A sensitive diagnostic assay of rheumatoid arthritis using three-dimensional ZnO nanorod structure

Keum Young Ahn, Koochul Kwon, Junghwan Huh, Gyu Tae Kim, Eun Bong Lee, Donghyun Park, Jeewon Lee

Research output: Contribution to journalArticlepeer-review

25 Citations (Scopus)

Abstract

We synthesized a three-dimensional nanorod structure of zinc oxide (ZnO) using a simple sol-gel process and systematically investigated properties of the ZnO nanorods regarding protein adsorption and effect on fluorescence emission. As compared to conventional polystyrene plate that has been widely used for strong protein adsorption, the ZnO nanorods had a superior protein adsorption capacity and significantly amplified fluorescence emission, suggesting the ZnO nanorods are attractive for fluorescence-based biomolecular detection assays. When applied to diagnostic assay of rheumatoid arthritis (RA) using cyclic citrullinated peptide (CCP) probe with a RCGRS motif that reportedly has a strong affinity for ZnO, the ZnO nanorods gave apparently high positive signals for all the RA-positive standards and patient sera, whereas upon the detection using conventional polystyrene plate, all the detection signals were relatively negligible. Moreover, the streptavidin-mediated immobilization of well oriented CCP further enhanced sensitivity, even for a 5000-times diluted patient serum. A highly sensitive detection of a very small amount of RA autoantibodies is important because individuals at high risk of developing RA can be identified several years before the clinical onset. Consequently, the fluorescence-based sensitive assay of RA was successfully performed using the three-dimensional ZnO nanorods, owing to the fluorescence amplification and protein/peptide adsorption properties and dimensionality of ZnO nanorods that in turn increases probe accessibility to anti-CCP RA autoantibodies. Although RA was assayed here for proof-of-concept, the ZnO nanorods-based assay can be applied in general to sensitive detection of a wide variety of antibody or protein targets.

Original languageEnglish
Pages (from-to)378-385
Number of pages8
JournalBiosensors and Bioelectronics
Volume28
Issue number1
DOIs
Publication statusPublished - 2011 Oct 15

Bibliographical note

Funding Information:
This study was supported by t he National Research Laboratory Project (grant no. 2010-0018908 , the main project that supported this work), the Microbial Genomics and Applications Center at KRIBB (grant no. 2010-K000599 ), the Basic Science Research Program (ERC program, grant no. 2010-0029409 ) of the National Research Foundation of Korea (NRF) grant, and the Public welfare & Safety research program (grant no. 2010-0020778 ) funded by the Korea government. This work was also supported by the Seoul R&BD Program (grant no. PA100026M0211612 ) and the National Research Foundation of Korea (NRF) (grant no. 2010-0027771 ). Appendix A

Keywords

  • Diagnostic assay
  • Fluorescence
  • Proteins
  • Rheumatoid arthritis
  • Sensitivity
  • ZnO nanorods

ASJC Scopus subject areas

  • Biotechnology
  • Biophysics
  • Biomedical Engineering
  • Electrochemistry

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