Peptide ligands for the affinity purification of adeno-associated viruses from HEK 293 cell lysates
W. Chu, E. Barbieri, R. Prodromou, P. Greback-Clarke, W. K. Smith, B. D. Moore, R. E. Kilgore, C. L. Cummings, J. Pancorbo, G. L. Gilleskie, M. A. Daniele, S. Menegatti
Abstract
Adeno-associated viruses (AAVs) are the vector of choice for delivering gene therapies that can cure inherited and acquired diseases. Clinical research on various AAV serotypes significantly increased in recent years alongside regulatory approvals of AAV-based therapies. The current AAV purification platform hinges on the capture step, for which several affinity resins are commercially available. These adsorbents rely on protein ligands - typically camelid antibodies - that provide high binding capacity and selectivity, but suffer from low biochemical stability and high cost, and impose harsh elution conditions (pH 1013 vp per mL of resin) and product yields ([~]50-80%) on par with commercial adsorbents. The peptide-based adsorbents were finally utilized to purify AAV2 from a HEK 293 cell lysate, affording high recovery (50-80%), 80-to-400-fold reduction of host cell proteins (HCPs), and high transduction activity (up to 80%) of the purified viruses.
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