Literature DB >> 17608512

New candidate targets of AMP-activated protein kinase in murine brain revealed by a novel multidimensional substrate-screen for protein kinases.

Roland D Tuerk1, Ramon F Thali, Yolanda Auchli, Helene Rechsteiner, René A Brunisholz, Uwe Schlattner, Theo Wallimann, Dietbert Neumann.   

Abstract

AMP-activated protein kinase (AMPK) is a heterotrimeric serine/threonine kinase that is involved in the maintenance of energy homeostasis and recovery from metabolic stresses both at the cellular and whole body level. AMPK is found in all tissues examined so far, and a number of downstream targets have been identified. Recent work suggests that AMPK has specialized functions in the brain, such as involvement in appetite control. Nevertheless, brain-specific substrates of AMPK are unknown. Here, we performed a proteomic in vitro screen to identify new putative AMPK targets in brain. Prefractionation of murine brain lysates by liquid chromatography, utilizing four different, serially connected columns with different chemistries was found to be superior to a single column method. A pilot screen involving incubation of small volumes of individual fractions with radiolabeled ATP in the presence or absence of active AMPK, followed by one-dimensional SDS-PAGE and autoradiography, revealed the presence of potential AMPK substrates in a number of different fractions. On the basis of these results, several kinase assays were repeated with selected fractions on a preparative scale. Following separation of the radiolabeled proteins by two-dimensional electrophoresis and comparison of samples with or without added AMPK by differential autoradiography, 53 AMPK-specific phospho-spots were detected and excised. Thereof, 26 unique proteins were identified by mass spectrometry and were considered as new potential downstream targets of AMPK. Kinase assays with 14 highly purified candidate substrate proteins confirmed that at least 12 were direct targets of AMPK in vitro. Although the physiological consequences of these phosphorylation events remain to be established, hypotheses concerning the most intriguing potential targets of AMPK that have been identified by this search are discussed herein. Our data suggests that signaling by AMPK in brain is likely to be involved in the regulation of pathways that have not yet been linked to this kinase.

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Year:  2007        PMID: 17608512     DOI: 10.1021/pr070160a

Source DB:  PubMed          Journal:  J Proteome Res        ISSN: 1535-3893            Impact factor:   4.466


  13 in total

1.  AMP-activated Protein Kinase Up-regulates Mitogen-activated Protein (MAP) Kinase-interacting Serine/Threonine Kinase 1a-dependent Phosphorylation of Eukaryotic Translation Initiation Factor 4E.

Authors:  Xiaoqing Zhu; Vivian Dahlmans; Ramon Thali; Christian Preisinger; Benoit Viollet; J Willem Voncken; Dietbert Neumann
Journal:  J Biol Chem       Date:  2016-07-13       Impact factor: 5.157

2.  AMPK Preferentially Depresses Retrograde Transport of Axonal Mitochondria during Localized Nutrient Deprivation.

Authors:  Orla Watters; Niamh M C Connolly; Hans-Georg König; Heiko Düssmann; Jochen H M Prehn
Journal:  J Neurosci       Date:  2020-05-11       Impact factor: 6.167

3.  Vacuolar H+-ATPase apical accumulation in kidney intercalated cells is regulated by PKA and AMP-activated protein kinase.

Authors:  Fan Gong; Rodrigo Alzamora; Christy Smolak; Hui Li; Sajid Naveed; Dietbert Neumann; Kenneth R Hallows; Núria M Pastor-Soler
Journal:  Am J Physiol Renal Physiol       Date:  2010-02-10

Review 4.  Effects of AMP-activated protein kinase in cerebral ischemia.

Authors:  Jun Li; Louise D McCullough
Journal:  J Cereb Blood Flow Metab       Date:  2009-12-16       Impact factor: 6.200

Review 5.  AMPK: An Energy-Sensing Pathway with Multiple Inputs and Outputs.

Authors:  D Grahame Hardie; Bethany E Schaffer; Anne Brunet
Journal:  Trends Cell Biol       Date:  2015-11-23       Impact factor: 20.808

6.  AMP-activated protein kinase inhibits alkaline pH- and PKA-induced apical vacuolar H+-ATPase accumulation in epididymal clear cells.

Authors:  Kenneth R Hallows; Rodrigo Alzamora; Hui Li; Fan Gong; Christy Smolak; Dietbert Neumann; Núria M Pastor-Soler
Journal:  Am J Physiol Cell Physiol       Date:  2009-02-11       Impact factor: 4.249

7.  AMP-activated protein kinase regulates the vacuolar H+-ATPase via direct phosphorylation of the A subunit (ATP6V1A) in the kidney.

Authors:  Rodrigo Alzamora; Mohammad M Al-Bataineh; Wen Liu; Fan Gong; Hui Li; Ramon F Thali; Yolanda Joho-Auchli; René A Brunisholz; Lisa M Satlin; Dietbert Neumann; Kenneth R Hallows; Núria M Pastor-Soler
Journal:  Am J Physiol Renal Physiol       Date:  2013-07-17

8.  Mild Glucose Starvation Induces KDM2A-Mediated H3K36me2 Demethylation through AMPK To Reduce rRNA Transcription and Cell Proliferation.

Authors:  Yuji Tanaka; Hirohisa Yano; Sachiko Ogasawara; Sho-Ichi Yoshioka; Hiromi Imamura; Kengo Okamoto; Makoto Tsuneoka
Journal:  Mol Cell Biol       Date:  2015-09-28       Impact factor: 4.272

9.  AMPK Protein Interaction Analyses by Yeast Two-Hybrid.

Authors:  Pascual Sanz; Rosa Viana; Maria Adelaida Garcia-Gimeno
Journal:  Methods Mol Biol       Date:  2018

10.  PKA regulates vacuolar H+-ATPase localization and activity via direct phosphorylation of the a subunit in kidney cells.

Authors:  Rodrigo Alzamora; Ramon F Thali; Fan Gong; Christy Smolak; Hui Li; Catherine J Baty; Carol A Bertrand; Yolanda Auchli; René A Brunisholz; Dietbert Neumann; Kenneth R Hallows; Núria M Pastor-Soler
Journal:  J Biol Chem       Date:  2010-06-04       Impact factor: 5.157

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