Literature DB >> 21638028

Novel screening cascade identifies MKK4 as key kinase regulating Tau phosphorylation at Ser422.

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.

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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


  38 in total

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6.  Pseudophosphorylation of tau protein alters its ability for self-aggregation.

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8.  Phosphorylation of Tau at S422 is enhanced by Abeta in TauPS2APP triple transgenic mice.

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2.  Phosphorylation in two discrete tau domains regulates a stepwise process leading to postsynaptic dysfunction.

Authors:  Peter J Teravskis; Breeta R Oxnard; Eric C Miller; Lisa Kemper; Karen H Ashe; Dezhi Liao
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3.  The earliest tau dysfunction in Alzheimer's disease? Tau phosphorylated at s422 as a toxic seed.

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5.  Acute inhibition of the CNS-specific kinase TTBK1 significantly lowers tau phosphorylation at several disease relevant sites.

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6.  Plasma protein biomarkers of Alzheimer's disease endophenotypes in asymptomatic older twins: early cognitive decline and regional brain volumes.

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Review 7.  Use of okadaic acid to identify relevant phosphoepitopes in pathology: a focus on neurodegeneration.

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