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Functional Trimeric SARS-CoV-2 Envelope Protein Expressed in Stable CHO Cells
Patrick Mayrhofer1, Monika Hunjadi1, Renate Kunert1
1Department of Biotechnology, Institute of Animal Cell Technology and Systems Biology, University of Natural Resources and Life Sciences (BOKU), Vienna, Austria.
Frontiers in Bioengineering and Biotechnology
|January 3, 2022
Summary
Researchers developed a method to produce high-quality recombinant SARS-CoV-2 spike proteins. This advancement is crucial for understanding virus-cell interactions and developing new COVID-19 therapies.
Area of Science:
- Virology
- Molecular Biology
- Biochemistry
Background:
- Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes the COVID-19 pandemic.
- The SARS-CoV-2 spike (S) protein mediates viral entry by binding to the ACE2 receptor.
- Existing methods for obtaining recombinant S-protein are limited, hindering research.
Purpose of the Study:
- To develop a robust protocol for recombinant expression and purification of the SARS-CoV-2 spike protein.
- To enable further studies on virus-host interactions and therapeutic development.
- To generate high-quality, full-length or trimeric spike protein variants.
Main Methods:
- Development of a recombinant Chinese Hamster Ovary (CHO) cell line.
- Stable expression of the extracellular domain of a trimeric SARS-CoV-2 spike protein variant.
- Optimization of expression and purification parameters.
Main Results:
- Successfully established a stable CHO cell line for expressing the SARS-CoV-2 spike protein.
- Identified key parameters for efficient recombinant protein production.
- Generated a trimeric variant of the spike protein's extracellular domain.
Conclusions:
- The developed protocol facilitates the production of high-quality recombinant SARS-CoV-2 spike protein.
- This resource is vital for advancing research into viral mechanisms and therapeutic strategies.
- Further studies using mutant variants can illuminate virus assembly and drug development.

