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  4. An amplified surface plasmon resonance "turn-on" sensor for mercury ion using gold nanoparticles
 
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An amplified surface plasmon resonance "turn-on" sensor for mercury ion using gold nanoparticles

Journal
Biosensors and Bioelectronics
Journal Volume
30
Journal Issue
1
Pages
235-240
Date Issued
2011
Author(s)
Chang C.-C.
Lin S.
Wei S.-C.
Chen C.-Y.
Lin C.-W.  
DOI
10.1016/j.bios.2011.09.018
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-80755153036&doi=10.1016%2fj.bios.2011.09.018&partnerID=40&md5=97fcc8664b4878e9d2885643ecab332e
https://scholars.lib.ntu.edu.tw/handle/123456789/413722
Abstract
Inorganic mercury ion (Hg(2+)) has been shown to coordinate to DNA duplexes that feature thymine-thymine (T-T) base pair mismatches. This observation suggests that an Hg(2+)-induced conformational change in a single-stranded DNA molecule can be used to detect aqueous Hg(2+). Here, we have developed an analytical method using surface plasmon resonance (SPR) to develop a highly selective and sensitive detection technique for Hg(2+) that takes advantage of T-Hg(2+)-T coordination chemistry. The general concept used in this approach is that the "turn-on" reaction of a hairpin probe via coordination of Hg(2+) by the T-T base pair results in a substantial increase in the SPR response, followed by specific hybridization with a gold nanoparticle probe to amplify the sensor performance. Meanwhile, the limit of detection is 1 nM, which is lower than other recently developed techniques. A linear correlation is observed between the measured SPR reflectivity and the logarithm of the Hg(2+) concentration over the concentration range of 5-5000 nM. Additionally, the SPR system provides high selectivity for Hg(2+) in the presence of other divalent metal ions up to micromolar concentration levels. The proposed approach is also successfully utilized for the determination of Hg(2+) in water samples.
SDGs

[SDGs]SDG6

Type
journal article

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