Your browser doesn't support javascript.
loading
A bead-based western for high-throughput cellular signal transduction analyses.
Treindl, Fridolin; Ruprecht, Benjamin; Beiter, Yvonne; Schultz, Silke; Döttinger, Anette; Staebler, Annette; Joos, Thomas O; Kling, Simon; Poetz, Oliver; Fehm, Tanja; Neubauer, Hans; Kuster, Bernhard; Templin, Markus F.
Afiliação
  • Treindl F; NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.
  • Ruprecht B; Pharmaceutical Biotechnology, Eberhard-Karls-Universität Tübingen, Tübingen, 72770 Reutlingen, Germany.
  • Beiter Y; Chair for Proteomics and Bioanalytics, Center of Life and Food Sciences Weihenstephan, Technische Universität München, 85354 Freising, Germany.
  • Schultz S; Center for Integrated Protein Science Munich, 85354 Freising, Germany.
  • Döttinger A; NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.
  • Staebler A; Pharmaceutical Biotechnology, Eberhard-Karls-Universität Tübingen, Tübingen, 72770 Reutlingen, Germany.
  • Joos TO; Department of Obstetrics and Gynecology, Medical Faculty and University Hospital of the Heinrich-Heine University Duesseldorf, 40225 Düsseldorf, Germany.
  • Kling S; NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.
  • Poetz O; Department of Pathology, University Hospital Tübingen, 72076 Tübingen, Germany.
  • Fehm T; NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.
  • Neubauer H; NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.
  • Kuster B; NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.
  • Templin MF; Department of Obstetrics and Gynecology, Medical Faculty and University Hospital of the Heinrich-Heine University Duesseldorf, 40225 Düsseldorf, Germany.
Nat Commun ; 7: 12852, 2016 Sep 23.
Article em En | MEDLINE | ID: mdl-27659302
Dissecting cellular signalling requires the analysis of large number of proteins. The DigiWest approach we describe here transfers the western blot to a bead-based microarray platform. By combining gel-based protein separation with immobilization on microspheres, hundreds of replicas of the initial blot are created, thus enabling the comprehensive analysis of limited material, such as cells collected by laser capture microdissection, and extending traditional western blotting to reach proteomic scales. The combination of molecular weight resolution, sensitivity and signal linearity on an automated platform enables the rapid quantification of hundreds of specific proteins and protein modifications in complex samples. This high-throughput western blot approach allowed us to identify and characterize alterations in cellular signal transduction that occur during the development of resistance to the kinase inhibitor Lapatinib, revealing major changes in the activation state of Ephrin-mediated signalling and a central role for p53-controlled processes.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article