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A substrate-driven allosteric switch that enhances PDI catalytic activity.

Nature communications | 2016

Protein disulfide isomerase (PDI) is an oxidoreductase essential for folding proteins in the endoplasmic reticulum. The domain structure of PDI is a-b-b'-x-a', wherein the thioredoxin-like a and a' domains mediate disulfide bond shuffling and b and b' domains are substrate binding. The b' and a' domains are connected via the x-linker, a 19-amino-acid flexible peptide. Here we identify a class of compounds, termed bepristats, that target the substrate-binding pocket of b'. Bepristats reversibly block substrate binding and inhibit platelet aggregation and thrombus formation in vivo. Ligation of the substrate-binding pocket by bepristats paradoxically enhances catalytic activity of a and a' by displacing the x-linker, which acts as an allosteric switch to augment reductase activity in the catalytic domains. This substrate-driven allosteric switch is also activated by peptides and proteins and is present in other thiol isomerases. Our results demonstrate a mechanism whereby binding of a substrate to thiol isomerases enhances catalytic activity of remote domains.

Pubmed ID: 27573496 RIS Download

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Associated grants

  • Agency: NHLBI NIH HHS, United States
    Id: R35 HL135775
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL136394
  • Agency: NHGRI NIH HHS, United States
    Id: U54 HG005032
  • Agency: NIDA NIH HHS, United States
    Id: R03 DA032476
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL125275
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM105404
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL112809
  • Agency: NHLBI NIH HHS, United States
    Id: T32 HL116324
  • Agency: NHLBI NIH HHS, United States
    Id: U54 HL112302
  • Agency: NHLBI NIH HHS, United States
    Id: T32 HL007917

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