A constitutive form of heat-shock protein 70 is located in the outer membranes of mitochondria from rat liver

FEBS Lett. 1993 Oct 18;332(3):277-81. doi: 10.1016/0014-5793(93)80649-f.

Abstract

HSP73, the constitutive form of heat-shock protein 70, has been implicated in the translocation of preproteins across the mitochondrial membranes, being required for maintaining mitochondrial preproteins in an import competent conformation. Here we report that highly purified mitochondrial outer membranes contain a protein indistinguishable from HSP73 as a tightly associated peripheral component of the membrane. This membrane form of HSP73 was photolabelled with [alpha-32P]ATP and could be released from the outer membrane with sodium carbonate, but not after incubation of the membranes with salt or with ATP. A sensitive immunoassay with an anti-HSP73 monoclonal antibody, revealed the association of HSP73 with mitochondrial outer membrane vesicles at a level similar to that of preprotein import receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Electrophoresis, Gel, Two-Dimensional
  • Electrophoresis, Polyacrylamide Gel
  • Enzyme-Linked Immunosorbent Assay
  • Heat-Shock Proteins / analysis*
  • Heat-Shock Proteins / isolation & purification
  • Heat-Shock Proteins / metabolism
  • Immunoblotting
  • Intracellular Membranes / chemistry*
  • Intracellular Membranes / metabolism
  • Membrane Proteins / chemistry
  • Membrane Proteins / metabolism
  • Mitochondria, Liver / chemistry*
  • Mitochondria, Liver / metabolism
  • Molecular Weight
  • Rats
  • Submitochondrial Particles / chemistry*
  • Submitochondrial Particles / metabolism

Substances

  • Heat-Shock Proteins
  • Membrane Proteins
  • Adenosine Triphosphate