Impact of Adeno‐Associated Virus Production on Capsid Heterogeneity and Product Quality
Adeno-associated virus (AAV) capsids are inherently heterogeneous, arising from viral protein stoichiometric assembly, post-translational modifications, genome packaging, and manufacturing process conditions. Understanding how AAV manufacturing processes affect capsid heterogeneity and corresponding drug product quality impact is essential for AAV-based gene therapies. We investigated the effects of extended production duration and capsid localization at harvest on capsid heterogeneity. Analytical characterization revealed that prolonged production increased extracellular AAV concentrations but also elevated the proportion of empty capsids, overall hydrophobicity, and deamidation of viral protein (VP). These changes altered charge-dependent separation during anion exchange chromatography (AEX). Capsids derived from intracellular fractions showed even higher levels of deamidation and empty particles compared to extracellular populations, further impacting AEX purification performance. Collectively, these findings demonstrate that both production time and capsid localization significantly influence AAV purification process performance and critical quality attributes. Process control strategies to minimize capsid heterogeneity are consequently critical to ensure a consistent quality profile in AAV manufacturing.
Authors
- Sarah Laughlin (ORCID: https://orcid.org/0000-0002-3783-7205)
- Evan DaSilva
- Rob Horton
- Thomas Thiers
- Luke Mustich
- Eli Wiberg
- Rudenc Lushi (ORCID: https://orcid.org/0009-0004-6893-0738)
- Jin Yin (ORCID: https://orcid.org/0000-0001-5315-1265)
- Alex Meola
- Ify Iwuchukwu
- David Rouleau
- Richa Jaiswal
- Matt Perez
- Brian Brazell
- Eugenia Fandunyan
- Michael Mercaldi
- Qi Zhang
- Ben Rogers
- James McGivney
- Xiaotong Fu
- Yongseok Kim
Institutions
- Oxford BioMedica (United Kingdom) (GB)
Publication Details
- Journal
- Biotechnology and Bioengineering
- Published
- 2026-05-02
- DOI
- https://doi.org/10.1002/bit.70219
- Primary Topic
- Protein purification and stability
- Type
- article
- Field-Weighted Citation Impact
- 0.00