Endoplasmic reticulum chaperone GRP94 subunit assembly is regulated through a defined oligomerization domain

Biochemistry. 1996 Dec 24;35(51):16760-9. doi: 10.1021/bi962068q.

Abstract

GRP94 is an abundant, resident glycoprotein of the mammalian endoplasmic reticulum lumen and member of the hsp90 family of molecular chaperones. To identify the structure/function relationships which define the molecular basis of GRP94 activity, we have performed a structural analysis of native GRP94 and identified a discrete domain, representing amino acids 676-719, which regulates dimerization and displays autonomous oligomerization activity. Velocity sedimentation and gel filtration chromatography were used to identify native GRP94 as a dimer with an extended, rod-like shape. Limited proteolysis resulted in the loss of approximately 16 kDa from the C-terminus and disassembly into monomers, implicating the C-terminus as the site of assembly. An assembly function for the C-terminal domain was established by analysis of the quaternary structure of C-terminal constructs synthesized either in vitro or through recombinant expression. In vitro translation was used to demonstrate that a C-terminal 20 kDa domain was both necessary and sufficient for dimerization. Structural studies of recombinant fusion protein constructs yielded identification of a 44 amino acid domain that displayed autonomous dimerization activity and conferred a highly elongated structure, characteristic of native GRP94, to the fusion protein. These data, combined with molecular dimensions obtained from rotary shadowing electron microscopy, provide a structural model of GRP94 and identify the molecular basis of GRP94 self-assembly.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • Binding Sites
  • DNA Primers / genetics
  • Detergents
  • Dimerization
  • Endoplasmic Reticulum / chemistry
  • HSP70 Heat-Shock Proteins / chemistry*
  • HSP70 Heat-Shock Proteins / genetics
  • Membrane Proteins / chemistry*
  • Membrane Proteins / genetics
  • Molecular Chaperones / chemistry*
  • Molecular Chaperones / genetics
  • Molecular Structure
  • Protein Conformation
  • Recombinant Fusion Proteins / chemistry
  • Recombinant Fusion Proteins / genetics
  • Swine

Substances

  • DNA Primers
  • Detergents
  • HSP70 Heat-Shock Proteins
  • Membrane Proteins
  • Molecular Chaperones
  • Recombinant Fusion Proteins
  • glucose-regulated proteins