Copper-binding motifs Xxx-His or Xxx-Zzz-His (ATCUN) linked to an antimicrobial peptide: Cu-binding, antimicrobial activity and ROS production

J Inorg Biochem. 2020 Dec:213:111255. doi: 10.1016/j.jinorgbio.2020.111255. Epub 2020 Sep 11.

Abstract

Depending on the coordination, copper ions can have a very high activity in catalyzing the production of reactive oxygen species. Thus interest arose in increasing the activity of antimicrobial peptides (AMPs) by equipping them with a Cu-binding unit. Several examples, native and engineered, have been investigated with the motif Xxx-Zzz-His, called Amino Terminal Cu(II)- and Ni(II)-binding (ATCUN) motif. Here we investigate a short AMP that was equipped either with Xxx-Zzz-His or Xxx-His. Xxx-His is a shorter motif and yields a more redox active copper complex. The control AMP, Xxx-His-AMP and Xxx-Zzz-His-AMP were investigated toward Cu-binding, Reactive Oxygen Species (ROS) production and antimicrobial activity in E. coli. The data indicate that these Cu-binding motifs have very limited impact on antimicrobial activity and low ROS production capability.

Keywords: Antimicrobial peptide; Copper; Metallopeptide; N-terminal Cu(II) binding site; Reactive oxygen species; Redox.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / metabolism*
  • Binding Sites
  • Copper / metabolism
  • Pore Forming Cytotoxic Proteins / metabolism*
  • Pore Forming Cytotoxic Proteins / pharmacology
  • Reactive Oxygen Species / metabolism*

Substances

  • Amino Acids
  • Pore Forming Cytotoxic Proteins
  • Reactive Oxygen Species
  • Copper