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1MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences,University of Dundee, 2The Michael J. Fox Foundation for Parkinson’s Research, 3Department of Medical and Molecular Genetics,Indiana University School of Medicine, 4Morton and Gloria Shulman Movement Disorders Centre and the Edmond J. Safra Program in Parkinson’s Disease, Toronto Western Hospital,University of Toronto, 5Division of Cell Signalling and Immunology, School of Life Sciences,University of Dundee, 6Division of Molecular and Clinical Medicine, School of Medicine, Ninewells Hospital and Medical School,University of Dundee
Chapters
- 00:01Introduction
- 00:48Neutrophil Isolation from Human Peripheral Blood
- 07:18LRRK2 Kinase Inhibitor Treatment
- 10:33Results
- 12:14Conclusion
Mutationen im Leucin-reichen Repeatkinase-2-Gen (LRRK2) verursachen eine erbliche Parkinson-Krankheit. Wir haben eine einfache und robuste Methode zur Beurteilung der LRRK2-kontrollierten Phosphorylierung von Rab10 bei menschlichen peripheren Blutneutrophilen entwickelt. Dies kann helfen, Personen mit erhöhter LRRK2-Kinase-Signalweg-Aktivität zu identifizieren.
