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

被引:64
作者
Chen, Longyan [1 ,2 ]
Wei, Hongping [1 ]
Guo, Yongchao [1 ]
Cui, Zongqiang [1 ]
Zhang, Zhiping [1 ]
Zhang, Xian-En [1 ]
机构
[1] Chinese Acad Sci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Hubei, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
基金
美国国家科学基金会;
关键词
Hantaan virus nucleocapsid protein; Gold nanoparticle; Immuno-PCR; POLYMERASE-CHAIN-REACTION; BARCODE AMPLIFICATION ASSAY; HANTAVIRUS INFECTIONS; HEMORRHAGIC-FEVER; RENAL SYNDROME; SEROLOGICAL ASSAYS; SURFACE COVERAGE; RT-PCR; ANTIGEN; SENSITIVITY;
D O I
10.1016/j.jim.2009.05.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 similar to 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. (c) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:64 / 70
页数:7
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