2008
DOI: 10.1016/j.snb.2008.05.018
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Development of an optical biosensor using gold nanoparticles and quantum dots for the detection of Porcine Reproductive and Respiratory Syndrome Virus

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Cited by 58 publications
(50 citation statements)
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“…There are hosts of biomolecular interactions/processes that are studied using QD energy transfer formats and these include nucleic acid interactions, binding protein conformation changes, antibody binding, aptamer interactions, and protease cleavage [283,513,[515][516][517][518]524,554]. Assay formats found in conjunction with QD FRET are quite varied and include (i) cleavage-based assays (e. g., proteases, kinases, and DNAzymes) (Figure 6.27) [321,365,368,[526][527][528][529][556][557][558], (ii) conformational change-based assays (e.g., aptamers, binding proteins, and DNA molecular beacons) [518,[559][560][561], (iii) displacement assays (e.g., antibodies and binding proteins) (Figure 6.28) [554,562], (iv) various immunoassays (including direct, displacement, and sandwich) [367,[562][563][564], (v) nucleic acid hybridization [518,555], and (vi) assays based on acceptor spectral changes (mainly pH or ion sensitive dyes) (Figure 6.16) [79, 527,556]. Given the unique photophysical properties of QDs, our increasing fundamental understanding of these unique materials when used in energy transfer configurations, and the availability of improved synthesis and bioconjugation methods, we can expect continued utilization in many FRETbased biological assays, with increasing emphasis on multiplexed and in vivo detection [321,…”
Section: Semiconductor Nanocrystalsmentioning
confidence: 99%
“…There are hosts of biomolecular interactions/processes that are studied using QD energy transfer formats and these include nucleic acid interactions, binding protein conformation changes, antibody binding, aptamer interactions, and protease cleavage [283,513,[515][516][517][518]524,554]. Assay formats found in conjunction with QD FRET are quite varied and include (i) cleavage-based assays (e. g., proteases, kinases, and DNAzymes) (Figure 6.27) [321,365,368,[526][527][528][529][556][557][558], (ii) conformational change-based assays (e.g., aptamers, binding proteins, and DNA molecular beacons) [518,[559][560][561], (iii) displacement assays (e.g., antibodies and binding proteins) (Figure 6.28) [554,562], (iv) various immunoassays (including direct, displacement, and sandwich) [367,[562][563][564], (v) nucleic acid hybridization [518,555], and (vi) assays based on acceptor spectral changes (mainly pH or ion sensitive dyes) (Figure 6.16) [79, 527,556]. Given the unique photophysical properties of QDs, our increasing fundamental understanding of these unique materials when used in energy transfer configurations, and the availability of improved synthesis and bioconjugation methods, we can expect continued utilization in many FRETbased biological assays, with increasing emphasis on multiplexed and in vivo detection [321,…”
Section: Semiconductor Nanocrystalsmentioning
confidence: 99%
“…This can occur over distances of 10-100 Å with the most efficient transfer occurring at 20-60 Å . Therefore; FRET has extensive used in the study of macromolecular interactions, such as protein-protein association, antibody-antigen binding and DNA hybridization (Jamiesona et al 2007;Mattoussi et al 2004;Smith et al 2008;Stringer et al 2008;Xu et al 2006). In this study, FRET was used to provide evidence supporting the accurate antibody orientation on the QD surface.…”
Section: Fluorescence Resonance Energy Transfer Techniquementioning
confidence: 99%
“…Generally for the diagnosis of the disease, Ab based biosensors are preferred (Conroy et al, 2009). Mostly, the sensors are designed to diagnose the disease of veterinary importance as well as having zoonotic importance and vice versa (Stringer et al, 2008;Tran et al, 2012). Some have developed the sensors for surrogate human viruses so as to avoid the direct contact with the human viruses (Connelly et al, 2012).…”
Section: Introductionmentioning
confidence: 99%