The binding mechanism of a peptidic cyclic serine protease inhibitor

Research output: Contribution to journalJournal articleResearchpeer-review

  • Longguang Jiang
  • Anna Sigrid P. Svane
  • Hans Peter Sørensen
  • Jan K Jensen
  • Masood Hosseini
  • Zhuo Chen
  • Caroline Weydert
  • Jakob Toudahl Nielsen
  • Anni Christensen
  • Cai Yuan
  • Jensen, Knud Jørgen
  • Niels Chr Nielsen
  • Anders Malmendal
  • Mingdong Huang
  • Peter Andreasen
Serine proteases are classical objects for studies of catalytic and inhibitory mechanisms as well as interesting as therapeutic targets. Since small-molecule serine protease inhibitors generally suffer from specificity problems, peptidic inhibitors, isolated from phage-displayed peptide libraries, have attracted considerable attention. Here, we have investigated the mechanism of binding of peptidic inhibitors to serine protease targets. Our model is upain-1 (CSWRGLENHRMC), a disulfide-bond-constrained competitive inhibitor of human urokinase-type plasminogen activator with a noncanonical inhibitory mechanism and an unusually high specificity. Using a number of modified variants of upain-1, we characterised the upain-1-urokinase-type plasminogen activator complex using X-ray crystal structure analysis, determined a model of the peptide in solution by NMR spectroscopy, and analysed binding kinetics and thermodynamics by surface plasmon resonance and isothermal titration calorimetry. We found that upain-1 changes both main-chain conformation and side-chain orientations as it binds to the protease, in particular its Trp3 residue and the surrounding backbone. The properties of upain-1 are strongly influenced by the addition of three to four amino acids long N-terminal and C-terminal extensions to the core, disulfide-bond-constrained sequence: The C-terminal extension stabilises the solution structure compared to the core peptide alone, and the protease-bound structure of the peptide is stabilised by intrapeptide contacts between the N-terminal extension and the core peptide around Trp3. These results provide a uniquely detailed description of the binding of a peptidic protease inhibitor to its target and are of general importance in the development of peptidic inhibitors with high specificity and new inhibitory mechanisms.
Original languageEnglish
JournalJournal of Molecular Biology
Issue number2
Pages (from-to)235-250
Number of pages16
Publication statusPublished - 2011

    Research areas

  • Amino Acid Sequence, Humans, Molecular Sequence Data, Peptides, Cyclic, Protein Binding, Serine Proteinase Inhibitors, Surface Plasmon Resonance

ID: 37554277