Fusion Domains Guide the Oriented Insertion of Light-Driven Proton Pumps into Liposomes

Biophys J. 2017 Sep 19;113(6):1181-1186. doi: 10.1016/j.bpj.2017.06.022. Epub 2017 Jul 8.

Abstract

One major objective of synthetic biology is the bottom-up assembly of minimalistic nanocells consisting of lipid or polymer vesicles as architectural scaffolds and of membrane and soluble proteins as functional elements. However, there is no reliable method to orient membrane proteins reconstituted into vesicles. Here, we introduce a simple approach to orient the insertion of the light-driven proton pump proteorhodopsin (PR) into liposomes. To this end, we engineered red or green fluorescent proteins to the N- or C-terminus of PR, respectively. The fluorescent proteins optically identified the PR constructs and guided the insertion of PR into liposomes with the unoccupied terminal end facing inward. Using the PR constructs, we generated proton gradients across the vesicle membrane along predefined directions such as are required to power (bio)chemical processes in nanocells. Our approach may be adapted to direct the insertion of other membrane proteins into vesicles.

Publication types

  • Letter

MeSH terms

  • Cryoelectron Microscopy
  • Electrophoresis, Polyacrylamide Gel
  • Escherichia coli
  • Green Fluorescent Proteins / genetics
  • Light*
  • Liposomes / chemistry*
  • Luminescent Proteins / genetics
  • Membrane Potentials
  • Optical Imaging
  • Phosphatidylcholines
  • Protein Domains
  • Proton Pumps / chemistry*
  • Proton Pumps / genetics
  • Protons
  • Recombinant Fusion Proteins / chemistry
  • Red Fluorescent Protein
  • Rhodopsins, Microbial / genetics
  • Rhodopsins, Microbial / metabolism*

Substances

  • Liposomes
  • Luminescent Proteins
  • Phosphatidylcholines
  • Proton Pumps
  • Protons
  • Recombinant Fusion Proteins
  • Rhodopsins, Microbial
  • proteorhodopsin
  • Green Fluorescent Proteins
  • 1,2-oleoylphosphatidylcholine