A one-pot analysis approach to simplify measurements of protein stability and folding kinetics.

Authors:
Yi-Kai Liu
Yi-Kai Liu
Leibniz University Hannover
Germany
Pin Ju Chueh
Pin Ju Chueh
Institute of Biomedical Sciences
Seattle | United States
Pei-Fen Liu
Pei-Fen Liu
Cathay General Hospital
Taiwan

Biochim Biophys Acta Proteins Proteom 2019 Mar 19;1867(3):184-193. Epub 2018 Dec 19.

Department of Food Science and Biotechnology, National Chung Hsing University, 145 Xingda Rd., South Dist., Taichung City 402, Taiwan, ROC. Electronic address:

To achieve a good understanding of the characteristics of a protein, it is important to study its stability and folding kinetics. Investigations of protein stability have been recently applied to drug-target identification, drug screening, and proteomic studies. The efficiency of the experiments performed to study protein stability and folding kinetics is now a crucial factor that needs to be optimized for these potential applications. However, the standard procedures used to carry out these experiments are usually complicated and time consuming. Large number of measurements is the bottleneck that limits the application of protein folding to large-scale experiments. To overcome this limitation, we developed a method denoted as "one-pot analysis" which is based on taking a single measurement from a mixture of samples rather than from every sample. We combined one-pot analysis with pulse proteolysis to determine the effects of the binding of maltose to maltose-binding protein on the protein folding properties. After carrying out a simple optimization, we demonstrated that protein stability or unfolding kinetics could be measured accurately with just one detection measurement. We then further applied the optimized conditions to cellular thermal shift assay (CETSA). Combining one-pot analysis with CETSA led to a successful determination of the effects of the binding of methotrexate to dihydrofolate reductase in HCT116 cancer cells. Our results demonstrated the applicability of one-pot analysis to energetics-based methods for studying protein folding. We expect the combination of one-pot analysis and energetics-based methods to significantly benefit studies such as drug-target identification, proteomic investigations, and drug screening.

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Source
http://dx.doi.org/10.1016/j.bbapap.2018.12.006DOI Listing
March 2019

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