TY - JOUR
T1 - Bioanalytics for Influenza Virus-Like Particle Characterization and Process Monitoring
AU - Carvalho, Sofia B.
AU - Silva, Ricardo J.S.
AU - Sousa, Marcos F.Q.
AU - Peixoto, Cristina
AU - Roldão, António
AU - Carrondo, Manuel J.T.
AU - Alves, Paula M.
N1 - Funding Information:
This work was funded by Fundação para a Ciência e Tecnologia (FCT, Portugal) through the following initiatives: PhD fellowship SFRH/BD/52302/2013 MolBioS Program (SC), Post-Doctoral fellowship SFRH/BPD/121558/2016 (RS), “Investigador FCT” Program (IF/01704/2014) (AR), and Exploratory Research and Development Projects (EXPL/BBB-BIO/1541/2013 and IF/ 01704/2014/CP1229/CT0001) (AR). This work was also supported by EU-funded project “EDUFLUVAC” (FP7-HEALTH-2013-INNOVATION−1, GA n. 602640). iNOVA4Health (UIDB/04462/2020, and UIDP/04462/2020), a program financially supported by Fundação para a Ciência e Tecnologia / Ministério da Educação e Ciência, through national funds is acknowledged. Funding from Programa INTERFACE, through Fundo de Inovação, Tecnologia e Economia Circular (FITEC), is gratefully acknowledged.
Publisher Copyright:
Copyright © 2022 Carvalho, Silva, Sousa, Peixoto, Roldão, Carrondo and Alves.
PY - 2022/2/18
Y1 - 2022/2/18
N2 - Virus-like particles (VLPs) are excellent platforms for the development of influenza vaccine candidates. Nonetheless, their characterization is challenging due to VLPs’ unique biophysical and biochemical properties. To cope with such complexity, multiple analytical techniques have been developed to date (e.g., single-particle analysis, thermal stability, or quantification assays), most of which are rarely used or have been successfully demonstrated for being applicable for virus particle characterization. In this study, several biophysical and biochemical methods have been evaluated for thorough characterization of monovalent and pentavalent influenza VLPs from diverse groups (A and B) and subtypes (H1 and H3) produced in insect cells using the baculovirus expression vector system (IC-BEVS). Particle size distribution and purity profiles were monitored during the purification process using two complementary technologies — nanoparticle tracking analysis (NTA) and tunable resistive pulse sensing (TRPS). VLP surface charge at the selected process pH was also assessed by this last technique. The morphology of the VLP (size, shape, and presence of hemagglutinin spikes) was evaluated using transmission electron microscopy. Circular dichroism was used to assess VLPs’ thermal stability. Total protein, DNA, and baculovirus content were also assessed. All VLPs analyzed exhibited similar size ranges (90–115 nm for NTA and 129–141 nm for TRPS), surface charges (average of −20.4 mV), and morphology (pleomorphic particles resembling influenza virus) exhibiting the presence of HA molecules (spikes) uniformly displayed on M1 protein scaffold. Our data shows that HA titers and purification efficiency in terms of impurity removal and thermal stability were observed to be particle dependent. This study shows robustness and generic applicability of the tools and methods evaluated, independent of VLP valency and group/subtype. Thus, they are most valuable to assist process development and enhance product characterization.
AB - Virus-like particles (VLPs) are excellent platforms for the development of influenza vaccine candidates. Nonetheless, their characterization is challenging due to VLPs’ unique biophysical and biochemical properties. To cope with such complexity, multiple analytical techniques have been developed to date (e.g., single-particle analysis, thermal stability, or quantification assays), most of which are rarely used or have been successfully demonstrated for being applicable for virus particle characterization. In this study, several biophysical and biochemical methods have been evaluated for thorough characterization of monovalent and pentavalent influenza VLPs from diverse groups (A and B) and subtypes (H1 and H3) produced in insect cells using the baculovirus expression vector system (IC-BEVS). Particle size distribution and purity profiles were monitored during the purification process using two complementary technologies — nanoparticle tracking analysis (NTA) and tunable resistive pulse sensing (TRPS). VLP surface charge at the selected process pH was also assessed by this last technique. The morphology of the VLP (size, shape, and presence of hemagglutinin spikes) was evaluated using transmission electron microscopy. Circular dichroism was used to assess VLPs’ thermal stability. Total protein, DNA, and baculovirus content were also assessed. All VLPs analyzed exhibited similar size ranges (90–115 nm for NTA and 129–141 nm for TRPS), surface charges (average of −20.4 mV), and morphology (pleomorphic particles resembling influenza virus) exhibiting the presence of HA molecules (spikes) uniformly displayed on M1 protein scaffold. Our data shows that HA titers and purification efficiency in terms of impurity removal and thermal stability were observed to be particle dependent. This study shows robustness and generic applicability of the tools and methods evaluated, independent of VLP valency and group/subtype. Thus, they are most valuable to assist process development and enhance product characterization.
KW - analytical tools
KW - biochemical characterization
KW - biophysical characterization
KW - bioprocess monitoring
KW - influenza
KW - vaccines
KW - virus-like particles
UR - http://www.scopus.com/inward/record.url?scp=85125852030&partnerID=8YFLogxK
U2 - 10.3389/fbioe.2022.805176
DO - 10.3389/fbioe.2022.805176
M3 - Article
AN - SCOPUS:85125852030
SN - 2296-4185
VL - 10
JO - Frontiers in Bioengineering and Biotechnology
JF - Frontiers in Bioengineering and Biotechnology
M1 - 805176
ER -