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A Recombinant Mutant Adeno-Associated Virus and Its Related Biomaterials Efficiently Infecting Primary Microglia

A technology of microglia and biomaterials, applied in viruses, viral peptides, microorganisms, etc., can solve problems such as limiting the application of AAV

Active Publication Date: 2022-05-10
INST OF ZOOLOGY CHINESE ACAD OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

It has been confirmed that AAV-1, 2, 3, 4, 5, 7, 8, and 9 hardly infect any microglial cells in vitro and in vivo, and AAV-6 infects microglial cells in vitro with an efficiency of less than 10 %, which greatly limits the application of AAV in microglia

Method used

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  • A Recombinant Mutant Adeno-Associated Virus and Its Related Biomaterials Efficiently Infecting Primary Microglia
  • A Recombinant Mutant Adeno-Associated Virus and Its Related Biomaterials Efficiently Infecting Primary Microglia
  • A Recombinant Mutant Adeno-Associated Virus and Its Related Biomaterials Efficiently Infecting Primary Microglia

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Embodiment 1

[0045] Example 1. Construction of recombinant adeno-associated virus and analysis of its infection in primary microglial cells

[0046] 1. Packaging of recombinant adeno-associated virus (AAV)

[0047] 1. Preparation of recombinant plasmids (see figure 1 Middle A-D):

[0048] 1.1. Preparation of recombinant capsid packaging plasmid pAAV-6X

[0049] Using pAAV-RC6 as the original template, the sequence to be inserted (the underlined sequence in R) was designed on the downstream primer R, and the foreign sequence was inserted into the capsid sequence of pAAV-RC6 by PCR. Upstream primer F (nucleotide sequence is 5'-ACAGCAGCTACGCGCACA-3') and downstream primer R (nucleotide sequence is 5'-AGGCTCCCATAACATGCACATCTCCGGTCGCAGGGTCTGT CAGACGCGTCGGACCAACCGG GCTGCTGCTCTGGAGATTGAC-3′) 1 μl each (working solution concentration 10 μM), after 15 cycles, 1 μl Dpn1 enzyme was added to the PCR product to digest the original template plasmid pAAV-RC6. Afterwards, the PCR amplified product wa...

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Abstract

The invention discloses a recombinant mutant adeno-associated virus capable of efficiently infecting primary microglial cells and related biological materials. The recombinant adeno-associated virus is an adeno-associated virus expressing an AAV-6X type capsid protein, and the AAV-6X type capsid protein is a protein whose amino acid sequence is sequence 4 in the sequence table. In the present invention, the wild-type AAV-6 capsid protein is mutated as follows to obtain a mutated AAV-6 capsid protein: 7 amino acid residues are inserted between positions 588-589 of the amino acid sequence of the AAV-6 capsid protein base. The efficiency of recombinant adeno-associated virus rAAV-6X (expressing AAV-6X type capsid protein) in vitro infection of microglial cells of the present invention is higher than that of recombinant adeno-associated virus rAAV-6 (expressing wild-type AAV-6 type capsid protein) in vitro infection 8 times more efficient for microglia. The recombinant adeno-associated virus of the invention is an rAAV vector for efficiently transducing microglial cells.

Description

technical field [0001] The invention relates to the field of biotechnology, in particular to a recombinant mutant adeno-associated virus that efficiently infects primary microglial cells and related biological materials. Background technique [0002] Studies in recent years have shown that the degree of nerve damage seems to be related to the scale and activity of innate immune activity. In the central nervous system, microglia are the main immune cells and the first type of cells to respond to nerve injury, infection or pathological changes. In addition to the role of immune response, microglia play important functions such as support, nutrition, and protection in the physiological activities of neurons, and also participate in the shaping and repair of neuronal connectivity during development, and participate in neuronal synaptic plasticity processes of formation, neurogenesis, and learning. Accumulating evidence suggests that microglia-associated signaling pathways may ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N7/01C12N15/864C07K14/015C12N15/35C12R1/93
CPCC12N7/00C12N15/86C07K14/005C12N2750/14121C12N2750/14143C12N2750/14122C12N2750/14151C12N2800/107
Inventor 滕兆乾何炫程刘长梅杜洪震
Owner INST OF ZOOLOGY CHINESE ACAD OF SCI