Unknown

Dataset Information

0

Global Phosphoproteomic Analysis of Human Skeletal Muscle Reveals a Network of Exercise-Regulated Kinases and AMPK Substrates.


ABSTRACT: Exercise is essential in regulating energy metabolism and whole-body insulin sensitivity. To explore the exercise signaling network, we undertook a global analysis of protein phosphorylation in human skeletal muscle biopsies from untrained healthy males before and after a single high-intensity exercise bout, revealing 1,004 unique exercise-regulated phosphosites on 562 proteins. These included substrates of known exercise-regulated kinases (AMPK, PKA, CaMK, MAPK, mTOR), yet the majority of kinases and substrate phosphosites have not previously been implicated in exercise signaling. Given the importance of AMPK in exercise-regulated metabolism, we performed a targeted in vitro AMPK screen and employed machine learning to predict exercise-regulated AMPK substrates. We validated eight predicted AMPK substrates, including AKAP1, using targeted phosphoproteomics. Functional characterization revealed an undescribed role for AMPK-dependent phosphorylation of AKAP1 in mitochondrial respiration. These data expose the unexplored complexity of acute exercise signaling and provide insights into the role of AMPK in mitochondrial biochemistry.

SUBMITTER: Hoffman NJ 

PROVIDER: S-EPMC4635038 | biostudies-literature | 2015 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications


Exercise is essential in regulating energy metabolism and whole-body insulin sensitivity. To explore the exercise signaling network, we undertook a global analysis of protein phosphorylation in human skeletal muscle biopsies from untrained healthy males before and after a single high-intensity exercise bout, revealing 1,004 unique exercise-regulated phosphosites on 562 proteins. These included substrates of known exercise-regulated kinases (AMPK, PKA, CaMK, MAPK, mTOR), yet the majority of kinas  ...[more]

Similar Datasets

| S-EPMC5369209 | biostudies-literature
2016-06-29 | PXD001543 | Pride
2017-03-29 | MSV000080777 | MassIVE
| S-EPMC6449061 | biostudies-literature
| S-EPMC3616265 | biostudies-literature
| S-EPMC2815736 | biostudies-literature
| S-EPMC4563030 | biostudies-literature
| S-EPMC6098843 | biostudies-literature
2022-07-18 | PXD031049 | Pride
2022-10-25 | PXD031372 | Pride