Characterization of the in vitro phosphorylation of human tau by tau protein kinase II (cdk5/p20) using mass spectrometry

J Neurochem. 2001 Feb;76(4):1221-32. doi: 10.1046/j.1471-4159.2001.00130.x.


Hyperphosphorylated tau is an integral part of the neurofibrillary tangles that form within neuronal cell bodies, and tau protein kinase II is reported to play a role in the pathogenesis of Alzheimer's disease. Recently, we reported that tau protein kinase II (cdk5/p20)-phosphorylated human tau inhibits microtubule assembly, and tau protein kinase II (cdk5/p20) phosphorylation of microtubule-associated tau results in dissociation of phosphorylated tau from the microtubules and tubulin depolymerization. In the studies reported here, a combination of mass spectrometric techniques was used to study the phosphorylation of human recombinant tau by recombinant tau protein kinase II (cdk5/p20) in vitro. The extent of phosphorylation was determined by measuring the molecular mass of phosphorylated tau using mass spectrometry. Reaction of human recombinant tau with tau protein kinase II (cdk5/p20) resulted in the formation of two major species containing either five or six phosphate groups. The specific amino acid residues phosphorylated were determined by analyzing tryptic peptides by tandem mass spectrometry via either MALDI/TOF post-source decay or by electrospray tandem mass spectrometry. Based on these experiments, we conclude that tau protein kinase II (cdk5/p20) can phosphorylate human tau at Thr(181), Thr(205), Thr(212), Thr(217), Ser(396) and Ser(404).

MeSH terms

  • Amino Acid Sequence
  • Binding Sites / physiology
  • Cyclin-Dependent Kinase 5
  • Humans
  • Molecular Weight
  • Phosphorylation
  • Protein Serine-Threonine Kinases / metabolism*
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism
  • Sequence Analysis, Protein
  • Spectrometry, Mass, Electrospray Ionization*
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization*
  • tau Proteins / chemistry
  • tau Proteins / metabolism*


  • Recombinant Proteins
  • tau Proteins
  • Cyclin-Dependent Kinase 5
  • Protein Serine-Threonine Kinases
  • tau protein kinase II