Universal Real-Time PCR-Based Assay for Lentiviral Titration

被引:59
作者
Barczak, Wojciech [1 ,2 ]
Suchorska, Wiktoria [1 ]
Rubis, Blazej [3 ]
Kulcenty, Katarzyna [4 ,5 ]
机构
[1] Greater Poland Canc Ctr, Radiobiol Lab, Dept Med Phys, PL-61866 Poznan, Poland
[2] Poznan Univ Med Sci, Dept Head & Neck Surg, Greater Poland Canc Ctr, Poznan, Poland
[3] Poznan Univ Med Sci, Dept Clin Chem & Mol Diagnost, PL-60355 Poznan, Poland
[4] Poznan Univ Med Sci, Dept Canc Immunol, Chair Med Biotechnol, Poznan, Poland
[5] Greater Poland Canc Ctr, Gene Therapy Lab, Dept Canc Immunol, PL-61866 Poznan, Poland
关键词
Lentivirus; qPCR; Titration methods; WPRE; Albumin; POLYMERASE-CHAIN-REACTION; GENE-TRANSFER; DNA; EXPRESSION; VECTORS; TITER;
D O I
10.1007/s12033-014-9815-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lentiviral vectors are efficient vehicles for stable gene transfer in both dividing and non-dividing cells. This feature among others makes lentiviral vectors a powerful tool in molecular research. However, the use of lentiviruses in research studies and clinical trials requires a precise and validated titration method. In this study, we describe a qPCR-based approach for estimation of lentiviral vector titer (pLV-THM-GFP). The use of WPRE (Woodchuck Hepatitis Virus Posttranscriptional Regulatory Element) and albumin genes as templates for an SYBR green-based real-time qPCR method allows for a rapid, sensitive, reproducible, and accurate assessment of lentiviral copy number at an integrated lentiviral DNA level. Furthermore, this optimization enables measurement of lentiviral concentration even in very poor quality and small quantity material. Consequently, this approach provides researchers with a tool to perform low-cost assessment with highly repeatable results.
引用
收藏
页码:195 / 200
页数:6
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