Preparation of a cross-linked porous protein crystal containing Ru carbonyl complexes as a CO-releasing extracellular scaffold

Inorg Chem. 2015 Jan 5;54(1):215-20. doi: 10.1021/ic502159x. Epub 2014 Dec 15.

Abstract

Protein crystals generally are stable solid protein assemblies. Certain protein crystals are suitable for use as nanovessels for immobilizing metal complexes. Here we report the preparation of ruthenium carbonyl-incorporated cross-linked hen egg white lysozyme crystals (Ru·CL-HEWL). Ru·CL-HEWL retains a Ru carbonyl moiety that can release CO, although a composite of Ru carbonyl-HEWL dissolved in buffer solution (Ru·HEWL) does not release CO. We found that treatment of cells with Ru·CL-HEWL significantly increased nuclear factor kappa B (NF-κB) activity as a cellular response to CO. These results demonstrate that Ru·CL-HEWL has potential for use as an artificial extracellular scaffold suitable for transport and release of a gas molecule.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Transport
  • Carbon Monoxide / chemistry*
  • Carbon Monoxide / pharmacology
  • Chickens
  • Coordination Complexes / chemistry*
  • Coordination Complexes / pharmacology
  • Cross-Linking Reagents / chemistry
  • Crystallization
  • Crystallography, X-Ray
  • Egg White / chemistry
  • Gene Expression / drug effects
  • Genes, Reporter
  • Glutaral / chemistry
  • HEK293 Cells
  • Humans
  • Luciferases / genetics
  • Luciferases / metabolism
  • Muramidase / chemistry*
  • Myoglobin / chemistry
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • Porosity
  • Ruthenium / chemistry*

Substances

  • Coordination Complexes
  • Cross-Linking Reagents
  • Myoglobin
  • NF-kappa B
  • Carbon Monoxide
  • Ruthenium
  • Luciferases
  • Muramidase
  • Glutaral