Polyvalent display of monosaccharides on ferritin protein cage nanoparticles for the recognition and binding of cell-surface lectins

Macromol Biosci. 2014 May;14(5):619-25. doi: 10.1002/mabi.201300528. Epub 2014 Feb 10.

Abstract

Carbohydrate-lectin interactions are important in many biological events. Endogenous cell-surface lectins are attractive markers for the recognition and targeting. Human ferritin protein cage nanoparticles (HFPCNs) are prepared as delivery nanoplatforms and two different types of monosaccharide derivatives; maleimido group terminated-mannopyranoside and galactopyranoside. Uniform and polyvalent displays of mannoses or galactoses on the surface of HFPCNs are achieved by using site-specific thiol-maleimide Michael-type addition. Mannose- or galactose-displaying HFPCNs recognize and tightly bind to DC-SIGN or ASGP-R lectins on the surface of the mammalian cells, DCEK or HepG2 cells.

Keywords: cell-surface lectins; delivery nanoplatforms; glycoconjugates; polyvalent display; protein cages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Chromatography, Gel
  • Drug Delivery Systems / methods*
  • Ferritins / chemistry*
  • Glycosides / chemical synthesis
  • Humans
  • Lectins / metabolism*
  • Mass Spectrometry
  • Membrane Proteins / metabolism*
  • Metal Nanoparticles / chemistry*
  • Mice
  • Microscopy, Fluorescence
  • Models, Molecular*
  • Molecular Structure
  • Monosaccharides / chemistry
  • Monosaccharides / metabolism*
  • Mutagenesis
  • Surface Plasmon Resonance

Substances

  • Glycosides
  • Lectins
  • Membrane Proteins
  • Monosaccharides
  • Ferritins