Method for extracting and purifying adeno-associated virus and adenovirus from host cells, components and kit thereof

An adenovirus and cell technology, applied in the fields of biotechnology and medical research, can solve problems such as gradient medium health risks, cumbersome operating procedures, and reduced infection activity

Active Publication Date: 2021-10-26
贺道耀
View PDF7 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, this technique has some serious limitations in application: (1) significant reduction in infectious activity, (2) health risks associated with the gradient medium, (3) possible toxicity of the gradient medium, (4) limitations in the scale of production and (5) The operating procedures are cumbersome

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for extracting and purifying adeno-associated virus and adenovirus from host cells, components and kit thereof
  • Method for extracting and purifying adeno-associated virus and adenovirus from host cells, components and kit thereof
  • Method for extracting and purifying adeno-associated virus and adenovirus from host cells, components and kit thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0113] Example 1: Lysis, extraction and purification of adeno-associated virus and adenovirus from host cells

[0114] This example tests methods for the lysis, extraction and purification of AAV and AdV virus particles from their packaging cells (host cells). This example demonstrates that the present method achieves higher recovery and purity of virus particles compared to conventional methods. Furthermore, the method is easy to operate and can be scaled up readily.

[0115] Methods and materials

[0116] Dulbecco's modified Eagle's medium (DMEM), fetal bovine serum (FBS) and cell culture dishes were purchased from Fisher Scientific. 6-well and 12-well cell culture plates were purchased from Santa Cruz Biotechnology. Plasmid DNA Maxiprep kit was purchased from Qiagen. Lipofectamine 2000 Transduction Reagent (Transfection Reagent) was purchased from Life Technologies. DNase I, Maxima Sybr Green qPCR master mix (Master Mix, 2X), Pierce BCA protein assay kit, SDS-PAGE mini...

Embodiment 2

[0175] Embodiment 2: virus purification kit

[0176] This example tests a collection of reagents and materials, referred to as virus purification kits, for the purification of some virus particles. This example illustrates that the kit can greatly improve the quality and efficiency of virus purification.

[0177] Methods and Materials

[0178] Dulbecco's modified Eagle's medium (DMEM), fetal bovine serum (FBS) and cell culture dishes were purchased from Fisher Scientific. 6-well and 12-well cell culture plates were purchased from Santa Cruz Biotechnology. Plasmid DNA Maxiprep kit was purchased from Qiagen. Lipofectamine 2000 transduction reagent was purchased from Life Technologies. DNase I, Maxima Sybr Green qPCR master mix (2X), Pierce BCA protein assay kit, SDS-PAGE mini gels, Amicon Ultra-4 centrifugal filters and all chemicals were purchased from FisherScientific. Silica-based chromatography columns were purchased from Agilent Technologies, Inc.

[0179] cell cult...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The present invention provides a method for tertiary purification of virus particles from a sample containing host cells packaging virus particles. The three-stage purification method includes: using the first fractionation solution to precipitate and remove most of the impurity proteins; using the second fractionation solution to precipitate and collect virus particles to remove some remaining impurities; the collected virus particles are further purified by column layer The remaining impurities were removed by analysis to obtain an ultra-pure virus solution. The method also includes the steps of collecting virus host cells, cell suspending and cell lysing. This purification method is easy to operate, convenient to obtain ultra-pure virus solution with high recovery rate, suitable for large-scale and small-scale preparation, and the solution and operation steps used do not contain toxic substances to cells. Therefore, this method represents a highly desirable purification technique for vector viruses, including AAVs and adenoviruses. The present invention also includes kits or packages designed according to the above techniques.

Description

technical field [0001] The invention belongs to the field of biotechnology and medical research, and generally relates to the purification of virus particles, more specifically, to a method for extracting and purifying carrier virus particles such as adeno-associated virus and adenovirus packaged in host cells from host cells and Its components and kits. Background technique [0002] The delivery of exogenous genes and small non-coding RNAs (such as siRNA and miRNA) mediated by viral vectors is a very effective tool that is widely used in basic research and medical research and development. Viral vectors currently in use include adenovirus, retrovirus, lentivirus, adeno-associated virus (AAV), and herpes simplex virus (HSV), with retroviruses and lentiviruses being the most frequently used in recent research literature. Retroviruses and lentiviruses belong to the class of retroviruses, which are secreted in the culture medium of the host cells after packaging in the host ce...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Patents(China)
IPC IPC(8): C12N7/02
CPCC12N7/00C12N2710/10051C12N2750/14151C12N15/86C12N2710/10351
Inventor 贺道耀
Owner 贺道耀
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap