A Surface Biotinylation Strategy for Reproducible Plasma Membrane Protein Purification and Tracking of Genetic and Drug-Induced Alterations - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Journal of Proteome Research Année : 2016

A Surface Biotinylation Strategy for Reproducible Plasma Membrane Protein Purification and Tracking of Genetic and Drug-Induced Alterations

Katrin Hörmann
  • Fonction : Auteur
Alexey Stukalov
  • Fonction : Auteur
André Müller
  • Fonction : Auteur
Leonhard Heinz
  • Fonction : Auteur
Giulio Superti-Furga
  • Fonction : Auteur
  • PersonId : 915263
Keiryn Bennett
  • Fonction : Auteur

Résumé

Plasma membrane (PM) proteins contribute to the identity of a cell, mediate contact and communication, and account for more than two-thirds of known drug targets.1-8 In the past years, several protocols for the proteomic profiling of PM proteins have been described. Nevertheless, comparative analyses have mainly focused on different variations of one approach.9-11 We compared sulfo-NHS-SS-biotinylation, aminooxy-biotinylation, and surface coating with silica beads to isolate PM proteins for subsequent analysis by one-dimensional gel-free liquid chromatography mass spectrometry. Absolute and relative numbers of PM proteins and reproducibility parameters on a qualitative and quantitative level were assessed. Sulfo-NHS-SS-biotinylation outperformed aminooxy-biotinylation and surface coating using silica beads for most of the monitored criteria. We further simplified this procedure by a competitive biotin elution strategy achieving an average PM annotated protein fraction of 54% (347 proteins). Computational analysis using additional databases and prediction tools revealed that in total over 90% of the purified proteins were associated with the PM, mostly as interactors. The modified sulfo-NHS-SS-biotinylation protocol was validated by tracking changes in the plasma membrane proteome composition induced by genetic alteration and drug treatment. Glycosylphosphatidylinositol (GPI)-anchored proteins were depleted in PM purifications from cells deficient in the GPI transamidase component PIGS, and treatment of cells with tunicamycin significantly reduced the abundance of N-glycoproteins in surface purifications.
Fichier non déposé

Dates et versions

hal-02296681 , version 1 (25-09-2019)

Identifiants

Citer

Katrin Hörmann, Alexey Stukalov, André Müller, Leonhard Heinz, Giulio Superti-Furga, et al.. A Surface Biotinylation Strategy for Reproducible Plasma Membrane Protein Purification and Tracking of Genetic and Drug-Induced Alterations. Journal of Proteome Research, 2016, 15 (2), pp.647-658. ⟨10.1021/acs.jproteome.5b01066⟩. ⟨hal-02296681⟩
105 Consultations
0 Téléchargements

Altmetric

Partager

Gmail Facebook X LinkedIn More