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Updated: Jun 1, 2026

Green Fluorescent Protein-based Expression Screening of Membrane Proteins in Escherichia coli
Published on: January 6, 2015
Cloning, expression, purification, and characterization of the membrane protein UncI from Escherichia coli
Claudia Hartmann1, Andreas Engel
1Center for Cellular Imaging and Nano Analytics, Biozentrum, University of Basel, CH-4058 Basel, Switzerland.
Abstract:
The Escherichia coli unc-operon encodes the genes for the subunits of the F0F1-ATP synthase and an integral membrane protein of unknown function called UncI. UncI influences the cell-growth and activity of F0F1, but its exact function is still unknown. The expression level is too low to extract milligram amounts of UncI from E. coli membranes and the existing purification protocol based on methanol/chloroform is not suitable for structural and functional studies. Here we present protocols to increase the expression level, to purify UncI in a detergent where UncI is monodisperse, and we characterize its oligomeric state.

