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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
Open publication

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Fully functional AAV viral vectors with highly altered structural cores and subunit interfaces using ProteinMPNNDOI 10.1101/2025.07.24.666527
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