Serpin latency transition at atomic resolution

Proc Natl Acad Sci U S A. 2014 Oct 28;111(43):15414-9. doi: 10.1073/pnas.1407528111. Epub 2014 Oct 13.

Abstract

Protease inhibition by serpins requires a large conformational transition from an active, metastable state to an inactive, stable state. Similar reactions can also occur in the absence of proteases, and these latency transitions take hours, making their time scales many orders of magnitude larger than are currently accessible using conventional molecular dynamics simulations. Using a variational path sampling algorithm, we simulated the entire serpin active-to-latent transition in all-atom detail with a physically realistic force field using a standard computing cluster. These simulations provide a unifying picture explaining existing experimental data for the latency transition of the serpin plasminogen activator inhibitor-1 (PAI-1). They predict a long-lived intermediate that resembles a previously proposed, partially loop-inserted, prelatent state; correctly predict the effects of PAI-1 mutations on the kinetics; and provide a potential means to identify ligands able to accelerate the latency transition. Interestingly, although all of the simulated PAI-1 variants readily access the prelatent intermediate, this conformation is not populated in the active-to-latent transition of another serpin, α1-antitrypsin, which does not readily go latent. Thus, these simulations also help elucidate why some inhibitory serpin families are more conformationally labile than others.

Keywords: conformational change; molecular simulations; plasminogen activator inhibitor-1.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amino Acid Sequence
  • Azetidines / chemistry
  • Azetidines / pharmacology
  • Kinetics
  • Models, Molecular*
  • Molecular Sequence Data
  • Plasminogen Activator Inhibitor 1 / chemistry
  • Protein Binding / drug effects
  • Protein Structure, Secondary
  • Pyrimidinones / chemistry
  • Pyrimidinones / pharmacology
  • Serpins / chemistry*
  • Thermodynamics

Substances

  • AZ3976
  • Azetidines
  • Plasminogen Activator Inhibitor 1
  • Pyrimidinones
  • Serpins