TY - JOUR
T1 - Bioprocess characterization of virus-like particle production with the insect cell baculovirus expression system at nanoparticle level
AU - Puente-Massaguer, Eduard
AU - González-Domínguez, Irene
AU - Strobl, Florian
AU - Grabherr, Reingard
AU - Striedner, Gerald
AU - Lecina, Martí
AU - Gòdia, Francesc
N1 - Funding Information:
The authors thank Alois Jungbauer (University of Natural Resources and Life Sciences, Vienna, Austria) for facilitating the access to ÄKTA pure system, and Paula Alves (Instituto de Biologia Experimental e Tecnológica, Oeiras, Portugal) for providing the Hi5 cell line. We also appreciate the support of Miriam Klausberger on the protocol for Gag staining, Krisztina Koczka for providing the BV-Gag stock, Sahar Masoumeh Ghorbanpour with ELISA quantification, Martí de Cabo (Servei de Microscòpia, Universitat Autònoma de Barcelona) with cryo-TEM, Mónica Roldán (Unitat de Microscòpia Confocal, Servei d'anatomia Patològica, Institut Pediàtric de Malalties Rares, Hospital Sant Joan de Déu) with SRFM, and Jorge Fomaro and Ángel Calvache (Beckman Coulter) for facilitating the access to the CytoFlex LX. Eduard Puente-Massaguer (FPU15/03577) and Irene González-Domínguez (FPU16/02555) are recipients of FPU grants from Ministerio de Educación, Cultura y Deporte of Spain. The research group is recognized as 2017 SGR 898 by Generalitat de Catalunya.
Publisher Copyright:
© 2022 Society of Chemical Industry (SCI).
PY - 2022/9
Y1 - 2022/9
N2 - Background. Virus-like particles (VLPs) are a multivalent platform showing great promise for the development of vaccines, gene therapy, diagnostic, and drug delivery approaches. Particularly, HIV-1 Gag VLPs provide a robust and flexible scaffold for the presentation of a variety of antigens. The insect cell baculovirus expression vector system (BEVS) is nowadays one of the reference systems to produce these complex nanoparticles, but information about VLP quality, quantity, stability, as well as cell performance is scarce, especially at bioreactor scale. Results. VLPs produced in the reference High Five and Sf9 insect cell lines share similar physicochemical properties, with VLPs produced in Sf9 cells showing lower levels of double stranded DNA and protein contaminants, and a higher degree of VLP assembly. Besides VLPs, other nanoparticle populations are divergently encountered in each cell line. Hi5 supernatants contain a higher load of extracellular vesicles, while Sf9 supernatants exhibit higher concentrations of baculovirus particles. Similar titers are achieved when comparing Gag to Gag-eGFP VLP production, with the size of most of the nanoparticles produced comprised at the 150–250 nm range. Eventually, Gag VLP production in a 2 L stirred tank bioreactor is successfully demonstrated, validating bioprocess transference to the final product candidate. Conclusions. This work provides two potentially valuable strategies for the production of HIV-1 Gag VLPs and a detailed analysis of the different nanoparticle populations produced.
AB - Background. Virus-like particles (VLPs) are a multivalent platform showing great promise for the development of vaccines, gene therapy, diagnostic, and drug delivery approaches. Particularly, HIV-1 Gag VLPs provide a robust and flexible scaffold for the presentation of a variety of antigens. The insect cell baculovirus expression vector system (BEVS) is nowadays one of the reference systems to produce these complex nanoparticles, but information about VLP quality, quantity, stability, as well as cell performance is scarce, especially at bioreactor scale. Results. VLPs produced in the reference High Five and Sf9 insect cell lines share similar physicochemical properties, with VLPs produced in Sf9 cells showing lower levels of double stranded DNA and protein contaminants, and a higher degree of VLP assembly. Besides VLPs, other nanoparticle populations are divergently encountered in each cell line. Hi5 supernatants contain a higher load of extracellular vesicles, while Sf9 supernatants exhibit higher concentrations of baculovirus particles. Similar titers are achieved when comparing Gag to Gag-eGFP VLP production, with the size of most of the nanoparticles produced comprised at the 150–250 nm range. Eventually, Gag VLP production in a 2 L stirred tank bioreactor is successfully demonstrated, validating bioprocess transference to the final product candidate. Conclusions. This work provides two potentially valuable strategies for the production of HIV-1 Gag VLPs and a detailed analysis of the different nanoparticle populations produced.
KW - HIV-1
KW - baculovirus
KW - bioreactor
KW - insect cells
KW - super-resolution fluorescence microscopy
KW - virus-like particle
UR - http://www.scopus.com/inward/record.url?scp=85130978806&partnerID=8YFLogxK
U2 - 10.1002/jctb.7105
DO - 10.1002/jctb.7105
M3 - Article
AN - SCOPUS:85130978806
SN - 0268-2575
VL - 97
SP - 2456
EP - 2465
JO - Journal of Chemical Technology and Biotechnology
JF - Journal of Chemical Technology and Biotechnology
IS - 9
ER -