Dynamic Allostery Modulates Catalytic Activity by Modifying the Hydrogen Bonding Network in the Catalytic Site of Human Pin1

Molecules. 2017 Jun 15;22(6):992. doi: 10.3390/molecules22060992.

Abstract

Allosteric communication among domains in modular proteins consisting of flexibly linked domains with complimentary roles remains poorly understood. To understand how complementary domains communicate, we have studied human Pin1, a representative modular protein with two domains mutually tethered by a flexible linker: a WW domain for substrate recognition and a peptidyl-prolyl isomerase (PPIase) domain. Previous studies of Pin1 showed that physical contact between the domains causes dynamic allostery by reducing conformation dynamics in the catalytic domain, which compensates for the entropy costs of substrate binding to the catalytic site and thus increases catalytic activity. In this study, the S138A mutant PPIase domain, a mutation that mimics the structural impact of the interdomain contact, was demonstrated to display dynamic allostery by rigidification of the α2-α3 loop that harbors the key catalytic residue C113. The reduced dynamics of the α2-α3 loop stabilizes the C113-H59 hydrogen bond in the hydrogen-bonding network of the catalytic site. The stabilized hydrogen bond between C113 and H59 retards initiation of isomerization, which explains the reduced isomerization rate by ~20% caused by the S138A mutation. These results provide new insight into the interdomain allosteric communication of Pin1.

Keywords: H/D exchange; NMR; dynamic allostery; human Pin1; hydrogen bond; spin relaxation; structure dynamics.

MeSH terms

  • Binding Sites
  • Catalytic Domain
  • Histidine / chemistry
  • Humans
  • Hydrogen Bonding
  • Isomerism
  • Magnetic Resonance Spectroscopy
  • Mutation
  • NIMA-Interacting Peptidylprolyl Isomerase / chemistry*
  • NIMA-Interacting Peptidylprolyl Isomerase / genetics
  • NIMA-Interacting Peptidylprolyl Isomerase / metabolism*
  • Protein Binding
  • Protein Conformation
  • Protein Structure, Tertiary

Substances

  • NIMA-Interacting Peptidylprolyl Isomerase
  • Histidine
  • PIN1 protein, human