Chip-based detection of hepatitis C virus using RNA aptamers that specifically bind to HCV core antigen

被引:85
作者
Lee, Seram
Kim, Young Sook
Jo, Minjung
Jin, Moonsoo
Lee, Dong-ki [1 ]
Kim, Soyoun
机构
[1] Pohang Univ Sci & Technol, Dept Chem, Pohang 790784, South Korea
[2] Pohang Univ Sci & Technol, BK Sch Mol Sci, Pohang 790784, South Korea
[3] Dongguk Univ, Dept Chem, Seoul 100715, South Korea
[4] Cornell Univ, Dept Biomed Engn, Ithaca, NY 14853 USA
关键词
hepatitis C virus; SELEX; aptamers; biosensor; diagnosis;
D O I
10.1016/j.bbrc.2007.04.057
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
The development of reagents with high affinity and specificity to the antigens of hepatitis C virus (HCV) is important for the early stage diagnosis of its infection. Aptamers are short, single-stranded oligonucleotides with the ability to specifically recognize target molecules with high affinity. Herein, we report the selection of RNA aptamers that bind to the core antigen of HCV. High affinity aptamers were isolated from a 10(15) random library of 60 mer RNAs using the SELEX procedure. Importantly, the selected aptamers specifically bound to the core antigen, but not to another HCV antigen, NS5, in a protein chip-based assay. Using these aptamers, we developed an aptamer-based biosensor for HCV diagnosis and detected the core antigen from HCV infected patients' sera with good specificity. This novel aptamer-based antigen detection sensor could be applied to the early diagnosis of HCV infection. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:47 / 52
页数:6
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