Angewandte Chemie International Edition · 2022 · 20 citations · 28 references
Life SciencesBiotechnologyMolecular BiologyBiosensorsNanobiotechnologyNanotechnologyCell-nanoparticle InteractionsNanomaterial-based BiosensorsNanoparticle DesignNanosensorsQuantum DotsQuantum Dots In BiologyAntibodiesBiomolecular DetectionFörster Resonance Energy Transfer (Fret)Method Detection LimitNanomaterial-based ImmunosensorsNanoparticle-based ImmunoassaysQuantum Dot BiosensorsSemiconductor Quantum Dots
Abstract 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.
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Structural Evaluation of EGFR Inhibition Mechanisms for Nanobodies/VHH Domains
Karl R. Schmitz, Atrish Bagchi, Rob C. Roovers et al. · Structure · 2013 · 250 citations · Full text