Improving the Therapeutic Index of Smp24, a Venom-Derived Antimicrobial Peptide: Increased Activity against Gram-Negative Bacteria.
Kirstie M Rawson, Melissa M Lacey, Peter N Strong, Keith Miller
Author Information
Kirstie M Rawson: Biomolecular Sciences Research Centre, Department of Biosciences and Chemistry, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, UK.
Melissa M Lacey: Biomolecular Sciences Research Centre, Department of Biosciences and Chemistry, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, UK.
Peter N Strong: Biomolecular Sciences Research Centre, Department of Biosciences and Chemistry, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, UK.
Keith Miller: Biomolecular Sciences Research Centre, Department of Biosciences and Chemistry, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, UK. ORCID
Antimicrobial peptides (AMPs) are naturally occurring compounds which possess a rapid killing mechanism and low resistance potential. Consequently, they are being viewed as potential alternatives to traditional antibiotics. One of the major factors limiting further development of AMPs is off-target toxicity. Enhancements to antimicrobial peptides which can maximise antimicrobial activity whilst reducing mammaliancytotoxicity would make these peptides more attractive as future pharmaceuticals. We have previously characterised Smp24, an AMP derived from the venom of the scorpion . This study sought to better understand the relationship between the structure, function and bacterial selectivity of this peptide by performing single amino acid substitutions. The antimicrobial, haemolytic and cytotoxic activity of modified Smp24 peptides was determined. The results of these investigations were compared with the activity of native Smp24 to determine which modifications produced enhanced therapeutic indices. The structure-function relationship of Smp24 was investigated by performing N-terminal, mid-chain and C-terminal amino acid substitutions and determining the effect that they had on the antimicrobial and cytotoxic activity of the peptide. Increased charge at the N-, mid- and C-termini of the peptide resulted in increased antimicrobial activity. Increased hydrophobicity at the N-terminus resulted in reduced haemolysis and cytotoxicity. Reduced antimicrobial, haemolytic and cytotoxic activity was observed by increased hydrophobicity at the mid-chain. Functional improvements have been made to modified peptides when compared with native Smp24, which has produced peptides with enhanced therapeutic indices.
