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DOI 10.1016/j.jim.2009.05.007

Медицинская библиотека · Journal of immunological methods · 2009

Gold nanoparticle enhanced immuno-PCR for ultrasensitive detection of Hantaan virus nucleocapsid protein.

Chen Longyan, Wei Hongping, Guo Yongchao, Cui Zongqiang, Zhang Zhiping, Zhang Xian-En

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

A functionalized gold nanoparticle (GNP) enhanced ultrasensitive immuno-PCR assay (GNP-IPCR on ELISA plate), which was modified from the recent developed bio-barcode assay (BCA) technique, was developed to detect Hantaan virus nucleocapsid protein (HNP). During the assay, the target antigen HNP was captured by a polyclonal antibody coated on ELISA microplate wells, followed by adding GNP dually modified with oligonucleotides and a HNP specific monoclonal antibody L13 (mAb L13) to form a sandwich immuno-complex. The oligonucleotides on the GNP contained two strands: one as capture DNA immobilized on the surface of the GNP through Au-S bond and the other as signal amplification DNA, which was partially complementary with the capture DNA. After the immuno-complex was formed, the signal DNA was released by heating, and consequently characterized by PCR/gel electrophoresis and SYBR-Green real time PCR. The detection limit of this method could reach down to 10 fg/mL for detecting purified HNP in buffers as well as in human serum, which was approximately 7 orders of magnitude more sensitive than that of conventional ELISA. The current assay format might be adopted for other proteins that need ultra-high sensitive detection.

Для цитирования: Chen Longyan, Wei Hongping, Guo Yongchao, Cui Zongqiang, Zhang Zhiping, Zhang Xian-En. Gold nanoparticle enhanced immuno-PCR for ultrasensitive detection of Hantaan virus nucleocapsid protein.. Journal of immunological methods. 2009. DOI: 10.1016/j.jim.2009.05.007.

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