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Structure of the AAVhu.37 capsid by cryoelectron microscopy.


ABSTRACT: Adeno-associated viruses (AAVs) are used as in vivo gene-delivery vectors in gene-therapy products and have been heavily investigated for numerous indications. Over 100 naturally occurring AAV serotypes and variants have been isolated from primate samples. Many reports have described unique properties of these variants (for instance, differences in potency, target cell or evasion of the immune response), despite high amino-acid sequence conservation. AAVhu.37 is of interest for clinical applications owing to its proficient transduction of the liver and central nervous system. The sequence identity of the AAVhu.37 VP1 to the well characterized AAVrh.10 serotype, for which no structure is available, is greater than 98%. Here, the structure of the AAVhu.37 capsid at 2.56?Å resolution obtained via single-particle cryo-electron microscopy is presented.

SUBMITTER: Kaelber JT 

PROVIDER: S-EPMC7010358 | biostudies-literature | 2020 Feb

REPOSITORIES: biostudies-literature

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Structure of the AAVhu.37 capsid by cryoelectron microscopy.

Kaelber Jason T JT   Yost Samantha A SA   Webber Keith A KA   Firlar Emre E   Liu Ye Y   Danos Olivier O   Mercer Andrew C AC  

Acta crystallographica. Section F, Structural biology communications 20200203 Pt 2


Adeno-associated viruses (AAVs) are used as in vivo gene-delivery vectors in gene-therapy products and have been heavily investigated for numerous indications. Over 100 naturally occurring AAV serotypes and variants have been isolated from primate samples. Many reports have described unique properties of these variants (for instance, differences in potency, target cell or evasion of the immune response), despite high amino-acid sequence conservation. AAVhu.37 is of interest for clinical applicat  ...[more]

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