Characterization of the interactions between inhibitor-1 and recombinant PP1 by NMR spectroscopy

Sci Rep. 2018 Jan 8;8(1):50. doi: 10.1038/s41598-017-18383-x.

Abstract

Inhibitor-1 is converted into a potent inhibitor of native protein phosphatase-1 (PP1) when Thr35 is phosphorylated by cAMP-dependent protein kinase (PKA). However, PKA-phosphorylated form of inhibitor-1 displayed a weak activity in inhibition of recombinant PP1. The mechanism for the impaired activity of PKA-phosphorylated inhibitor-1 toward inhibition of recombinant PP1 remained elusive. By using NMR spectroscopy in combination with site-directed mutagenesis and inhibitory assay, we found that the interaction between recombinant PP1 and the consensus PP1-binding motif of PKA-thiophosphorylated form of inhibitor-1 was unexpectedly weak. Unlike binding to native PP1, the subdomains 1 (residues around and including the phosphorylated Thr35) and 2 (the consensus PP1-binding motif) of PKA-thiophosphorylated form of inhibitor-1 do not exhibit a synergistic effect in inhibition of recombinant PP1. This finding implied that a slight structural discrepancy exists between native and recombinant PP1, resulting in PKA-thiophosphorylated form of inhibitor-1 displaying a different affinity to native and recombinant enzyme.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclic AMP-Dependent Protein Kinases / chemistry
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Magnetic Resonance Spectroscopy*
  • Models, Molecular
  • Phosphorylation
  • Protein Binding
  • Protein Conformation
  • Protein Phosphatase 1 / chemistry*
  • Protein Phosphatase 1 / metabolism
  • Proteins / chemistry*
  • Proteins / metabolism
  • Structure-Activity Relationship

Substances

  • Proteins
  • phosphoprotein phosphatase inhibitor 1
  • Cyclic AMP-Dependent Protein Kinases
  • Protein Phosphatase 1