High affinity copper binding by stefin B (cystatin B) and its role in the inhibition of amyloid fibrillation

FEBS J. 2006 Sep;273(18):4250-63. doi: 10.1111/j.1742-4658.2006.05426.x.

Abstract

We show that human stefin B, a protease inhibitor from the family of cystatins, is a copper binding protein, unlike stefin A. We have used isothermal titration calorimetry to directly monitor the binding event at pH 7 and pH 5. At pH 7 stefin B shows a picomolar affinity for copper but at pH 5 the affinity is in the nanomolar range. There is no difference in the affinity of copper between the wildtype stefin B (E31 isoform) and a variant (Y31 isoform), whereas the mutant (P79S), which is tetrameric, does not bind copper. The conformation of stefin B remains unaltered by copper binding. It is known that below pH 5 stefin B undergoes a conformational change and amyloid fibril formation. We show that copper binding inhibits the amyloid fibril formation and, to a lesser degree, the initial aggregation. Similarities to and differences from other copper binding amyloidogenic proteins are discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Amyloid / chemistry
  • Amyloid / metabolism*
  • Amyloid / ultrastructure
  • Benzothiazoles
  • Circular Dichroism
  • Copper / metabolism*
  • Cystatin B
  • Cystatins / chemistry
  • Cystatins / metabolism*
  • Fluorescence
  • Humans
  • Hydrogen-Ion Concentration
  • Microscopy, Electron, Transmission
  • Molecular Sequence Data
  • Multiprotein Complexes / chemistry*
  • Multiprotein Complexes / ultrastructure
  • Mutation
  • Protein Conformation
  • Protein Isoforms / chemistry
  • Protein Isoforms / metabolism
  • Sequence Alignment
  • Thiazoles

Substances

  • Amyloid
  • Benzothiazoles
  • CSTB protein, human
  • Cystatins
  • Multiprotein Complexes
  • Protein Isoforms
  • Thiazoles
  • thioflavin T
  • Copper
  • Cystatin B