A Nanobody-on-Quantum Dot Displacement Assay for Rapid and Sensitive Quantification of the Epidermal Growth Factor Receptor (EGFR).
Ruifang SuYu-Tang WuSofia DoulkeridouXue QiuThomas Just SørensenKimihiro SusumuIgor L MedintzPaul M P van Bergen En HenegouwenNiko HildebrandtPublished in: Angewandte Chemie (International ed. in English) (2022)
Biosensing approaches that combine small, engineered antibodies (nanobodies) with nanoparticles are often complicated. Here, we show that nanobodies with different C-terminal tags can be efficiently attached to a range of the most widely used biocompatible semiconductor quantum dots (QDs). Direct implementation into simplified assay formats was demonstrated by designing a rapid and wash-free mix-and-measure immunoassay for the epidermal growth factor receptor (EGFR). Terbium complex (Tb)-labeled hexahistidine-tagged nanobodies were specifically displaced from QD surfaces via EGFR-nanobody binding, leading to an EGFR concentration-dependent decrease of the Tb-to-QD Förster resonance energy transfer (FRET) signal. The detection limit of 80±20 pM (16±4 ng mL -1 ) was 3-fold lower than the clinical cut-off concentration for soluble EGFR and up to 10-fold lower compared to conventional sandwich FRET assays that required a pair of different nanobodies.
Keyphrases
- epidermal growth factor receptor
- energy transfer
- quantum dots
- tyrosine kinase
- advanced non small cell lung cancer
- loop mediated isothermal amplification
- sensitive detection
- high throughput
- mycobacterium tuberculosis
- small cell lung cancer
- primary care
- label free
- air pollution
- particulate matter
- computed tomography
- escherichia coli
- pseudomonas aeruginosa
- single molecule
- binding protein
- single cell
- real time pcr