4.8 Article

Peptide-coated nanotube-based biosensor for the detection of disease-specific autoantibodies in human serum

Journal

BIOSENSORS & BIOELECTRONICS
Volume 23, Issue 10, Pages 1413-1421

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2007.11.022

Keywords

carbon nanotubes; piezoelectric sensing; serum antibodies; rheumatoid arthritis-specific autoantibodies; citrullinated peptide; immunosensor

Funding

  1. NHLBI NIH HHS [N01-HV-28183, N01 HV028183, N01HV28183] Funding Source: Medline
  2. NIAID NIH HHS [R01 AI051614-05, AI050864, R01 AI051614, AI51614] Funding Source: Medline
  3. NIAMS NIH HHS [R21 AR049328] Funding Source: Medline
  4. NIDDK NIH HHS [U19 DK061934, DK61934, U19 DK061934-01] Funding Source: Medline

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We demonstrate a label-free peptide-coated carbon nanotube-based immunosensor for the direct assay of human serum. A rheumatoid arthritis (RA)-specific (cyclic citrulline-containing) peptide, was immobilized to functionalized single-walled carbon nanotubes deposited on a quartz crystal microbalance (QCM) sensing crystal. Serum from RA patients was used to probe these nanotube-based sensors, and antibody binding was detected by QCM sensing. Specific antibody binding was also determined by comparing the assay of two serum control groups (normal and diseased sera), and the native unmodified peptide. The sensitivity of the nanotube-based sensor (detection in the femtomol range) was higher than that of the established ELISA and recently described microarray assay systems, detecting 34.4 and 37.5% more RA patients with anti-citrullinated peptide antibodies than those found by ELISA and microarray, respectively. There was also an 18.4 and 19.6% greater chance of a negative test being a true indicator of a person not having RA than by either ELISA or microarray, respectively. The performance of our label-free biosensor enables its application in the direct assay of sera in research and diagnostics. (C) 2007 Elsevier B.V. All rights reserved.

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