{Reference Type}: Journal Article
{Title}: Capping motifs in antimicrobial peptides and their relevance for improved biological activities.
{Author}: Brango-Vanegas J;Leite ML;Macedo MLR;Cardoso MH;Franco OL;
{Journal}: Front Chem
{Volume}: 12
{Issue}: 0
{Year}: 2024
{Factor}: 5.545
{DOI}: 10.3389/fchem.2024.1382954
{Abstract}: N-capping (N-cap) and C-capping (C-cap) in biologically active peptides, including specific amino acids or unconventional group motifs, have been shown to modulate activity against pharmacological targets by interfering with the peptide's secondary structure, thus generating unusual scaffolds. The insertion of capping motifs in linear peptides has been shown to prevent peptide degradation by reducing its susceptibility to proteolytic cleavage, and the replacement of some functional groups by unusual groups in N- or C-capping regions in linear peptides has led to optimized peptide variants with improved secondary structure and enhanced activity. Furthermore, some essential amino acid residues that, when placed in antimicrobial peptide (AMP) capping regions, are capable of complexing metals such as Cu2+, Ni2+, and Zn2+, give rise to the family known as metallo-AMPs, which are capable of boosting antimicrobial efficacy, as well as other activities. Therefore, this review presents and discusses the different strategies for creating N- and C-cap motifs in AMPs, aiming at fine-tuning this class of antimicrobials.