S-Click Reaction for Isotropic Orientation of Oxidases on Electrodes to Promote Electron Transfer at Low Potentials.
Lin XiaMing-Jie HanLu ZhouAiping HuangZhaoya YangTianyuan WangFahui LiLu YuChanglin TianZhongsheng ZangQing-Zheng YangChenli LiuWenxu HongYi LuLital AlfontaJiangyun WangPublished in: Angewandte Chemie (International ed. in English) (2019)
Electrochemical sensors are essential for point-of-care testing (POCT) and wearable sensing devices. Establishing an efficient electron transfer route between redox enzymes and electrodes is key for converting enzyme-catalyzed reactions into electrochemical signals, and for the development of robust, sensitive, and selective biosensors. We demonstrate that the site-specific incorporation of a novel synthetic amino acid (2-amino-3-(4-mercaptophenyl)propanoic acid) into redox enzymes, followed by an S-click reaction to wire the enzyme to the electrode, facilitates electron transfer. The fabricated biosensor demonstrated real-time and selective monitoring of tryptophan (Trp) in blood and sweat samples, with a linear range of 0.02-0.8 mm. Further developments along this route may result in dramatic expansion of portable electrochemical sensors for diverse health-determination molecules.
Keyphrases
- electron transfer
- low cost
- gold nanoparticles
- label free
- amino acid
- carbon nanotubes
- molecularly imprinted
- reduced graphene oxide
- healthcare
- public health
- solid state
- mental health
- solid phase extraction
- sensitive detection
- heart rate
- room temperature
- blood pressure
- risk assessment
- mass spectrometry
- ionic liquid
- health promotion
- simultaneous determination