Localization of a peripheral membrane protein: Gbetagamma targets Galpha(Z)

Proc Natl Acad Sci U S A. 2000 Feb 1;97(3):1085-90. doi: 10.1073/pnas.97.3.1085.

Abstract

To explore the relative roles of protein-binding partners vs. lipid modifications in controlling membrane targeting of a typical peripheral membrane protein, Galpha(z), we directed its binding partner, betagamma, to mislocalize on mitochondria. Mislocalized betagamma directed wild-type Galpha(z) and a palmitate-lacking Galpha(z) mutant to mitochondria but did not alter localization of a Galpha(z) mutant lacking both myristate and palmitate. Thus, in this paradigm, a protein-protein interaction controls targeting of a peripheral membrane protein to the proper compartment, whereas lipid modifications stabilize interactions of proteins with membranes and with other proteins.

Publication types

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

MeSH terms

  • Amino Acid Substitution
  • Animals
  • Biological Transport
  • CHO Cells
  • Cricetinae
  • Cricetulus
  • GTP-Binding Protein alpha Subunits*
  • GTP-Binding Protein beta Subunits*
  • GTP-Binding Protein gamma Subunits*
  • GTP-Binding Proteins / metabolism*
  • Heterotrimeric GTP-Binding Proteins / genetics
  • Heterotrimeric GTP-Binding Proteins / metabolism*
  • Intracellular Membranes / metabolism*
  • MAP Kinase Signaling System
  • Membrane Lipids / metabolism
  • Membrane Proteins / metabolism*
  • Microscopy, Fluorescence
  • Mitochondria / metabolism
  • Mutagenesis, Site-Directed
  • Myristic Acid / metabolism
  • Palmitates / metabolism
  • Recombinant Fusion Proteins / metabolism
  • Transfection

Substances

  • G-protein Beta gamma
  • GTP-Binding Protein alpha Subunits
  • GTP-Binding Protein beta Subunits
  • GTP-Binding Protein gamma Subunits
  • Membrane Lipids
  • Membrane Proteins
  • Palmitates
  • Recombinant Fusion Proteins
  • Myristic Acid
  • GTP-Binding Proteins
  • Heterotrimeric GTP-Binding Proteins