The small heat-shock protein αB-crystallin uses different mechanisms of chaperone action to prevent the amorphous versus fibrillar aggregation of α-lactalbumin

Biochem J. 2012 Dec 15;448(3):343-52. doi: 10.1042/BJ20121187.

Abstract

Stress conditions can destabilize proteins, promoting them to unfold and adopt intermediately folded states. Partially folded protein intermediates are unstable and prone to aggregation down off-folding pathways leading to the formation of either amorphous or amyloid fibril aggregates. The sHsp (small heat-shock protein) αB-crystallin acts as a molecular chaperone to prevent both amorphous and fibrillar protein aggregation; however, the precise molecular mechanisms behind its chaperone action are incompletely understood. To investigate whether the chaperone activity of αB-crystallin is dependent upon the form of aggregation (amorphous compared with fibrillar), bovine α-lactalbumin was developed as a model target protein that could be induced to aggregate down either off-folding pathway using comparable buffer conditions. Thus when α-lactalbumin was reduced it aggregated amorphously, whereas a reduced and carboxymethylated form aggregated to form amyloid fibrils. Using this model, αB-crystallin was shown to be a more efficient chaperone against amorphously aggregating α-lactalbumin than when it aggregated to form fibrils. Moreover, αB-crystallin forms high molecular mass complexes with α-lactalbumin to prevent its amorphous aggregation, but prevents fibril formation via weak transient interactions. Thus, the conformational stability of the protein intermediate, which is a precursor to aggregation, plays a critical role in modulating the chaperone mechanism of αB-crystallin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Heat-Shock Proteins, Small / antagonists & inhibitors
  • Heat-Shock Proteins, Small / chemistry
  • Heat-Shock Proteins, Small / metabolism
  • Humans
  • Lactalbumin / antagonists & inhibitors*
  • Lactalbumin / chemistry*
  • Molecular Chaperones / chemistry*
  • Molecular Chaperones / metabolism*
  • Protein Conformation
  • alpha-Crystallin B Chain / chemistry*
  • alpha-Crystallin B Chain / physiology*

Substances

  • Heat-Shock Proteins, Small
  • Molecular Chaperones
  • alpha-Crystallin B Chain
  • Lactalbumin