Abstract
Recently developed localized surface plasmon resonance (LSPR) enhanced photoelectrochemical (PEC) biosensing has emerged as a unique label-free technology owing to the high sensitivity and robust detection. Herein, a feasible PEC biosensing platform based on receptor-functionalized plasmonic Au-MoS2 nanosheets was designed for the capture of target proteins. The biomolecular interaction substantially enhances the hot electron transfer efficiency between Au and MoS2, leading to a direct change in electrocatalytic current on MoS2 as electricity readout signal. The biosensor exhibits excellent analytical performance for protein detection in a range from 41.7 nM to 4.17 μM, with a detection limit of 4.17 nM. Additionally, this system also affords real-time analysis of binding kinetics between antigen and antibody, allowing for obtaining their rate constants of association/disassociation (kon/koff) and equilibrium constant Kd of 3.95 μM. LSPR-enhanced label-free PEC monitoring system, without the participation of ultraviolet excitation and sacrifice agents, bears no harm to biomolecules and shows high-sensitivity detection, which holds great potential applications in clinical and biological analyses.
| Original language | English |
|---|---|
| Pages (from-to) | 361-369 |
| Number of pages | 9 |
| Journal | Electrochimica Acta |
| Volume | 271 |
| DOIs | |
| State | Published - 1 May 2018 |
| Externally published | Yes |
Keywords
- Antibody-antigen interaction
- Biomolecule detection
- Gold nanoparticles
- Localized surface plasmon resonance
- Molybdenum disulphide
- Photoelectrochemical biosensing