Improve Research Reproducibility A Bio-protocol resource
Peer-reviewed
tooltip

Virus Binding and Internalization Assay for Adeno-associated Virus

腺相关病毒的病毒结合和内化测定实验

GB Garrett E. Berry
Longping V. Tse Longping V. Tse

发布: 2017年01月20日第7卷第2期 DOI: 10.21769/BioProtoc.2110 浏览次数: 13276

评审: Yanjie LiAngela CoronaKristin Shingler

download pdf PDF PDF
ask Q&A
引用
收藏
Cited by

参见作者原研究论文

The authors used this protocol in:

Cover of The Journal of Biological Chemistry, featuring study using the protocol.

Jan 2016

Advertisement

Special Issue on Protocols for Organoid Research
Technologies for RNA Detection
“科研可重复性与创新”系列网络研讨会
Presubmission Inquiry

实验方案合集

专注于特定技术或应用的、详细的、经过同行评审的实验方案合集

Cancer Research
Immunology
Developmental Biology
Microbiology
Neuroscience
Cell Imaging - A Special Collection for Cell Bio 2023
查看更多 more

相关实验方案

生物流体中细胞外DNA的分离和定量

生物流体中细胞外DNA的分离和定量

Ľubica Janovičová [...] Peter Celec

2020年08月20日 5268 阅读

端粒染色体外环的扩增和定量

端粒染色体外环的扩增和定量

Nathaniel J. Robinson and William P. Schiemann

2023年03月05日 2444 阅读

胃液 DNA 的内镜下采集与分析：用于发现肿瘤生物标志物的液体活检方法

胃液 DNA 的内镜下采集与分析：用于发现肿瘤生物标志物的液体活检方法

Francine Carla Cadoná [...] Emmanuel Dias-Neto

2026年09月05日 97 阅读

Abstract

The binding and internalization of adeno-associated virus (AAV) is an important determinant of viral infectivity and tropism. The ability to dissect these two tightly connected cellular processes would allow better understanding and provide insight on virus entry and trafficking. In the following protocol, we describe a quantitative PCR (qPCR) based method to determine the amount of vector bound to the cell surface and the amount of subsequent virus internalization based on viral genome quantification. This protocol is optimized for studying AAV. Nevertheless, it can serve as a backbone for studying other viruses with careful modification.

Keywords: Adeno-associated virus (腺相关病毒) search Binding (结合) search Internalization (内化) search Virus entry (病毒进入) search Virus (病毒) search Cell surface (细胞表面) search

Background

Studies that assess AAV biology generally use transgene expression as the experimental endpoint. However, there are a number of critical steps AAV must successfully navigate before it reaches the nucleus and transduces the cell. Therefore, there are multiple distinct steps in the AAV infectious pathway that could be disrupted individually or collectively, leading to altered transduction. Assessment of AAV binding and internalization are important first steps in determining the cause of transduction differences observed upon cellular modification by small molecules, CRISPR-based gene knockout, siRNA-based gene knockdown, or other experimental procedures.

Materials and Reagents

  1. 12-well tissue culture (TC) treated plates (Corning, catalog number: 3513 )
  2. GeneMate 1.7 ml microcentrifuge tubes (BioExpress, catalog number: C-3262-1 )
  3. Tips  
  4. Lightcycler 96-well qPCR plates (Roche Molecular Systems, catalog number: 04729692001 )
  5. Cell lifter (Corning, catalog number: 3008 )
  6. HeLa cells (ATCC, catalog number: CCL-2 )
  7. Purified single-stranded AAV (any serotype) (Grieger et al., 2012)
  8. 1x PBS (Thermo Fisher Scientific, GibcoTM, catalog number: 14190144 )
  9. DNeasy Blood and Tissue Kit (QIAGEN, catalog number: 69504 )
  10. Molecular grade water (Mediatech, catalog number: 46-000-C )
  11. DMEM (Thermo Fisher Scientific, GibcoTM, catalog number: 11995065 )
  12. Trypsin-EDTA (Thermo Fisher Scientific, GibcoTM, catalog number: 25300054 )
  13. Fetal bovine serum (FBS) (Sigma-Aldrich, catalog number: F2442 )
  14. 100x penicillin/streptomycin (Thermo Fisher Scientific, GibcoTM, catalog number: 15140122 )
  15. FastStart Essential DNA Green Master Mix (Roche Molecular Systems, catalog number: 06402712001 )
  16. Virus-specific qPCR primers (at a working concentration of 20 µM each)
    1. fLuc-F – AAAAGCACTCTGATTGACAAATAC
    2. fLuc-R – CCTTCGCTTCAAAAAATGGAAC
  17. Human genomic qPCR primers (at a working concentration of 20 µM each)
    1. hLB2C1-F – GTTAACAGTCAGGCGCATGGGCC
    2. hLB2C1-R – CCATCAGGGTCACCTCTGGTTCC
  18. 10 ng/μl CBA-fLuc plasmid stock solution (see Recipes)
  19. 100 ng/μl HeLa genomic DNA stock solution (see Recipes)

Equipment

  1. Pipette 
  2. Biosafety cabinet
  3. CO2 tissue culture incubator (NuAire, model number: NU-5500 )
  4. Tabletop centrifuge (Eppendorf, catalog number: 022620401 )
  5. Lightcycler 96 qPCR instrument (Roche Molecular Systems, catalog number: 05815916001 )
  6. PCR plate microcentrifuge (VWR, catalog number: 89184-608 )

Procedure

English
中文翻译

文章信息

版权信息

© 2017 The Authors; exclusive licensee Bio-protocol LLC.

如何引用

Readers should cite both the Bio-protocol article and the original research article where this protocol was used:

  1. Berry, G. E. and Tse, L. V. (2017). Virus Binding and Internalization Assay for Adeno-associated Virus. Bio-protocol 7(2): e2110. DOI: 10.21769/BioProtoc.2110.
  2. Berry, G. E. and Asokan, A. (2016). Chemical modulation of endocytic sorting augments adeno-associated viral transduction. J Biol Chem 291(2): 939-947.

    3. ris ris Download Citation in RIS Format

分类

免疫学 > 补体分析 > 病毒

分子生物学 > DNA > DNA 定量

您对这篇实验方案有问题吗？

在此处发布您的问题，我们将邀请本文作者来回答。同时，我们会将您的问题发布到Bio-protocol Exchange，以便寻求社区成员的帮助。

post 发布问题
0 Q&A
pen 提交稿件