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An improved anion-exchange HPLC method for the detection and purification of adenoviral particles
- Source :
- Gene Therapy. 7:1055-1062
- Publication Year :
- 2000
- Publisher :
- Springer Science and Business Media LLC, 2000.
-
Abstract
- We have developed an anion-exchange high-performance liquid chromatography (HPLC) method using Q Sepharose XL (Amersham Pharmacia Biotech) as adsorbent to analyze samples containing adenovirus. This method has several major advantages over the HPLC method previously described for quantitating particles, namely (1) a >10-fold improvement in the detection limit of adenovirus in crude preparations; (2) absence of interferences originating from nucleic acids and proteins which usually contaminate crude samples; (3) unprecedented sharpness and symmetry of adenovirus peak, rendering the identification of the viral peak unambiguous, even in extremely crude and dilute preparations; and (4) no enzymatic treatment required even for crude samples. This assay was used to quantitate particles in samples taken at the transfection and amplification stages of production of various recombinant adenovirus, and in cultures of wild-type adenovirus of different serotypes. A modification of this analytical method was also developed for the purification of infectious adenovirus particles, including fiber-modified and third-generation recombinant viruses, giving highly purified preparations from low-titer crude lysates with an excellent overall recovery (50-74%).
- Subjects :
- viruses
Genetic Vectors
Biology
Transfection
medicine.disease_cause
Recombinant virus
High-performance liquid chromatography
Adenoviridae
Cell Line
law.invention
Sepharose
law
Genetics
medicine
Humans
Serotyping
Molecular Biology
Chromatography, High Pressure Liquid
Detection limit
Chromatography
Ion exchange
Molecular biology
Nucleic acid
Recombinant DNA
Molecular Medicine
Subjects
Details
- ISSN :
- 14765462 and 09697128
- Volume :
- 7
- Database :
- OpenAIRE
- Journal :
- Gene Therapy
- Accession number :
- edsair.doi.dedup.....19c8331e84cee93dc5414925a0ebd4b1
- Full Text :
- https://doi.org/10.1038/sj.gt.3301190