Abstract
Two new analogs of aurein 1.2 antimicrobial peptide were synthesized and the antimicrobial activities were investigated. The results showed that the activity of G1R/F3W analog was higher than the native peptide and the F3W analog. Circular dichroism studies also showed that the secondary structure of the F3W was concentration-dependent, whereas, there was no such relationship seen in the case of G1R/F3W analog. It has been proposed that G1R/F3W activity was based on a single mechanism (snorkeling), while Aurein 1.2 and F3W utilized the snorkeling mechanism at low concentrations (0-0.01 mM) and the carpet mechanism at higher concentrations (0.01-0.1 mM). This study suggests that one pay attention to the concentration of biomolecules in peptide-based drug design. © 2011 Asian Network for Scientific Information.
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Soufian, S., & Hassani, L. (2011). Study of structure-activity relationship in aurein 1.2 analogs. Pakistan Journal of Biological Sciences, 14(14), 729–735. https://doi.org/10.3923/pjbs.2011.729.735
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