95. Incorporation of AAV Serotype 2 Viral Protein 2 into Other AAV Serotype Capsids
Daniel Zhang, Jun Li, Yinglu Feng, Adam Snowden, Georgy Aslanidi, Nicholas Muzyczka, Arun Srivastava, Changquan Ling, Chen Ling
Abstract
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Daniel Zhang, Jun Li, Yinglu Feng, Adam Snowden, Georgy Aslanidi, Nicholas Muzyczka, Arun Srivastava, Changquan Ling, Chen Ling
Abstract
Open-access reader
It was previously documented that large ligands inserted after residue 138 in the adeno-associated virus serotype 2 (AAV2) viral protein 2 (VP2) is tolerant to produce nearly wild-type levels of recombinant AAV2 (rAAV2) vectors (J Virol. 78(12):6595-609, 2004). Furthermore, insertion of enhanced green fluorescent protein (EGFP) into VP2 resulted in a rAAV2 particle, whose trafficking could be temporally monitored using confocal microscopy. Here, we examined whether AAV2 VP2 (2VP2) could be incorporated into other AAV serotype capsids during viral production.
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It was previously documented that large ligands inserted after residue 138 in the adeno-associated virus serotype 2 (AAV2) viral protein 2 (VP2) is tolerant to produce nearly wild-type levels of recombinant AAV2 (rAAV2) vectors (J Virol. 78(12):6595-609, 2004). Furthermore, insertion of enhanced green fluorescent protein (EGFP) into VP2 resulted in a rAAV2 particle, whose trafficking could be temporally monitored using confocal microscopy. Here, we examined whether AAV2 VP2 (2VP2) could be incorporated into other AAV serotype capsids during viral production.
Key concepts: Plasmid, Capsid, Green fluorescent protein, Molecular biology, Biology, Virology, Recombinant DNA, Adeno-associated virus