Dipicolylamine as a unique structural switching element for helical peptides

Org Biomol Chem. 2012 Aug 14;10(30):6062-8. doi: 10.1039/c2ob07118e. Epub 2012 May 22.

Abstract

Developing novel methods for metal-induced switching of peptide structures expands the design principles of functional biomolecules and biomaterials. Here, a simple method for on-resin synthesis of dipicolylamine (Dpa)-containing peptides was developed. Whereas addition of divalent metal ions such as Fe(ii) and Cu(ii) to a peptide bearing a pair of Dpa moieties at the i and i + 4 positions led to the formation of a 1:1 complex of Dpa with metals, addition of Ni(ii) yielded a cross-linked structure of Dpa-metal (2:1). This feature was utilized for the selective detection of Ni(ii) using the peptide-Fe(ii) complex. Repeated switching of the helical structure was also achieved by multiple additions of divalent metal ions to the peptide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amines / chemistry*
  • Amino Acid Sequence
  • Models, Molecular
  • Molecular Sequence Data
  • Organometallic Compounds / chemistry
  • Peptides / chemistry*
  • Picolinic Acids / chemistry*
  • Protein Structure, Secondary
  • Transition Temperature

Substances

  • 2,2'-dipicolylamine
  • Amines
  • Organometallic Compounds
  • Peptides
  • Picolinic Acids