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作者:

Xiansong, Wang (Xiansong, Wang.) | Yi, Sun (Yi, Sun.) | Shan, Jing (Shan, Jing.) | Xuemet, Ma (Xuemet, Ma.) | Yi, Zeng (Yi, Zeng.)

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EI Scopus

摘要:

We have improved real-time immuno-PCR (IPCR) with nanoparticle based amplification. Gold magnetic particles were functionalized with antibodies against the HIV capsid protein p24 and gold nanoparticles were functionalized with both oligonucleotide barcodes and antibodies against a nonoverlapping region of the cognate p24. In the presence of p24, the gold magnetic particles and the gold nanoparticles form sandwiched structures that are magnetically separated from mixture. After dehybridization of the barcode DNA on the gold nanoparticle, the released barcodes are quickly identified by realtime PCR. The limit of detection was 100 copies of p24 antigens. Results show that the real-time IPCR through nanoparticle based barcode amplification offers an disruptive approach to p24 detection and quantification, thus may potentially shorten the window of HIV-I diagnosis, and might be valuable to monitor the response to anti-retroviral treatment when RNA copy number is very below. © 2007 Crown Copyright.

关键词:

Antigens Computer aided diagnosis DNA Immunology Nanobiotechnology Oligonucleotides Viruses

作者机构:

  • [ 1 ] [Xiansong, Wang]College of Life Science and Bioengineering, Beijing University of Technology, Beijing, China
  • [ 2 ] [Yi, Sun]College of Life Science and Bioengineering, Beijing University of Technology, Beijing, China
  • [ 3 ] [Shan, Jing]College of Life Science and Bioengineering, Beijing University of Technology, Beijing, China
  • [ 4 ] [Xuemet, Ma]College of Life Science and Bioengineering, Beijing University of Technology, Beijing, China
  • [ 5 ] [Yi, Zeng]College of Life Science and Bioengineering, Beijing University of Technology, Beijing, China
  • [ 6 ] [Yi, Zeng]Chinese Center for Disease Control and Prevention, Beijing, China

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年份: 2007

页码: 1198-1201

语种: 英文

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SCOPUS被引频次: 8

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