Article
Fully functional AAV viral vectors with highly altered structural cores and subunit interfaces using ProteinMPNN
2025-07-26
Abstract excerpt
Adeno-associated viruses (AAV) have emerged as a viable vector for gene therapy, with several clinical approvals and a growing pipeline in clinical trials. These vectors have several challenges that need to be addressed to widen their use, including improving tropisms, reducing manufacturing costs, increasing storage stability, minimising their immunogenicity, or evasion of existing AAV immunity in which neutralis...
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Identifiers and source
- Literature Corpus work
- 1bf5edf4-013c-5066-9533-cf6d990f9c5e
- DOI
- 10.1101/2025.07.24.666527
