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

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

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

    roland d tuerkRoland D Tuerk,ramon f thaliRamon F Thali,yolanda auchliYolanda Auchli,helene rechsteinerHelene Rechsteiner, brunisholz Brunisholz,uwe schlattnerUwe Schlattner,theo wallimannTheo Wallimann,dietbert neumannDietbert Neumann,

    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.

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

    rd tuerkRD Tuerk,rf thaliRF Thali,y auchliY Auchli,h rechsteinerH Rechsteiner,ra brunisholzRA Brunisholz,u schlattnerU Schlattner,t wallimannT Wallimann,d neumannD Neumann,

    For similar abstracts research abstracts see: abstracts research

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

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of proteome research

    VOLUME: 6

    Page Numbers: 3266-77

    Journal Abbreviation: J. Proteome Res.

    ISSN: 1535-3893

    DAY: 4

    MONTH: 07

    YEAR: 2007

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

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    LANGUAGE: eng

    NlmUniqueID: 101128775

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

    AFFILIATION: Institutes of Cell Biology and Molecular Biology & Biophysics, ETH Zurich, 8093 Zurich, Switzerland.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Proteome Res

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