Abstract
Recombinant adeno-associated viruses (rAAVs) are the predominant gene therapy vector. Several rAAV vectored therapies have achieved regulatory approval, but production of sufficient rAAV quantities remains difficult. The AAV Rep proteins, which are essential for genome replication and packaging, represent a promising engineering target for improvement of rAAV production but remain underexplored. To gain a comprehensive understanding of the Rep proteins and their mutational landscape, we assayed the effects of all 39,297 possible single codon mutations to the AAV2 rep gene on AAV2 production. Most beneficial variants are not observed in nature, indicating that improved production may require synthetic mutations. Additionally, the effects of AAV2 rep mutations were largely consistent across capsid serotypes, suggesting that production benefits are capsid independent. Our results provide a detailed sequence-to-function map that enhances our understanding of Rep protein function and lays the groundwork for Rep engineering and enhancement of large scale gene therapy production.
Competing Interest Statement
A full list of GMC's tech transfer, advisory roles, and funding sources can be found on the lab's website: http://arep.med.harvard.edu/gmc/tech.html. Harvard University has filed a patent application for inventions related to this work.
Footnotes
Email addresses: Nina: ninajain{at}g.harvard.edu, Pierce: pierce.ogden{at}gmail.com, George: gchurch{at}genetics.med.harvard.edu
Figures 5A and 5C and accompanying discussion revised; Table S2 added to accompany Figure S8; Acknowledgements updated; GitHub and GEO links added; minor formatting changes
https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE226265