TY - JOUR
T1 - Insect Cells for High-Yield Production of SARS-CoV-2 Spike Protein
T2 - Building a Virosome-Based COVID-19 Vaccine Candidate
AU - Fernandes, Bárbara
AU - Castro, Rute
AU - Bhoelan, Farien
AU - Bemelman, Denzel
AU - Gomes, Ricardo A.
AU - Costa, Júlia
AU - Gomes-Alves, Patrícia
AU - Stegmann, Toon
AU - Amacker, Mario
AU - Alves, Paula M.
AU - Fleury, Sylvain
AU - Roldão, António
N1 - Funding Information:
Funding: This research was funded by the European Union’s Horizon 2020 research and innovation pro-gramme under grant agreement N◦ 730964 (project “TRANSVAC2”) and N◦ 951668 (project “TRANSVAC-DS”). Funding from the INTERFACE Programme, through the Innovation, Tech-nology and Circular Economy Fund (FITEC), iNOVA4Health—UIDB/04462/2020 and UIDP/04462/2020, a program financially supported by Fundação para a Ciência e Tecnologia (FCT)/Ministério da Ciência, Tecnologia e Ensino Superior, and by FCT through the initiatives “Investigador FCT” Program (IF/01704/2014), Exploratory Research and Development Projects (EXPL/BBB-BIO/1541/2013 and IF/01704/2014/CP1229/CT0001), and PhD fellowship (SFRH/BD/138937/2018).
Funding Information:
Acknowledgments: This work was supported by the European Union’s Horizon 2020 research and innovation programme under grant agreement N◦ 730964 (project “TRANSVAC2”) and N◦ 951668 (project “TRANSVAC-DS”). Funding from the INTERFACE Programme, through the Innovation, Technology and Circular Economy Fund (FITEC), iNOVA4Health—UIDB/04462/2020 and UIDP/04462/2020, a program financially supported by Fundação para a Ciência e Tecnologia (FCT)/Ministério da Ciência, Tecnologia e Ensino Superior, and by FCT through the initiatives “Inves-tigador FCT” Program (IF/01704/2014), Exploratory Research and Development Projects (EXPL/BBB-BIO/1541/2013 and IF/01704/2014/CP1229/CT0001), and PhD fellowship (SFRH/BD/138937/2018) is gratefully acknowledged. MS data were collected at UniMS—MassSpectrometry Unit team (ITQB NOVA/iBET, Oeiras, Portugal).
Funding Information:
This research was funded by the European Union?s Horizon 2020 research and innovation programme under grant agreement N? 730964 (project ?TRANSVAC2?) and N? 951668 (project ?TRANSVAC-DS?). Funding from the INTERFACE Programme, through the Innovation, Technology and Circular Economy Fund (FITEC), iNOVA4Health?UIDB/04462/2020 and UIDP/04462/2020, a program financially supported by Funda??o para a Ci?ncia e Tecnologia (FCT)/Minist?rio da Ci?ncia, Tecnologia e Ensino Superior, and by FCT through the initiatives ?Investigador FCT? Program (IF/01704/2014), Exploratory Research and Development Projects (EXPL/BBB-BIO/1541/2013 and IF/01704/2014/CP1229/CT0001), and PhD fellowship (SFRH/BD/138937/2018).
Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/4
Y1 - 2022/4
N2 - The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) homotrimeric spike (S) protein is responsible for mediating host cell entry by binding to the angiotensin-converting enzyme 2 (ACE2) receptor, thus being a key viral antigen to target in a coronavirus disease 19 (COVID-19) vaccine. Despite the availability of COVID-19 vaccines, low vaccine coverage as well as unvaccinated and immune compromised subjects are contributing to the emergence of SARS-CoV-2 variants of concern. Therefore, continued development of novel and/or updated vaccines is essential for protecting against such new variants. In this study, we developed a scalable bioprocess using the insect cells-baculovirus expression vector system (IC-BEVS) to produce high-quality S protein, stabilized in its pre-fusion conformation, for inclusion in a virosome-based COVID-19 vaccine candidate. By exploring different bioprocess engineering strategies (i.e., signal peptides, baculovirus transfer vectors, cell lines, infection strategies and formulation buffers), we were able to obtain ~4 mg/L of purified S protein, which, to the best of our knowledge, is the highest value achieved to date using insect cells. In addition, the insect cell-derived S protein exhibited glycan processing similar to mammalian cells and mid-term stability upon storage (up to 90 days at −80 and 4◦C or after 5 freeze-thaw cycles). Noteworthy, antigenicity of S protein, either as single antigen or displayed on the surface of virosomes, was confirmed by ELISA, with binding of ACE2 receptor, pan-SARS antibody CR3022 and neutralizing antibodies to the various epitope clusters on the S protein. Binding capacity was also maintained on virosomes-S stored at 4◦C for 1 month. This work demonstrates the potential of using IC-BEVS to produce the highly glycosylated and complex S protein, without compromising its integrity and antigenicity, to be included in a virosome-based COVID-19 vaccine candidate.
AB - The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) homotrimeric spike (S) protein is responsible for mediating host cell entry by binding to the angiotensin-converting enzyme 2 (ACE2) receptor, thus being a key viral antigen to target in a coronavirus disease 19 (COVID-19) vaccine. Despite the availability of COVID-19 vaccines, low vaccine coverage as well as unvaccinated and immune compromised subjects are contributing to the emergence of SARS-CoV-2 variants of concern. Therefore, continued development of novel and/or updated vaccines is essential for protecting against such new variants. In this study, we developed a scalable bioprocess using the insect cells-baculovirus expression vector system (IC-BEVS) to produce high-quality S protein, stabilized in its pre-fusion conformation, for inclusion in a virosome-based COVID-19 vaccine candidate. By exploring different bioprocess engineering strategies (i.e., signal peptides, baculovirus transfer vectors, cell lines, infection strategies and formulation buffers), we were able to obtain ~4 mg/L of purified S protein, which, to the best of our knowledge, is the highest value achieved to date using insect cells. In addition, the insect cell-derived S protein exhibited glycan processing similar to mammalian cells and mid-term stability upon storage (up to 90 days at −80 and 4◦C or after 5 freeze-thaw cycles). Noteworthy, antigenicity of S protein, either as single antigen or displayed on the surface of virosomes, was confirmed by ELISA, with binding of ACE2 receptor, pan-SARS antibody CR3022 and neutralizing antibodies to the various epitope clusters on the S protein. Binding capacity was also maintained on virosomes-S stored at 4◦C for 1 month. This work demonstrates the potential of using IC-BEVS to produce the highly glycosylated and complex S protein, without compromising its integrity and antigenicity, to be included in a virosome-based COVID-19 vaccine candidate.
KW - IC-BEVS
KW - protein production
KW - spike protein
KW - virosomes
UR - https://www.scopus.com/pages/publications/85128739659
U2 - 10.3390/pharmaceutics14040854
DO - 10.3390/pharmaceutics14040854
M3 - Article
AN - SCOPUS:85128739659
SN - 1999-4923
VL - 14
JO - Pharmaceutics
JF - Pharmaceutics
IS - 4
M1 - 854
ER -