High-throughput analysis of mumps virus and the virus-specific monoclonal antibody on the arrays of a cationic polyelectrolyte with a spectral SPR biosensor

被引:17
作者
Kim, Hyun-Soo
Jung, Se-Hui
Kim, Sang-Hyun
Suh, In-Bum
Kim, Woo Jin
Jung, Jae-Wan
Yuk, Jong seol
Kim, Young-Myeong
Ha, Kwon-Soo [1 ]
机构
[1] Kangwon Natl Univ, Coll Med, Dept Mol & Cellular Biochem, Chunchon 200701, Kangwon Do, South Korea
[2] Kangwon Natl Univ, Coll Med, Dept Microbiol, Chunchon 200701, Kangwon Do, South Korea
[3] Kangwon Natl Univ, Coll Med, Dept Lab Med, Chunchon 200701, Kangwon Do, South Korea
[4] Kangwon Natl Univ, Coll Med, Dept Internal Med, Chunchon 200701, Kangwon Do, South Korea
关键词
mumps virus; PDDA; proteinarrays; serodiagnosis; SPR biosensor;
D O I
10.1002/pmic.200600432
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We investigated the potential use of a spectral surface plasmon resonance (SPR) biosensor in a high-throughput analysis of mumps virus and a mumps virus-specific mAb on the arrays of a cationic polyelectrolyte, poly(diallyldimethylammonium chloride) (PDDA). The PDDA surface was constructed by electrostatic adsorption of the polyelectrolyte onto a monolayer of 11-mercaptoundecanoic acid (MUA). Poly-L-lysine was also adsorbed onto the MUA monolayer and compared with the PDDA surface in the capacity of mumps virus immobilization. The PDDA surface showed a higher adsorption of mumps virus than the poly-L-lysine surface. The SPR signal caused by the virus binding onto the PDDA surface was proportional to the concentration of mumps virus from 0.5 x 10(5) to 14 x 10(5) pfu/mL. The surface structure of the virus arrays was visualized by atomic force microscopy. Then, a dose-dependent increase in the SPR signal was observed when various concentrations of the antimumps virus antibody in buffer or human serum were applied to the virus arrays, and their interaction was specific. Thus, it is likely that the spectral SPR biosensor based on the cationic polyelectrolyte surface may provide an efficient system for a high-throughput analysis of intact virus and serodiagnosis of infectious diseases.
引用
收藏
页码:6426 / 6432
页数:7
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