Polycystin-1: immunoaffinity isolation and characterisation by mass spectrometry

FEBS Lett. 2001 Sep 14;505(2):313-6. doi: 10.1016/s0014-5793(01)02842-3.

Abstract

Polycystin-1 is a putative 460 kDa membrane protein with a unique structure and is possibly representative of a new family of proteins. Its structure suggests an involvement in cell signalling and cell-matrix interactions. The amino acid sequence of polycystin-1 has to date been predicted from its gene sequence. This, to our knowledge, is the first report of the isolation and analysis of polycystin-1 at the protein level using mass spectrometry to confirm its predicted structure. The availability of purified polycystin-1 will allow a new approach to unravelling the complexity of the cell-cell and cell-matrix interactions of this large molecule in normal cells and its perturbation in disease.

MeSH terms

  • Blotting, Western
  • Cell Line
  • Electrophoresis, Polyacrylamide Gel
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • Hydrogen-Ion Concentration
  • Mass Spectrometry / methods*
  • Protein Binding
  • Protein Conformation
  • Proteins / chemistry*
  • Proteins / isolation & purification*
  • Signal Transduction
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • TRPP Cation Channels
  • Trypsin / metabolism

Substances

  • Proteins
  • TRPP Cation Channels
  • polycystic kidney disease 1 protein
  • Trypsin