Particle concentration measurement of virus samples using electrospray differential mobility analysis and quantitative amino acid analysis

被引:18
作者
Cole, Kenneth D. [1 ]
Pease, Leonard F., III [2 ]
Tsai, De-Hao [1 ]
Singh, Tania [1 ]
Lute, Scott [3 ]
Brorson, Kurt A. [3 ]
Wang, Lili [1 ]
机构
[1] NIST, Chem Sci & Technol Lab, Gaithersburg, MD 20899 USA
[2] Univ Utah, Dept Chem Engn, Salt Lake City, UT 84112 USA
[3] FDA, CDER, Div Monoclonal Antibodies, Silver Spring, MD 20903 USA
关键词
Electrospray; Differential mobility analysis; Amino acid analysis; Virus concentration; FIELD-FLOW FRACTIONATION; PCR; BACTERIOPHAGE-MS2; PROTEIN; SCATTERING; COMPLEXES; SYSTEM; ASSAYS; PHAGE; RNA;
D O I
10.1016/j.chroma.2009.05.083
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Virus reference materials are needed to develop and calibrate detection devices and instruments. We used electrospray differential mobility analysis (ES-DMA) and quantitative amino acid analysis (AAA) to determine the particle concentration of three small model viruses (bacteriophages MS2, PP7, and phi X174). The biological activity, purity, and aggregation of the virus samples were measured using plaque assays, denaturing gel electrophoresis, and size-exclusion chromatography. ES-DMA was developed to count the virus particles using gold nanoparticles as internal standards. ES-DMA additionally provides quantitative measurement of the size and extent of aggregation in the virus samples. Quantitative AAA was also used to determine the mass of the viral proteins in the pure virus samples. The samples were hydrolyzed and the masses of the well-recovered amino acids were used to calculate the equivalent concentration of vital particles in the samples. The concentration of the virus samples determined by ES-DMA was in good agreement with the concentration predicted by AAA for these purified samples. The advantages and limitations of ES-DMA and AAA to characterize virus reference materials are discussed. Published by Elsevier B.V.
引用
收藏
页码:5715 / 5722
页数:8
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