Cargando…
Targeting AAV vectors to the central nervous system by engineering capsid–receptor interactions that enable crossing of the blood–brain barrier
Viruses have evolved the ability to bind and enter cells through interactions with a wide variety of cell macromolecules. We engineered peptide-modified adeno-associated virus (AAV) capsids that transduce the brain through the introduction of de novo interactions with 2 proteins expressed on the mou...
Autores principales: | Huang, Qin, Chen, Albert T., Chan, Ken Y., Sorensen, Hikari, Barry, Andrew J., Azari, Bahar, Zheng, Qingxia, Beddow, Thomas, Zhao, Binhui, Tobey, Isabelle G., Moncada-Reid, Cynthia, Eid, Fatma-Elzahraa, Walkey, Christopher J., Ljungberg, M. Cecilia, Lagor, William R., Heaney, Jason D., Chan, Yujia A., Deverman, Benjamin E. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10355383/ https://www.ncbi.nlm.nih.gov/pubmed/37467291 http://dx.doi.org/10.1371/journal.pbio.3002112 |
Ejemplares similares
-
Delivering genes across the blood-brain barrier: LY6A, a novel cellular receptor for AAV-PHP.B capsids
por: Huang, Qin, et al.
Publicado: (2019) -
A High-Efficiency AAV for Endothelial Cell Transduction Throughout the Central Nervous System
por: Krolak, Trevor, et al.
Publicado: (2022) -
Efficient Recombinase-Mediated Cassette Exchange in hPSCs to Study the Hepatocyte Lineage Reveals AAVS1 Locus-Mediated Transgene Inhibition
por: Ordovás, Laura, et al.
Publicado: (2015) -
AAV capsid CD8+ T-cell epitopes are highly conserved across AAV serotypes
por: Hui, Daniel J, et al.
Publicado: (2015) -
Tailoring the AAV2 capsid vector for bone-targeting
por: Alméciga-Díaz, Carlos J., et al.
Publicado: (2018)