Aptamer-based biochips for label-free detection of plant virus coat proteins by SPR imaging

被引:73
作者
Lautner, Gergely [1 ]
Balogh, Zsofia [2 ]
Bardoczy, Viola [3 ]
Meszaros, Tamas [2 ]
Gyurcsanyi, Robert E. [1 ,4 ]
机构
[1] Budapest Univ Technol & Econ, Dept Inorgan & Analyt Chem, H-1111 Budapest, Hungary
[2] Semmelweis Univ, Dept Med Chem Mol Biol & Pathobiochem, H-1094 Budapest, Hungary
[3] Budapest Univ Technol & Econ, Dept Appl Biotechnol & Food Sci, H-1111 Budapest, Hungary
[4] Hungarian Acad Sci, Res Grp Tech Analyt Chem, H-1111 Budapest, Hungary
关键词
DNA-MODIFIED SURFACES; RNA; QUANTITATION; MOLECULES; BIOSENSOR; RECOGNITION; MONOLAYERS; EVOLUTION; SEQUENCES; SELECTION;
D O I
10.1039/b922829b
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Specific detection of virus strains by affinity-based bioassays is often limited by the availability of ligands able to differentiate among close homologues of virus coat proteins. As viruses are prone to mutation, the ligand generation should, in addition, be fast enough to allow rapid identification of new varieties. These two criteria are difficult to be fulfilled by antibodies; however, they open up opportunities for aptamer-based detection. Here we report on the feasibility of selectively detecting the apple stem pitting virus (ASPV) coat proteins (PSA-H, MT32) using original DNA aptamers. Surface plasmon resonance (SPR) imaging was used together with aptamer-modified sensor chips to optimize the aptamer immobilization for highest sensitivity and to characterize the aptamer-virus coat protein binding. Different parameters affecting this binding, such as the aptamer flanking, surface coverage, and type of spacer molecules, were identified and their influence was determined. A direct label-free method is proposed for assessing the ASPV based on the detection of the respective virus coat proteins in plant extracts.
引用
收藏
页码:918 / 926
页数:9
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