Back to Search
Start Over
Design of improved synthetic antifungal peptides with targeted variations in charge, hydrophobicity and chirality based on a correlation study between biological activity and primary structure of plant defensin γ-cores.
- Source :
-
Amino acids [Amino Acids] 2021 Feb; Vol. 53 (2), pp. 219-237. Date of Electronic Publication: 2021 Jan 23. - Publication Year :
- 2021
-
Abstract
- Microbial resistance to available drugs is a growing health threat imposing the need for the development of new drugs. The scaffold of plant defensins, including their γ-cores, are particularly good candidates for drug design. This work aimed to improve the antifungal activity of a previous design peptide, named A <subscript>36</subscript> , <subscript>42</subscript> , <subscript>44</subscript> γ <subscript>32-46</subscript> VuDef (for short DD) against yeasts by altering its biochemical parameters. We explore the correlation of the biological activity and structure of plant defensins and compared their primary structures by superimposition with VuDef <subscript>1</subscript> and DD which indicated us the favorable position and the amino acid to be changed. Three new peptides with modifications in charge, hydrophobicity (RR and WR) and chirality (D-RR) were designed and tested against pathogenic yeasts. Inhibition was determined by absorbance. Viability of mammalian cells was determined by MTT. The three designed peptides had better inhibitory activity against the yeasts with better potency and spectrum of yeast species inhibition, with low toxicity to mammalian cells. WR, the most hydrophobic and cationic, exhibited better antifungal activity and lower toxicity. Our study provides experimental evidence that targeted changes in the primary structure of peptides based on plant defensins γ-core primary structures prove to be a good tool for the synthesis of new compounds that may be useful as alternative antifungal drugs. The method described did not have the drawback of synthesis of several peptides, because alterations are guided. When compared to other methods, the design process described is efficient and viable to those with scarce resources.
- Subjects :
- Amino Acid Sequence
Cell Line
Defensins chemistry
Defensins pharmacology
Drug Design
Humans
Hydrophobic and Hydrophilic Interactions
Microbial Sensitivity Tests
Yeasts drug effects
Yeasts growth & development
Antifungal Agents chemistry
Antifungal Agents pharmacology
Peptides chemistry
Peptides pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1438-2199
- Volume :
- 53
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Amino acids
- Publication Type :
- Academic Journal
- Accession number :
- 33483849
- Full Text :
- https://doi.org/10.1007/s00726-020-02929-x