Resolving and identifying protein components of plant mitochondrial respiratory complexes using three dimensions of gel electrophoresis

J Proteome Res. 2008 Feb;7(2):786-94. doi: 10.1021/pr700595p. Epub 2008 Jan 12.

Abstract

Analyzing highly hydrophobic proteins is a challenge for identification protocols based on gel separation and mass spectrometry. We combined Blue Native and 2D tricine gel electrophoresis to allow separation and identification of respiratory complex subunits from Arabidopsis mitochondria. We identified many of the highly hydrophobic mitochondrion-encoded subunits (GRAVY scores between +0.6 to +1.4) and also found a number of nucleus-encoded proteins associated with complex I for the first time in plants.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Arabidopsis / metabolism*
  • Arabidopsis Proteins / chemistry
  • Arabidopsis Proteins / isolation & purification
  • Arabidopsis Proteins / metabolism*
  • Cattle
  • Cell Respiration / physiology
  • Electron Transport Complex I / chemistry
  • Electron Transport Complex I / isolation & purification
  • Electron Transport Complex III / chemistry
  • Electron Transport Complex III / isolation & purification
  • Electrophoresis, Gel, Two-Dimensional
  • Humans
  • Mitochondria / chemistry
  • Mitochondria / metabolism*
  • Mitochondrial Proteins / chemistry
  • Mitochondrial Proteins / isolation & purification
  • Mitochondrial Proteins / metabolism*
  • Molecular Sequence Data
  • Spectrometry, Mass, Electrospray Ionization

Substances

  • Arabidopsis Proteins
  • Mitochondrial Proteins
  • Electron Transport Complex I
  • Electron Transport Complex III