4.8 Article

A simple clickable biosensor for colorimetric detection of copper(II) ions based on unmodified gold nanoparticles

Journal

BIOSENSORS & BIOELECTRONICS
Volume 41, Issue -, Pages 663-668

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2012.09.032

Keywords

Colorimetric; Gold nanoparticles; Copper(II) ions; Click chemistry

Funding

  1. National Natural Science Foundation of China [21175036, 20907013, 21190044]
  2. Program for New Century Excellent Talents in University [NCET-10-0366]
  3. National Basic Research Program of China (973 Program) [2011CB911002, 2009CB421601]
  4. NSFHP [10JJ2005]

Ask authors/readers for more resources

A novel colorimetric copper(II) biosensor has been developed based on the high specificity of alkyne-azide click reaction to the catalysis of copper ions and unmodified gold nanoparticles (AuNPs) as the signal reporter. The clickable DNA probe consists of two parts: an azide group-modified double-stranded DNA (dsDNA) hybrid with an elongated tail and a short alkyne-modified single-stranded DNA (ssDNA). Because of low melting temperature of the short ssDNA, these two parts are separated in the absence of Cu2+. Copper ion-induced azide-alkyne click ligation caused a structural change of probe from the separated form to entire dsDNA form. This structural change of probe can be monitored by the unmodified AuNPs via mediating their aggregation with a red-to-blue colorimetric read-out because of the differential ability of ssDNA and dsDNA to protect AuNPs against salt-induced aggregation. Under the optimum conditions, this biosensor can sensitively and specifically detect Cu2+ with a low detection limit of 250 nM and a linear range of 0.5-10 mu M. The method is simple and economic without dual-labeling DNA and AuNPs modification. It is also highly selective for Cu2+ in the presence of high concentrations of other environmentally relevant metal ions because of the great specificity of the copper-caused alkyne-azide click reaction, which potentially meets the requirement of the detection in real samples. (C) 2012 Elsevier B.V. All rights reserved.

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