Versatile medium-throughput strategies for recombinant expression screening in structural biology

The increasing complexity of biological targets subject to structural characterization constantly demands highly versatile
approaches of recombinantly expression and purification.
When targeting macromolecular complexes, the difficulties associated to the initial recombinant screening phase are further
amplified by the need to identify suitable constructs to co-express or reconstitute in vitro the molecular interactions
essential for complex stabilization. Large industry-scale high-throughput platforms offer extremely efficient and automated
methods to obtain libraries of protein constructs for expression and purification scouting, whereas several academic
research labs still rely on more conservative "one construct, one recombinant host, one target" approaches. Frequently, the
choice depends on investments in automation, as the costs associated to creation of high-throughput facilities are not
affordable to all research groups. Aiming at minimizing time and costs associated to the initial screening for recombinant
expression; we optimized cloning and expression strategies to increase the throughput without the need of automation.
Our system consists of two major components: 1) a large library of expression vectors, based on a limited number of
commercial backbones with customized expression cassettes allowing rapid switch of combinations of expression hosts,
affinity tags and protein fusions to enhance target stability and solubility, coupled to standardized sub-cloning sites for easy
genes transfer from one expression vector to another; 2) digital tools to facilitate design of DNA constructs for expression
scouting.
In this talk, we will present the basic concepts behind the construction and functioning of our system, and we will briefly
showcase it successful usage for the identification of optimal expression constructs for various ongoing structural biology
projects in our lab, including extracellular enzymes, cytosolic macromolecular complexes, and membrane proteins.