PKA phosphorylates catalytic α‐ and regulatory β‐subunits of AMPK at multiple sites. PKA phosphorylates catalytic α‐ and regulatory β‐subunits of AMPK.

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PKA phosphorylates catalytic α‐ and regulatory β‐subunits of AMPK at multiple sites. PKA phosphorylates catalytic α‐ and regulatory β‐subunits of AMPK at multiple sites. (A) PKA phosphorylates AMPK in vitro. Autoradiograph of α1β1γ1 catalytically inactive AMPK(D157A) complexes incubated in the presence of [γ‐32P]ATP with either the cAMP‐dependent PKA holoenzyme, PKA[holo], or the constitutively active, cAMP independent, catalytic domain of PKA, PKA[cat]. Arrows indicate phosphorylated AMPK(D157) at the α1‐ and β1‐subunits. (B) Mass fingerprinting of isolated phosphopeptides derived from HPLC was performed by MALDI‐ToF MS. Peptides differing by +80 Da (HPO3) from computed masses were then selected for MS/MS and phosphorylation was confirmed by a neutral loss of −98 Da (H3PO4) during fragmentation. Further verification of the phosphosites was attempted by solid‐phase sequencing of the radiolabelled peptides. After each cycle of N‐terminal Edman degradation, liberated single amino acids were collected and spotted onto DEAE cellulose. The respective phosphorylated residues were then detected by autoradiography. The annotated mass spectra indicates the phosphorylated residues of AMPKα1 pSer‐173, pSer‐485 and pSer‐497. (C) As in (B) but related to AMPKβ1 pSer‐24. Dha, dehydroala. (D) Analysis of AMPKα1 phosphorylation site mutants. Purified AMPK(D157A) (control), or the indicated serine to alanine mutants thereof, were incubated with PKA in the presence of [γ‐32P]ATP and processed for SDS–PAGE and autoradiography. (E) Verification of in vitro AMPK β1‐phosphorylation sites by mutational analysis. Catalytically inactive AMPK(D157A) complexes containing a regulatory β1‐subunit mutated at Ser‐24 and/or Ser‐25 were incubated with [γ‐32P]ATP in the presence or absence of PKA. Phosphorylation was visualized by SDS–PAGE and autoradiography. PKA was unable to phosphorylate AMPKβ1 mutated in Ser‐24 (lane 4) but not Ser‐25 (lane 6), showing that only Ser‐24 is targeted by PKA. Control, AMPK(D157A) containing no additional mutations. Immunoblots are representative of at least three independent experiments. Nabil Djouder et al. EMBO J. 2010;29:469-481 © as stated in the article, figure or figure legend