A secondary C1s interaction site on C1-inhibitor is essential for formation of a stable enzyme-inhibitor complex

FEBS Lett. 1997 Mar 17;405(1):42-6. doi: 10.1016/s0014-5793(96)01529-3.

Abstract

This paper examines the location of a secondary binding site for C1s on C1-inhibitor (C1-inh) which is required for the formation of SDS-stable Cls-C1-inh complexes. We used a synthetic peptide (residues 448-459) corresponding to the distal hinge region of C1-inh. This peptide binds to C1s and C1s preincubated with the peptide cleaves C1-inh but does not form a stable C1s-C1-inh complex. Computer modelling of C1-inh shows that residues Q452, Q453 and F455 are surface-exposed and that the secondary binding site may also include residues H291 and F292 which are conserved in serpins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites
  • Complement C1 / chemistry
  • Complement C1 / metabolism*
  • Complement C1 Inactivator Proteins / chemistry
  • Complement C1 Inactivator Proteins / metabolism*
  • Computer Graphics
  • Humans
  • Models, Molecular
  • Peptides / metabolism
  • Protein Conformation

Substances

  • Complement C1
  • Complement C1 Inactivator Proteins
  • Peptides