Interconversion of three differentially modified and assembled forms of BiP

EMBO J. 1992 Jan;11(1):63-70.

Abstract

The immunoglobulin heavy chain binding protein BiP/GRP78 is post-translationally modified by phosphorylation and ADP ribosylation. In cells induced to synthesize higher levels of BiP, either due to the accumulation of nontransported proteins or to glucose starvation, both BiP phosphorylation and ADP ribosylation are reduced. BiP bound to other proteins is unmodified, suggesting that both phosphorylation and ADP ribosylation are restricted to the unbound BiP pool. In the present study, both modifications were further characterized in terms of their stability, the pool of BiP that harbored these modifications, and the relationship between the modified and unmodified forms of BiP. While levels of BiP synthesis vary according to the physiological state of a cell, we found that both induced and uninduced cells contain similar amounts of free BiP. However, free BiP in uninduced cells was found primarily in an aggregated state, whereas in cells that accumulate nontransported proteins, it was predominantly monomeric. Both phosphorylation and ADP ribosylation were restricted to the aggregated form of free BiP. These post-translational modifications occurred upon release of BiP from associated proteins, and could be reversed upon induction of BiP synthesis. Therefore, BiP exists either (1) complexed to other proteins, (2) as a free unmodified monomer, or (3) as free modified aggregates. Our data suggest that BiP can be interconverted from one state to another, and that the various forms are functionally distinct.

Publication types

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

MeSH terms

  • Adenosine Diphosphate / metabolism
  • Adenosine Diphosphate Ribose / metabolism
  • Animals
  • Carrier Proteins / chemistry
  • Carrier Proteins / drug effects
  • Carrier Proteins / metabolism*
  • Cell Line
  • Cycloheximide / pharmacology
  • Gene Expression Regulation
  • Glucose / deficiency
  • Heat-Shock Proteins*
  • Immunoglobulin Heavy Chains / metabolism
  • Molecular Chaperones*
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Protein Conformation
  • Protein Processing, Post-Translational*
  • Subcellular Fractions

Substances

  • Carrier Proteins
  • Heat-Shock Proteins
  • Immunoglobulin Heavy Chains
  • Molecular Chaperones
  • Phosphoproteins
  • Adenosine Diphosphate Ribose
  • Adenosine Diphosphate
  • Cycloheximide
  • Glucose
  • molecular chaperone GRP78