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Using this method, the active site preferences of PP1 and PP2AB55 are investigated and compared to mitotic exit substrates identified by phosphoproteomics

We have now extended this assay to quantify proteindependent dephosphorylation by synthesizing 94 phosphorylated Ser or Thr containing peptides with basic, acidic, or hydrophobic amino acids surrounding the phosphorylation site on MRBLEs with a 1:1 linkage between the identity of the synthesized peptide and the embedded spectral code (Fig 1A)

Patients should inform their provider about all medications, supplements, and peptides they are taking

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Retrieved January 28, 2022