| Literature DB >> 21638028 |
Fiona Grueninger1, Bernd Bohrmann, Klaus Christensen, Martin Graf, Doris Roth, Christian Czech.
Abstract
Phosphorylation of Tau at serine 422 promotes Tau aggregation. The kinase that is responsible for this key phosphorylation event has so far not been identified but could be a potential drug target for Alzheimer's disease. We describe here an assay strategy to identify this kinase. Using a combination of screening a library of 65'000 kinase inhibitors and in vitro inhibitor target profiling of the screening hits using the Ambit kinase platform, MKK4 was identified as playing a key role in Tau-S422 phosphorylation in human neuroblastoma cells.Entities:
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Year: 2011 PMID: 21638028 DOI: 10.1007/s11010-011-0890-6
Source DB: PubMed Journal: Mol Cell Biochem ISSN: 0300-8177 Impact factor: 3.396