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- W2054954966 abstract "The heterotrimeric enzyme AMP-activated protein kinase (AMPK) is a major metabolic factor that regulates the homeostasis of cellular energy. In particular, AMPK mediates the insulin resistance that is associated with type 2 diabetes. Generally, cellular processes require tight regulation of protein kinases, which is effected through their formation of complex with other proteins and substrates. Despite their critical function in regulation and pathogenesis, there are limited data on the interaction of protein kinases. To identify proteins that interact with AMPK, we performed large-scale affinity purification (AP)-mass spectrometry (MS) of the AMPK-α1 and -β1 subunits. Through a comprehensive analysis, using a combination of immunoprecipitaion and ion trap mass spectrometry, we identified 381 unique proteins in the AMPKα/β interactomes: 325 partners of AMPK-α1 and 243 for AMPK-β1. Further, we identified 196 novel protein-protein interactions with AMPK-α1 and AMPK-β1. Notably, in our bioinformatics analysis, the novel interaction partners mediated functions that are related to the regulation of actin organization. Specifically, several such proteins were linked to pancreatic beta-cell functions, including glucose-stimulated insulin secretion, beta-cell development, beta-cell differentiation, and cell-cell communication." @default.
- W2054954966 created "2016-06-24" @default.
- W2054954966 creator A5022694995 @default.
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- W2054954966 creator A5089590792 @default.
- W2054954966 date "2014-03-14" @default.
- W2054954966 modified "2023-10-13" @default.
- W2054954966 title "Interactome analysis of AMP-activated protein kinase (AMPK)-α1 and -β1 in INS-1 pancreatic beta-cells by affinity purification-mass spectrometry" @default.
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- W2054954966 doi "https://doi.org/10.1038/srep04376" @default.
- W2054954966 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3953747" @default.
- W2054954966 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24625528" @default.
- W2054954966 hasPublicationYear "2014" @default.
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