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Published on: February 1, 2022
Peptide-modified electrolyte-gated organic field effect transistor. Application to Cu2+ detection
T T K Nguyen1, H V Tran2, T T Vu3
1Univ. Paris Diderot, Sorbonne Paris Cité, ITODYS, UMR 7086 CNRS, 15 rue J-A de Baïf, 75205 Paris Cedex 13, France; Department of Advanced Materials Science and Nanotechnology (AMSN), University of Science and Technology of Hanoi (USTH), Vietnam Academy of Science and Technology (VAST), 18 Hoang Quoc Viet, Nghĩa Đô, Cãu Giãy, Hanoi, Viet Nam.
This study presents a new method for detecting copper ions (Cu2+) in water using a peptide-modified transistor. This approach achieves highly sensitive and selective copper sensing with a low detection limit.
Area of Science:
- Analytical Chemistry
- Materials Science
- Biotechnology
Background:
- Accurate detection of copper ions (Cu2+) in aqueous environments is crucial for environmental monitoring and biological studies.
- Existing methods for Cu2+ detection often face challenges with selectivity, sensitivity, or complex sample preparation.
- Electrolyte-gated organic field-effect transistors (EGOFETs) offer potential for sensitive biosensing applications due to their high charge carrier mobility and low operating voltage.
Purpose of the Study:
- To develop a novel sensor for selective and sensitive detection of Cu2+ in water.
- To functionalize an EGOFET gate electrode with a Gly-Gly-His (GGH) peptide probe for Cu2+ recognition.
- To demonstrate the transduction of Cu2+ complexation into a measurable electrical signal by the GGH-functionalized EGOFET.
Main Methods:
- Immobilization of the Gly-Gly-His (GGH) peptide probe onto the EGOFET gate electrode via electrooxidation.
- Electrochemical characterization of Cu2+ complexation with the immobilized GGH probe using cyclic and square wave voltammetries.
- Electrical characterization of the GGH-functionalized EGOFET response to varying Cu2+ concentrations, monitoring threshold voltage shifts and drain current changes.
Main Results:
- Successful electrochemical evidence of Cu2+ complexation by the grafted GGH peptide.
- Demonstration that GGH-functionalized EGOFETs effectively transduce Cu2+ binding events.
- Achieved a limit of detection (LOD) of approximately 10-12 M for Cu2+.
- Observed a sensitivity of 1 µA dec-1 in the linear detection range of 10-12 M to 10-8 M.
Conclusions:
- The GGH-peptide-functionalized EGOFET is a highly sensitive and selective platform for Cu2+ detection in water.
- This approach offers a promising low-cost, label-free method for real-time monitoring of copper ions.
- The developed sensor technology has significant potential for environmental and biomedical applications requiring trace metal analysis.
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