Multiplexed site-specific electrode functionalization for multitarget biosensors

被引:15
|
作者
Levrie, Karen [1 ,2 ]
Jans, Karolien [1 ]
Vos, Rita [1 ]
Ardakanian, Niyousha [1 ]
Verellen, Niels [1 ,3 ]
Van Hoof, Chris [1 ,2 ]
Lagae, Liesbet [1 ,3 ]
Stakenborg, Tim [1 ]
机构
[1] IMEC, B-3001 Leuven, Belgium
[2] Katholieke Univ Leuven, Dept Elect Engn ESAT, B-3001 Leuven, Belgium
[3] Katholieke Univ Leuven, Dept Phys & Astron, B-3001 Leuven, Belgium
关键词
Diazonium chemistry; Electrografting; Click chemistry; Cycloaddition; Patterning; Electroaddressable immobilization; ARYL DIAZONIUM SALTS; CARBON SURFACES; CLICK CHEMISTRY; COVALENT MODIFICATION; SELECTIVE FUNCTIONALIZATION; ELECTROCHEMICAL REDUCTION; GOLD ELECTRODES; DNA; IMMOBILIZATION; MONOLAYER;
D O I
10.1016/j.bioelechem.2016.07.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Multitarget biosensors hold great promise to improve point-of-care diagnostics as they enable simultaneous detection of different biomolecular markers. Multiplexed detection of different markers, like genes, proteins, or a combination of both, propels advancement in numerous fields such as genomics, medical diagnosis and therapy monitoring. The functionalization of these biosensors, however, necessitates patterned immobilization of different bioreceptors, which remains challenging and time-consuming. We demonstrate a simple method for the patterned multiplexing of bioreceptors on a multi-electrode chip. By using the lithographically defined electrodes for surface functionalization, additional patterning steps become obsolete. Using the electrodes for self-aligned immobilization provides a spatial resolution that is limited by the electrode patterning process and that cannot be easily obtained by alternative dispensing or coating techniques. Via electrochemical reduction of diazonium salts combined with click chemistry, we achieved site-specific immobilization of two different ssDNA probes side by side on a single chip. This method was experimentally verified by cyclic voltammetry (CV), Fourier transform infrared spectroscopy (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS), and specific target recognition was visualized by fluorescence microscopy. The combination of the electroaddressability of electrografting with the chemoselectivity of click chemistry, offers a versatile platform for highly efficient site-specific functionalization of multitarget biosensors. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:61 / 66
页数:6
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