4.5 Article

Graphene Bioelectronic Nose for the Detection of Odorants with Human Olfactory Receptor 2AG1

期刊

CHEMOSENSORS
卷 9, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/chemosensors9070174

关键词

real-time; sensor; pi-pi stacking; drop-cast; carbon surfaces; resistor; passivated; MVD; non-covalent

资金

  1. European Social Fund via the Welsh Government [c80816]
  2. Engineering and Physical Sciences Research Council [EP/S02252X/1]
  3. Knowledge Economy Skills Scholarships (KESS), Innovate UK [102877]
  4. European Regional Development Fund via the Welsh Government
  5. European Regional Development Fund via the Welsh Governments Smart Expertise Operation
  6. Innovate UK [011971]
  7. SPTS Technologies Ltd.
  8. Pegasus Chemicals Ltd.

向作者/读者索取更多资源

A real-time sensor utilizing a graphene resistor immobilized with OR2AG1 receptor for detecting amyl butyrate has been demonstrated. The sensor showed high sensitivity and selectivity towards the target odorant, with a linear sensor response between 0.1-500 pM and a sensitivity as low as 500 fM. The approach provides an alternative sensing platform for bioelectronic nose applications.
A real-time sensor for the detection of amyl butyrate (AB) utilising human olfactory receptor 2AG1 (OR2AG1), a G-protein coupled receptor (GPCR) consisting of seven transmembrane domains, immobilized onto a graphene resistor is demonstrated. Using CVD graphene as the sensor platform, allows greater potential for more sensitive detection than similar sensors based on carbon nanotubes, gold or graphene oxide platforms. A specific graphene resistor sensor was fabricated and modified via non-covalent pi-pi stacking of 1,5 diaminonaphthalene (DAN) onto the graphene channel, and subsequent anchoring of the OR2AG1 receptor to the DAN molecule using glutaraldehyde coupling. Binding between the target odorant, amyl butyrate, and the OR2AG1 receptor protein generated a change in resistance of the graphene resistor sensor. The functionalized graphene resistor sensors exhibited a linear sensor response between 0.1-500 pM and high selectively towards amyl butyrate, with a sensitivity as low as 500 fM, whilst control measurements using non-specific esters, produced a negligible sensor response. The approach described here provides an alternative sensing platform that can be used in bioelectronic nose applications.

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