Quality control of overexpressed membrane proteins
Open Access
- 15 April 2008
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 105 (15) , 5722-5727
- https://doi.org/10.1073/pnas.0802190105
Abstract
Overexpression of membrane proteins in Escherichia coli frequently leads to the formation of aggregates or inclusion bodies, which is undesirable for most studies. Ideally, one would like to optimize the expression conditions by monitoring simultaneously and rapidly both the amounts of properly folded and aggregated membrane protein, a requirement not met by any of the currently available methods. Here, we describe a simple gel-based approach with green fluorescent protein as folding indicator to detect well folded and aggregated proteins simultaneously. The method allows for rapid screening and, importantly, pinpointing the most likely bottlenecks in protein production.Keywords
This publication has 22 references indexed in Scilit:
- Rigidity of the Subunit Interfaces of the Trimeric Glutamate Transporter GltT During TranslocationJournal of Molecular Biology, 2007
- Structure of Rat Monoamine Oxidase A and Its Specific Recognitions for Substrates and InhibitorsJournal of Molecular Biology, 2004
- Identification of the Dimer Interface of the Lactose Transport Protein from Streptococcus thermophilusJournal of Molecular Biology, 2003
- Assembly and overexpression of membrane proteins in Escherichia coliBiochimica et Biophysica Acta (BBA) - Biomembranes, 2003
- Green fluorescent protein as an indicator to monitor membrane protein overexpression in Escherichia coliFEBS Letters, 2001
- Rapid protein-folding assay using green fluorescent proteinNature Biotechnology, 1999
- Construction of a fusion protein between protein A and green fluorescent protein and its application to Western blottingFEBS Letters, 1996
- Tight regulation, modulation, and high-level expression by vectors containing the arabinose PBAD promoterJournal of Bacteriology, 1995
- Differential plasmid rescue from transgenic mouse DNAs into Escherichia coli methylation-restriction mutants.Proceedings of the National Academy of Sciences, 1990
- Host/vector interactions which affect the viability of recombinant phage lambda clonesGene, 1986