Development of protein-cage-based delivery nanoplatforms by polyvalently displaying β-cyclodextrins on the surface of ferritins through copper(I)-catalyzed azide/alkyne cycloaddition

Macromol Biosci. 2012 Nov;12(11):1452-8. doi: 10.1002/mabi.201200178. Epub 2012 Sep 10.

Abstract

Protein cages are spherical hollow macromolecules that are attractive platforms for the construction of nanoscale cargo delivery vehicles. Human heavy-chain ferritin (HHFn) is modified genetically to control the number and position of functional groups per cage. 24 β-CDs are conjugated precisely to the modified HHFn in specific locations through thiol-maleimide Michael-type addition followed by copper(I)-catalyzed azide/alkyne cycloaddition (CuAAC). The resulting human ferritins displaying β-CDs (β-CD-C90 HHFn) can form inclusion complexes with FITC-AD, which can slowly release the guest molecule reversibly in a buffer solution via non-covalent β-CD/AD interactions. β-CD-C90 HHFn can potentially be used as delivery vehicles for insoluble drugs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry*
  • Apoferritins / chemistry*
  • Azides / chemistry*
  • Catalysis
  • Copper / chemistry*
  • Cross-Linking Reagents
  • Cycloaddition Reaction
  • Drug Carriers / chemical synthesis*
  • Humans
  • beta-Cyclodextrins / chemistry*

Substances

  • Alkynes
  • Azides
  • Cross-Linking Reagents
  • Drug Carriers
  • beta-Cyclodextrins
  • Copper
  • Apoferritins