Elucidation of the binding interaction interface between AAV serotype 11 capsid protein and host nuclear import proteins
Adeno-associated viruses (AAVs) are widely acknowledged as versatile vectors for gene therapy due to their non-pathogenic nature, inherent capacity for tissue-specific targeting, and their potential for customizable engineering. The N terminus of the AAV capsid protein VP1 plays a pivotal role in gu...
Gardado en:
| Principais autores: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Elsevier
2025-12-01
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| Series: | Molecular Therapy: Methods & Clinical Development |
| Assuntos: | |
| Acceso en liña: | http://www.sciencedirect.com/science/article/pii/S2329050125002256 |
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