-E.; Lee, B. J. Biochem. Biophys. Res. Commun. 1994, 205, 948-954.   DOI   ScienceOn
2 Won, H.-S.; Park, S.-H.; Kim, H. E.; Hyun, B.; Kim, M.; Lee, B. J.; Lee, B.-J. Eur. J. Biochem. 2002, 269, 4367-4374.   DOI   ScienceOn
3 Kim, Y.-W.; Grossmann, T. N.; Verdine, G. L. Nat. Proc. 2011, 6, 761-771.   DOI   ScienceOn
4 Chapuis, H.; Slaninova, J.; Bednarova, L.; Monincova, L.; Budesinsky, M.; Cerovsky, V. Amino Acids 2012, 43, 2047-2058.   DOI   ScienceOn
5 Kim, Y.-W.; Verdine, G. L. Bioorg. Med. Chem. Lett. 2009, 19, 2533-2536.   DOI   ScienceOn
6 Kim, Y.-W.; Kutchukian, P. S.; Verdine, G. L. Org. Lett. 2010, 12, 3046-3049.   DOI   ScienceOn
7 Verdine, G. L.; Hilinski, G. J. Methods Enzymol. 2012, 503, 3-33.   DOI
8 Won, H.-S.; Kang, S.-J.; Choi, W. S.; Lee, B. J. Mol. Cells 2011, 31, 49-54.   DOI   ScienceOn
9 Boman, H. G. Annu. Rev. Immunol. 1995, 13, 61-92.   DOI   ScienceOn
10 Gabay, J. E. Science 1994, 264, 373-374.   DOI
11 Yeaman, M. R.; Yount, N. Y. Pharmacol. Rev. 2003, 55, 27-55.   DOI   ScienceOn
12 Zasloff, M. Nature 2002, 415, 389-395.   DOI   ScienceOn
13 Tossi, A.; Sandri, L.; Giangaspero, A. Biopolymers 2000, 55, 4-30.   DOI   ScienceOn
14 Jenssen, H.; Hamill, P.; Hancock, R. E. W. Clin. Microbiol. Rev. 2006, 19, 491-511.   DOI   ScienceOn
15 Jiang, Z.; Vasil, A. I.; Hale, J. D.; Hancock, R. E. W.; Vasil, M. L.; Hodges, R. S. Pept. Sci. 2008, 90, 369-383.   DOI
16 Shai, Y. Biopolymers 2002, 66, 236-248.   DOI   ScienceOn
17 Huang, Y.; Huang, J.; Chen, Y. Protein Cell 2010, 1, 143-152.   DOI   ScienceOn
18 Marr, A. K.; Gooderham, W. J.; Hancock, R. E. W. Curr. Opin. Pharmacol. 2006, 6, 468-472.   DOI   ScienceOn
19 Shai, Y. Biochim. Biophys. Acta 1999, 1462, 55-70.   DOI   ScienceOn
20 Pham, T. K.; Kim, D.-H.; Lee, B.-J.; Kim, Y.-W. Bioorg. Med. Chem. Lett. 2013, 23, 6717-6720.   DOI
21 Giangaspero, A.; Sandri, L.; Tossi, A. Eur. J. Biochem. 2001, 268, 5589-600.   DOI
22 Creighton, T. E. Proteins: Structures and Molecular Properties, Freeman and Co.: New York, 1984.
23 Schafmeister, C. E.; Po, J.; Verdine, G. L. J. Am. Chem. Soc. 2000, 122, 5891-5892.   DOI   ScienceOn