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Protoporphyrin IX binding and transport by recombinant mouse PBR.

Abstract
The mitochondrial 18kDa peripheral-type benzodiazepine receptor (PBR), a high affinity cholesterol binding protein, has been shown to interact with protoporphyrin IX (PPIX) and this interaction was assumed to be involved in the regulation of heme biosynthesis and porphyrin-based photodynamic therapy in cancer. In order to test this hypothesis recombinant mouse PBR was expressed in Escherichia coli. The recombinant gene product showed in E. coli protoplasts specific affinity for PPIX binding. PPIX could displace PK 11195 binding. Moreover, induced PBR protein expression in E. coli protoplasts caused an uptake of PPIX that could be completely inhibited by cholesterol and to a lesser extent inhibited by PK 11195 and Ro5-4864. These results suggest that PBR, in addition to its role in cholesterol and coproporphyrinogen III transport, is also directing the mitochondrial PPIX import, a function that can be ascribed to the 18kDa PBR protein alone.
AuthorsGregor Wendler, Peter Lindemann, Jean-Jacques Lacapère, Vassilios Papadopoulos
JournalBiochemical and biophysical research communications (Biochem Biophys Res Commun) Vol. 311 Issue 4 Pg. 847-52 (Nov 28 2003) ISSN: 0006-291X [Print] United States
PMID14623258 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Bzrp protein, mouse
  • Carrier Proteins
  • Escherichia coli Proteins
  • Integration Host Factors
  • Isoquinolines
  • Protoporphyrins
  • Receptors, GABA
  • Recombinant Proteins
  • integration host factor, E coli
  • Cholesterol
  • protoporphyrin IX
  • PK 11195
Topics
  • Animals
  • Binding, Competitive
  • Carrier Proteins
  • Cholesterol (metabolism)
  • Escherichia coli Proteins (genetics, metabolism)
  • Integration Host Factors (genetics, metabolism)
  • Isoquinolines (metabolism)
  • Mice
  • Protein Binding
  • Protein Transport (genetics, physiology)
  • Protoporphyrins (genetics, metabolism)
  • Receptors, GABA
  • Recombinant Proteins (genetics, metabolism)

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