Direct preparation of giant proteo-liposomes by in vitro membrane protein synthesis

J Biotechnol. 2008 Jan 20;133(2):190-5. doi: 10.1016/j.jbiotec.2007.08.023. Epub 2007 Aug 17.

Abstract

We investigated the direct constitution of membrane proteins into giant liposomes in cell-free (in vitro) protein synthesis. Giant liposomes were present in a translation reaction cocktail of a wheat germ cell-free protein translation system. Apo cytochrome b(5) (b5) and its fusion proteins were synthesized and directly localized in the liposomes. After the translation reaction, the proteo-liposomes were isolated by simplified discontinuous density-gradient centrifugation. Apo cytochrome b(5) conjugated dihydrofolate reductase (DHFR) was synthesized in the same procedure and the protein was directly displayed on the liposome surface. b5 acts as a "hydrophobic tag" for recruitment to the liposome surface.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cytochromes b5 / biosynthesis*
  • Electrophoresis, Polyacrylamide Gel
  • Green Fluorescent Proteins / metabolism
  • Liposomes / metabolism*
  • Microscopy, Fluorescence
  • Protein Biosynthesis*
  • Proteins / metabolism*
  • Tetrahydrofolate Dehydrogenase / metabolism
  • Time Factors

Substances

  • Liposomes
  • Proteins
  • enhanced green fluorescent protein
  • Green Fluorescent Proteins
  • Cytochromes b5
  • Tetrahydrofolate Dehydrogenase