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Status: Bibliographieeintrag

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Verfasst von:Große, Stefanie [VerfasserIn]   i
 Börner, Kathleen [VerfasserIn]   i
 Fakhiri, Julia [VerfasserIn]   i
 Laketa, Vibor [VerfasserIn]   i
 Wiedtke, Ellen [VerfasserIn]   i
 Gunkel, Manuel [VerfasserIn]   i
 Grimm, Dirk [VerfasserIn]   i
Titel:Relevance of assembly-activating protein for adeno-associated virus vector production and capsid protein stability in mammalian and insect cells
Verf.angabe:Stefanie Grosse, Magalie Penaud-Budloo, Anne-Kathrin Herrmann, Kathleen Börner, Julia Fakhiri, Vibor Laketa, Chiara Krämer, Ellen Wiedtke, Manuel Gunkel, Lucie Ménard, Eduard Ayuso, Dirk Grimm
Jahr:2017
Umfang:20 S.
Fussnoten:Posted online 2 August 2017 ; Gesehen am 08.06.2018
Titel Quelle:Enthalten in: Journal of virology
Ort Quelle:Baltimore, Md. : Soc., 1967
Jahr Quelle:2017
Band/Heft Quelle:91(2017,20) Artikel-Nummer e01198-17, 20 Seiten
ISSN Quelle:1098-5514
Abstract:The discovery that adeno-associated virus 2 (AAV2) encodes an eighth protein, called assembly-activating protein (AAP), transformed our understanding of wild-type AAV biology. Concurrently, it raised questions about the role of AAP during production of recombinant vectors based on natural or molecularly engineered AAV capsids. Here, we show that AAP is indeed essential for generation of functional recombinant AAV2 vectors in both mammalian and insect cell-based vector production systems. Surprisingly, we observed that AAV2 capsid proteins VP1 to -3 are unstable in the absence of AAP2, likely due to rapid proteasomal degradation. Inhibition of the proteasome led to an increase of intracellular VP1 to -3 but neither triggered assembly of functional capsids nor promoted nuclear localization of the capsid proteins. Together, this underscores the crucial and unique role of AAP in the AAV life cycle, where it rapidly chaperones capsid assembly, thus preventing degradation of free capsid proteins. An expanded analysis comprising nine alternative AAV serotypes (1, 3 to 9, and rh10) showed that vector production always depends on the presence of AAP, with the exceptions of AAV4 and AAV5, which exhibited AAP-independent, albeit low-level, particle assembly. Interestingly, AAPs from all 10 serotypes could cross-complement AAP-depleted helper plasmids during vector production, despite there being distinct intracellular AAP localization patterns. These were most pronounced for AAP4 and AAP5, congruent with their inability to rescue an AAV2/AAP2 knockout. We conclude that AAP is key for assembly of genuine capsids from at least 10 different AAV serotypes, which has implications for vectors derived from wild-type or synthetic AAV capsids. IMPORTANCE: Assembly of adeno-associated virus 2 (AAV2) is regulated by the assembly-activating protein (AAP), whose open reading frame overlaps with that of the viral capsid proteins. As the majority of evidence was obtained using virus-like particles composed solely of the major capsid protein VP3, AAP's role in and relevance for assembly of genuine AAV capsids have remained largely unclear. Thus, we established a trans-complementation assay permitting assessment of AAP functionality during production of recombinant vectors based on complete AAV capsids and derived from any serotype. We find that AAP is indeed a critical factor not only for AAV2, but also for generation of vectors derived from nine other AAV serotypes. Moreover, we identify a new role of AAP in maintaining capsid protein stability in mammalian and insect cells. Thereby, our study expands our current understanding of AAV/AAP biology, and it concomitantly provides insights into the importance of AAP for AAV vector production.
DOI:doi:10.1128/JVI.01198-17
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Kostenfrei: Volltext ; Verlag: http://dx.doi.org/10.1128/JVI.01198-17
 Kostenfrei: Volltext: http://jvi.asm.org/content/91/20/e01198-17
 DOI: https://doi.org/10.1128/JVI.01198-17
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:AAP
 AAV
 adeno-associated virus
 assembly-activating protein
 capsid assembly
 parvovirus
K10plus-PPN:1576200760
Verknüpfungen:→ Zeitschrift

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