4.7 Article

Yeast Synthetic Minimal Biosensors for Evaluating Protein Production

Journal

ACS SYNTHETIC BIOLOGY
Volume 10, Issue 7, Pages 1640-1650

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssynbio.0c00633

Keywords

yeast; unfolded protein response; biosensor; synthetic minimal promoter; secretion

Funding

  1. Biomolecular Discovery and Design Research Centre, Macquarie University, Sydney, Australia
  2. Centre of Excellence in Synthetic Biology - Australian Government thorough its agency, the Australian Research Council

Ask authors/readers for more resources

The unfolded protein response (UPR) is a crucial cellular response to ER stress in eukaryotic cells, with implications for human diseases and recombinant protein production. By constructing and evaluating high-throughput UPR sensors, it is possible to predict strains' protein production capacity, understand protein properties affecting secretion, and guide optimal engineering strategies for heterologous protein production.
The unfolded protein response (UPR) is a highly conserved cellular response in eukaryotic cells to counteract endoplasmic reticulum (ER) stress, typically triggered by unfolded protein accumulation. In addition to its relevance to human diseases like cancer, the induction of the UPR has a significant impact on the recombinant protein production in eukaryotic cell factories, including the industrial workhorseSaccharomyces cerevisiae. Being able to accurately detect and measure this ER stress response in single cells, enables the rapid optimization of protein production conditions and high-throughput strain selection strategies. Current methodologies to monitor the UPR in S. cerevisiae are often temporally and spatially removed from the cultivation stage or lack updated systematic evaluation. To this end, we constructed and systematically evaluated a series of high-throughput UPR sensors by different designs, incorporating either yeast native UPR promoters or novel synthetic minimal UPR promoters. The native promoters of DER1 and ERO1 were identified to have suitable UPR biosensor properties and served as an expression level guide for orthogonal sensor benchmarking. Our best synthetic minimal sensor is only 98 bp in length, has minimal homology to other native yeast sequences and displayed superior sensor characteristics. The synthetic minimal UPR sensor was able to accurately distinguish between cells expressing different heterologous proteins and between the different secretion levels of the same protein. This work demonstrated the potential of synthetic UPR biosensors as high-throughput tools to predict the protein production capacity of strains, interrogate protein properties hampering their secretion, and guide rational engineering strategies for optimal heterologous protein production.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available