Proteome analysis of microtubule-associated proteins and their interacting partners from mammalian brain

Amino Acids. 2011 Jul;41(2):363-85. doi: 10.1007/s00726-010-0649-5. Epub 2010 Jun 22.

Abstract

The microtubule (MT) cytoskeleton is essential for a variety of cellular processes. MTs are finely regulated by distinct classes of MT-associated proteins (MAPs), which themselves bind to and are regulated by a large number of additional proteins. We have carried out proteome analyses of tubulin-rich and tubulin-depleted MAPs and their interacting partners isolated from bovine brain. In total, 573 proteins were identified giving us unprecedented access to brain-specific MT-associated proteins from mammalian brain. Most of the standard MAPs were identified and at least 500 proteins have been reported as being associated with MTs. We identified protein complexes with a large number of subunits such as brain-specific motor/adaptor/cargo complexes for kinesins, dynein, and dynactin, and proteins of an RNA-transporting granule. About 25% of the identified proteins were also found in the synaptic vesicle proteome. Analysis of the MS/MS data revealed many posttranslational modifications, amino acid changes, and alternative splice variants, particularly in tau, a key protein implicated in Alzheimer's disease. Bioinformatic analysis of known protein-protein interactions of the identified proteins indicated that the number of MAPs and their associated proteins is larger than previously anticipated and that our database will be a useful resource to identify novel binding partners.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Brain / metabolism*
  • Cattle
  • Humans
  • Microtubules / metabolism*
  • Molecular Sequence Data
  • Molecular Weight
  • Phosphoproteins / chemistry
  • Phosphoproteins / isolation & purification
  • Phosphoproteins / metabolism
  • Protein Interaction Mapping*
  • Protein Isoforms / metabolism
  • Protein Processing, Post-Translational
  • Proteome / metabolism*
  • Tandem Mass Spectrometry
  • Tubulin / metabolism*

Substances

  • Phosphoproteins
  • Protein Isoforms
  • Proteome
  • Tubulin