Abstract

The potential of luminescent semiconductor quantum dots (QDs) to enable development of hybrid inorganic-bioreceptor sensing materials has remained largely unrealized. We report the design, formation and testing of QD-protein assemblies that function as chemical sensors. In these assemblies, multiple copies of Escherichia coli maltose-binding protein (MBP) coordinate to each QD by a C-terminal oligohistidine segment and function as sugar receptors. Sensors are self-assembled in solution in a controllable manner. In one configuration, a beta-cyclodextrin-QSY9 dark quencher conjugate bound in the MBP saccharide binding site results in fluorescence resonance energy-transfer (FRET) quenching of QD photoluminescence. Added maltose displaces the beta-cyclodextrin-QSY9, and QD photoluminescence increases in a systematic manner. A second maltose sensor assembly consists of QDs coupled with Cy3-labelled MBP bound to beta-cyclodextrin-Cy3.5. In this case, the QD donor drives sensor function through a two-step FRET mechanism that overcomes inherent QD donor-acceptor distance limitations. Quantum dot-biomolecule assemblies constructed using these methods may facilitate development of new hybrid sensing materials.

Keywords

Förster resonance energy transferQuantum dotPhotoluminescenceBiosensorNanotechnologyMaltose-binding proteinBiomoleculeChemistryFluorescenceQuenching (fluorescence)Materials scienceOptoelectronicsPhysics

MeSH Terms

Biosensing TechniquesEscherichia coli ProteinsFluorescence Resonance Energy TransferMaltoseNanotechnologyPeriplasmic Binding ProteinsReproducibility of ResultsSensitivity and Specificity

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Publication Info

Year
2003
Type
article
Volume
2
Issue
9
Pages
630-638
Citations
1577
Access
Closed

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Cite This

Igor L. Medintz, Aaron R. Clapp, Hedi Mattoussi et al. (2003). Self-assembled nanoscale biosensors based on quantum dot FRET donors. Nature Materials , 2 (9) , 630-638. https://doi.org/10.1038/nmat961

Identifiers

DOI
10.1038/nmat961
PMID
12942071

Data Quality

Data completeness: 81%