Proteomics of bovine mitochondrial RNA-binding proteins: HES1/KNP-I is a new mitochondrial resident protein

J Proteome Res. 2005 Jan-Feb;4(1):43-52. doi: 10.1021/pr049872g.

Abstract

Proteomic analysis of bovine mitochondrial proteins with affinity to polyAdenylate or polyUridylate was performed in an effort to identify novel RNA-binding mitochondrial proteins. We have used 2D gel electrophoresis and MALDI-QqTOF mass spectrometry to identify a total of 64 proteins, of which 51 have defined mitochondrial function including 6 known RNA-binding proteins. HES1/KNP-I from the polyA-binding fraction of mitochondrial Triton extract showed exclusive mitochondrial localization when expressed in GFP-tagged form. The HES1/KNP-I gene is on human chromosome 21q22.3 and may be involved in several disorders mapped to that region. Thus, HES1/KNP-I is a proven mitochondrial resident protein with apparent tight membrane association and tentative RNA-binding properties.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Chromatography, Affinity
  • Electrophoresis, Gel, Two-Dimensional
  • Mitochondrial Proteins / analysis
  • Mitochondrial Proteins / isolation & purification*
  • Octoxynol
  • Poly A
  • Poly U
  • Proteomics / methods*
  • RNA-Binding Proteins / analysis
  • RNA-Binding Proteins / isolation & purification*
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

Substances

  • Mitochondrial Proteins
  • RNA-Binding Proteins
  • Poly A
  • Poly U
  • Octoxynol