Precise engineering of apoferritin through site-specific host-guest binding

Chem Commun (Camb). 2020 Nov 4;56(85):12897-12900. doi: 10.1039/d0cc05382a. Epub 2020 Sep 30.

Abstract

The surface engineering of the apoferritin shell by means of traditional chemical modifications usually suffers from site inaccuracy and insufficient conjugation. This report describes a non-covalent method for precise modulation of the apoferritin surface without alteration of amino acid residues. A bifunctional macromolecule, structured as azide-poly(ethylene glycol)-porphyrin (termed TPA), was synthesized. TPA was observed to be able to recognize and bind apoferritin in a 12 : 1 stoichiometry with a higher binding affinity than arachidonate, thanks to the specific host-guest interaction between the pocket of each two-fold channel and the porphyrin moiety. This method allows for site-specific engineering of the apoferritin surface with on demand functionalities and optimization of drug encapsulation.

MeSH terms

  • Apoferritins / chemistry*
  • Azides / chemistry*
  • Binding Sites
  • Models, Molecular
  • Molecular Structure
  • Polyethylene Glycols / chemistry*
  • Porphyrins / chemistry*
  • Protein Engineering*

Substances

  • Azides
  • Porphyrins
  • Polyethylene Glycols
  • Apoferritins