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Tumor necrosis factor (TNF)-functionalized nanostructured particles for the stimulation of membrane TNF-specific cell responses

  • Susanne Bryde
  • , Ingo Grunwald
  • , Angela Hammer
  • , Anja Krippner-Heidenreich
  • , Thomas Schiestel
  • , Herwig Brunner
  • , Günter E.M. Tovar
  • , Klaus Pfizenmaier
  • , Peter Scheurich

Research output: Contribution to journalArticlepeer-review

31 Citations (Scopus)

Abstract

Most members of the tumor necrosis factor (TNF) ligand family occur in both a membrane-bound and a soluble form, which can possess differential bioactivities. The aim of this work was the construction of a synthetic-biological hybrid system consisting of chemically nanostructured core-shell particles with a diameter of 100 nm, 1 μm, or 10 μm and the cytokine TNF to obtain a tool that mimics the bioactivity of naturally occurring membrane-bound TNF. Synthetic core-shell nanoparticles consisting of an inorganic silica core and an ultrathin organic shell bearing a maleimide group at the shell surface which allowed for a covalent and site-directed coupling of CysHisTNF mutants were prepared. The TNF mutants were modified at the N-terminus by PCR cloning by introducing a His-Tag for purification and a free cysteine group for reaction with the particle-attached maleimide group. The resulting nanostructured hybrid particles initiated strong TNF receptor type 2 specific responses, otherwise only seen for the membrane-bound form of TNF, but not the soluble cytokine, thus clearly demonstrating new and membrane TNF-like properties of the bioconjugated soluble TNF.

Original languageEnglish
Pages (from-to)1459-1467
Number of pages9
JournalBioconjugate Chemistry
Volume16
Issue number6
DOIs
Publication statusPublished - 2005
Externally publishedYes

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