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Antimicrobial Agents and Chemotherapy, July 1999, p. 1704-1707, Vol. 43, No. 7
Protein Chemistry Laboratory, Mogam
Biotechnology Research Institute, Kyunggi-Do, 449-910, Korea
Received 7 December 1998/Returned for modification 27 January
1999/Accepted 23 April 1999
In the present study, we investigated the antifungal activity and
cytotoxicity of a novel membrane-active peptide, KKVVFKVKFKK (MP). MP inhibited the growth of various pathogenic fungi
isolated from patients and of fluconazole-resistant fungi at
concentrations of 2 to 32 µg/ml. MP had potent fungicidal activity;
the minimal fungicidal concentrations of the peptide were no more than
fourfold greater than the MICs. Time course experiments of MP-induced
killing of Candida albicans ATCC 36232 showed that the rate
of killing was rapid and depended on the concentration of MP. MP had a
strong synergism with other antifungal drugs; the fractional inhibitory concentration index values of MP with amphotericin B and fluconazole for C. albicans were 0.16 and 0.02, respectively. The 50%
inhibitory concentrations of MP for NIH 3T3 and Jurkat cells were
approximately 100 times higher than the MIC for C. albicans
ATCC 36232, indicating that MP had high selectivity between the fungal
and mammalian cells. These results suggest that MP has great advantages
in the development of antifungal agents.
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
In Vitro Antifungal Activity and Cytotoxicity of a
Novel Membrane-Active Peptide
*
Corresponding author. Mailing address: Protein
Chemistry Laboratory, Mogam Biotechnology Research Institute, 341 Pojung-Ri, Koosung-Myun, Youngin City, Kyunggi-Do, 449-910, Korea.
Phone: 82-331-262-3851. Fax: 82-331-262-6622. E-mail:
lkh{at}kgcc.co.kr.
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