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Coupled Assays for Monitoring Protein Refolding in Saccharomyces cerevisiae
Published on: July 9, 2013
Misfolded proteins impose a dosage-dependent fitness cost and trigger a cytosolic unfolded protein response in yeast
Kerry A Geiler-Samerotte1, Michael F Dion, Bogdan A Budnik
1Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, USA.
Abstract:
Evolving lineages face a constant intracellular threat: most new coding sequence mutations destabilize the folding of the encoded protein. Misfolded proteins form insoluble aggregates and are hypothesized to be intrinsically cytotoxic. Here, we experimentally isolate a fitness cost caused by toxicity of misfolded proteins. We exclude other costs of protein misfolding, such as loss of functional protein or attenuation of growth-limiting protein synthesis resources, by comparing growth rates of budding yeast expressing folded or misfolded variants of a gratuitous protein, YFP, at equal levels. We quantify a fitness cost that increases with misfolded protein abundance, up to as much as a 3.2% growth rate reduction when misfolded YFP represents less than 0.1% of total cellular protein. Comparable experiments on variants of the yeast gene orotidine-5'-phosphate decarboxylase (URA3) produce similar results. Quantitative proteomic measurements reveal that, within the cell, misfolded YFP induces coordinated synthesis of interacting cytosolic chaperone proteins in the absence of a wider stress response, providing evidence for an evolved modular response to misfolded proteins in the cytosol. These results underscore the distinct and evolutionarily relevant molecular threat of protein misfolding, independent of protein function. Assuming that most misfolded proteins impose similar costs, yeast cells express almost all proteins at steady-state levels sufficient to expose their encoding genes to selection against misfolding, lending credibility to the recent suggestion that such selection imposes a global constraint on molecular evolution.
Insights
Protein misfolding incurs a significant fitness cost in yeast, independent of protein function. This toxicity drives cellular evolution and impacts gene expression, even at low protein misfolding levels.
Area of Science:
- Molecular Biology
- Evolutionary Biology
- Biochemistry
Background:
- Most new protein mutations can destabilize protein folding, leading to misfolded proteins.
- Misfolded proteins aggregate and are hypothesized to be cytotoxic, posing an intracellular threat to evolving lineages.
Purpose of the Study:
- To experimentally isolate and quantify the fitness cost associated with protein misfolding toxicity.
- To investigate the cellular response to misfolded proteins and its evolutionary implications.
Main Methods:
- Comparing growth rates of budding yeast expressing folded versus misfolded variants of YFP (yellow fluorescent protein) and URA3 at equal levels.
- Quantifying fitness costs across varying abundances of misfolded proteins.
- Utilizing quantitative proteomics to analyze cellular responses, including chaperone protein synthesis.
Main Results:
- A quantifiable fitness cost increases with misfolded protein abundance, reducing growth rates by up to 3.2%.
- This cost is observed even when misfolded proteins constitute less than 0.1% of total cellular protein.
- Misfolded proteins induce a specific cytosolic chaperone response without a broader stress reaction.
Conclusions:
- Protein misfolding represents a distinct, evolutionarily relevant threat independent of protein function.
- Cellular selection against protein misfolding may impose a global constraint on molecular evolution.
- Yeast cells maintain protein expression levels that allow for selection against misfolding.
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