Multivalent antimicrobial peptides as therapeutics: Design principles and structural diversities

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Abstract

This review highlights the design principles, progress and advantages attributed to the structural diversity associated with both natural and synthetic multivalentantimicrobial peptides (AMPs). Natural homo- or heterodimers of AMPs linked by intermolecular disulfide bonds existed in the animal kingdom, but the multivalency strategy has been adopted to create synthetic branched or polymeric AMPs that do not exist in nature. The multivalent strategy for the design of multivalent AMPs provides advantages to overcome the challenges faced in clinical applications of AMPs, such as: stability, efficiency, toxicity, maintenance of activity in high salt concentrations and under physiological conditions, and importantly overcoming bacterial resistance which is currently a leading health problem in the world. The multivalency strategy is valuable for moving multivalent AMPs toward clinical applications. © The Author(s) 2010.

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Liu, S. P., Zhou, L., Lakshminarayanan, R., & Beuerman, R. W. (2010). Multivalent antimicrobial peptides as therapeutics: Design principles and structural diversities. In International Journal of Peptide Research and Therapeutics (Vol. 16, pp. 199–213). https://doi.org/10.1007/s10989-010-9230-z

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