4.4 Article

Novel system for detecting SARS coronavirus nucleocapsid protein using an ssDNA aptamer

Journal

JOURNAL OF BIOSCIENCE AND BIOENGINEERING
Volume 112, Issue 6, Pages 535-540

Publisher

SOC BIOSCIENCE BIOENGINEERING JAPAN
DOI: 10.1016/j.jbiosc.2011.08.014

Keywords

SARS coronavirus; nucleocapsid; aptamer; ELISA; Western blot analysis

Funding

  1. Ministry for Health, Welfare & Family Affairs, Republic of Korea [A090410]
  2. Korea Health Promotion Institute [A090410] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The outbreak of severe acute respiratory syndrome (SARS) in 2002 affected thousands of people and an efficient diagnostic system is needed for accurate detection of SARS coronavirus (SARS CoV) to prevent or limit future outbreaks. Of the several SARS Coy structural proteins, the nucleocapsid protein has been shown to be a good diagnostic marker. In this study, an ssDNA aptamer that specifically binds to SARS Coy nucleocapsid protein was isolated from a DNA library containing 45-nuceotide random sequences in the middle of an 88mer single-stranded DNA. After twelve cycles of systematic evolution of ligands by exponential enrichment (SELEX) procedure, 15 ssDNA aptamers were identified. Enzyme-linked immunosorbent assay (ELISA) analysis was then used to identify the aptamer with the highest binding affinity to the SARS Coy nucleocapsid protein. Using this approach, an ssDNA aptamer that binds to the nucleocapsid protein with a K-d of 4.93 +/- 0.30 nM was identified. Western blot analysis further demonstrated that this ssDNA aptamer could be used to efficiently detect the SARS CoV nucleocapsid protein when compared with a nucleocapsid antibody. Therefore, we believe that the selected ssDNA aptamer may be a good alternative detection probe for the rapid and sensitive detection of SARS. (C) 2011, The Society for Biotechnology, Japan. All rights reserved.

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