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Engineering and Evolution of Synthetic Adeno-Associated Virus (AAV) Gene Therapy Vectors via DNA Family Shuffling
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Chapters
- 00:05Title
- 03:07Preparation of Plasmid Sets Encoding AAV Capsid Genes
- 04:20DNase-based Cap Gene Fragmentation
- 07:03DNA Family Shuffling
- 11:07Production of Viral Library
- 13:50Results: Screening and Selection of Individual Chimeric Capsids
- 20:00Conclusion
We demonstrate the basic technique to molecularly engineer and evolve synthetic Adeno-associated viral (AAV) gene therapy vectors via DNA family shuffling. Moreover, we provide general guidelines and representative examples for selection and analysis of individual chimeric capsids with enhanced properties on target cells in culture or in mice.
