Abstract

Despite many high-profile successes, recombinant membrane protein production remains a technical challenge; it is still the case that many fewer membrane protein structures have been published than those of soluble proteins. However, progress is being made because empirical methods have been developed to produce the required quantity and quality of these challenging targets. This review focuses on the microbial expression systems that are a key source of recombinant prokaryotic and eukaryotic membrane proteins for structural studies. We provide an overview of the host strains, tags and promoters that, in our experience, are most likely to yield protein suitable for structural and functional characterization. We also catalogue the detergents used for solubilization and crystallization studies of these proteins. Here, we emphasize a combination of practical methods, not necessarily high-throughput, which can be implemented in any laboratory equipped for recombinant DNA technology and microbial cell culture.

Highlights

  • Despite many high-profile successes, recombinant membrane protein production remains a technical challenge; it is still the case that many fewer membrane protein structures have been published than those of soluble proteins

  • The first structures of recombinant mammalian membrane proteins were solved in 2005 using protein that had been produced in yeast cells: the rabbit Ca2+-ATPase, SERCA1a, was produced in Saccharomyces cerevisiae [5] and the rat voltage-dependent potassium ion channel, Kv1.2 was produced in Pichia pastoris [6]

  • This review focuses on current approaches to selecting expression plasmids, microbial strains and culture conditions to enable the detergent-based purification of functional membrane proteins for biophysical characterization and crystallization trials

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Summary

Recombinant membrane protein production in microbes

Few membrane proteins are naturally abundant in their native membranes; in order to characterize them biophysically and biochemically, recombination of their genes with more efficient promoters and regulators of expression are required [1]. The first structures of recombinant mammalian membrane proteins were solved in 2005 using protein that had been produced in yeast cells: the rabbit Ca2+-ATPase, SERCA1a, was produced in Saccharomyces cerevisiae [5] and the rat voltage-dependent potassium ion channel, Kv1.2 was produced in Pichia pastoris [6]. These early results established microbes as efficient and effective host systems for synthesizing membrane proteins. Multi-drug efflux transporter (AcrB) Glycerol-3-phosphate transporter (GlpT) Lactose permease (LacY) Nitrate reductase A (NarGHI) Aquaporin (AqpZ) Ammonia channel (AmtB) Ammonia channel (AmtB). PUC515A pBAD pT7-5 pVA700 pET28b pET29b pET22b pAXH NS7 pUC515A, pET24a (2GIF) NF11 pACBH (pUC118)

Methods
An overview of microbial host usage
An overview of tag usage in microbial expression systems
C N N Oth8
C N C N NS5 N N
Promoter usage for yeast expression
Bacterial expression systems for membrane protein production
Selection of mutant T7RNAP-based expression strains for toxic genes
Expression of non-toxic or moderately-toxic target genes
Ptac-based protocols
General choices and considerations for cloning into plasmid pTTQ18
Cloning of genes encoding membrane transport proteins
Dependence of recombinant protein yields on growth and induction conditions
Yeast expression systems for membrane protein production
Saccharomyces cerevisiae
Pichia pastoris
Findings
Conclusions
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