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Comprehensive mutagenesis maps the effect of all single-codon mutations in the AAV2 rep gene on AAV production.
Jain, Nina K; Ogden, Pierce J; Church, George M.
Afiliação
  • Jain NK; Wyss Institute for Biologically Inspired Engineering, Boston, United States.
  • Ogden PJ; Department of Genetics, Harvard Medical School, Boston, United States.
  • Church GM; Wyss Institute for Biologically Inspired Engineering, Boston, United States.
Elife ; 122024 Mar 27.
Article em En | MEDLINE | ID: mdl-38536879
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas do Capsídeo / Vetores Genéticos Idioma: En Revista: Elife Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas do Capsídeo / Vetores Genéticos Idioma: En Revista: Elife Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido