Preparation method, system and recombinant bacmid of recombinant adeno-associated virus
A technology for preparing a system and a virus, which is applied in the field of preparation of recombinant adeno-associated virus, can solve the problems of poor system flexibility and versatility, difficult to popularize, poor virus stability, etc., achieves flexibility and compatibility, improves passage stability, good compatibility
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[0043] The preparation method of recombinant adeno-associated virus (rAAV) provided by the invention comprises the following steps:
[0044] (1) Prepare the shuttle plasmid and its corresponding recombinant bacmid containing the baculovirus genome respectively;
[0045] The shuttle plasmid at least comprises rAAV core expression elements with heterologous functional gene fragments;
[0046] The shuttle plasmid is preferably a pFBD plasmid, which includes at least rAAV core expression elements with heterologous functional gene fragments; it may also include an expression cassette for some functional protein components required for rAAV production. The expression cassette of the functional protein component may be the expression cassette of the AAV functional protein component or the expression cassette of other functional protein components.
[0047] The recombinant bacmid containing the baculovirus genome contains expression cassettes for other functional protein components n...
Embodiment 1
[0087] Example 1. Preparation of rAAV using DH10Bac-Tn7-(ITR-GOI)-Cap-Δ(Chia-Cath)-Rep
[0088] When the shuttle plasmid pFBD contains the rAAV core expression element ITR-GOI and the AAV Cap gene expression cassette, the corresponding recombinant bacmid integrates the AAV Rep gene expression cassette and other functional protein component expression cassettes ( figure 2 A).
[0089] A preparation system for rAAV, comprising: a shuttle plasmid and its corresponding recombinant bacmid containing the baculovirus genome; the shuttle plasmid is based on the pfast.Bac.Dual plasmid, and its multiple cloning site is inserted with ITR-GOI sequence and Cap Gene, the Cap gene is placed downstream of the P10 promoter; the recombinant bacmid of the baculovirus genome is AcMNPV E2 with deletion of non-essential genes Chia gene and Cath gene, its gene sequence is as follows: Genbank accession No.KM667940.1, The Chia and Cath genes were deleted (105,353bp-108,025bp), and the Rep gene expre...
Embodiment 2
[0110] Example 2. Preparation of rAAV using DH10Bac-Tn7-(ITR-GOI)-Rep-Δ(Chia-Cath)-Cap
[0111] When the shuttle plasmid pFBD contains the core expression element ITR-GOI of rAAV and the Rep gene expression cassette of AAV, the corresponding recombinant bacmid needs to integrate the Cap gene expression cassette of AAV and the expression cassettes of other functional protein components ( image 3 A).
[0112] A preparation system for rAAV, comprising: a shuttle plasmid and its corresponding recombinant bacmid containing the baculovirus genome; the shuttle plasmid is based on the pfast.Bac.Dual plasmid, and its multiple cloning site is inserted with ITR-GOI sequence and Rep Gene, the Rep gene is placed downstream of the PH promoter; the recombinant bacmid of the baculovirus genome is AcMNPV E2 with deletion of non-essential genes Chia and Cath genes, its gene sequence is as follows: Genbank accession No.KM667940.1, its (Location range 105,353bp-108,025bp) Chia and Cath genes we...
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