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.</p
Overexpression of correctly folded membrane proteins is a fundamental prerequisite for functional an...
In both pro- and eukaryotes 20-30% of all genes encode alpha-helical transmembrane domain proteins, ...
The major barrier to the physical characterization and structure determination of membrane proteins ...
Overexpression of membrane proteins in Escherichia coli frequently leads to the formation of aggrega...
A major bottleneck in the characterization of membrane proteins is low yield of functional protein i...
AbstractThe overexpression of authentically folded eukaryotic membrane proteins in milligramme quant...
We describe a generic, GFP-based pipeline for membrane protein overexpression and purification in Es...
The production of recombinant membrane proteins for structural and functional studies remains techni...
Escherichia coli is one of the most widely used expression hosts for membrane proteins. However, est...
Optimizing conditions for the overexpression and purification of membrane proteins for functional an...
The production of recombinant membrane proteins for structural and functional studies remains techni...
The bacterium Escherichia coli is the most widely used expression host for overexpression trials of ...
The use of recombinant protein is a cornerstone in many structural and functional studies. The enter...
In bacteria, protein overproduction results in the formation of inclusion bodies, sized protein aggr...
Overexpression of correctly folded membrane proteins is a fundamental prerequisite for functional an...
In both pro- and eukaryotes 20-30% of all genes encode alpha-helical transmembrane domain proteins, ...
The major barrier to the physical characterization and structure determination of membrane proteins ...
Overexpression of membrane proteins in Escherichia coli frequently leads to the formation of aggrega...
A major bottleneck in the characterization of membrane proteins is low yield of functional protein i...
AbstractThe overexpression of authentically folded eukaryotic membrane proteins in milligramme quant...
We describe a generic, GFP-based pipeline for membrane protein overexpression and purification in Es...
The production of recombinant membrane proteins for structural and functional studies remains techni...
Escherichia coli is one of the most widely used expression hosts for membrane proteins. However, est...
Optimizing conditions for the overexpression and purification of membrane proteins for functional an...
The production of recombinant membrane proteins for structural and functional studies remains techni...
The bacterium Escherichia coli is the most widely used expression host for overexpression trials of ...
The use of recombinant protein is a cornerstone in many structural and functional studies. The enter...
In bacteria, protein overproduction results in the formation of inclusion bodies, sized protein aggr...
Overexpression of correctly folded membrane proteins is a fundamental prerequisite for functional an...
In both pro- and eukaryotes 20-30% of all genes encode alpha-helical transmembrane domain proteins, ...
The major barrier to the physical characterization and structure determination of membrane proteins ...