We have demonstrated the preliminary results of the in situ monitoring capability of an inhibitor resistant gene quantification assay using magnetic bead (MB) and quantum dot (QD) nanoparticles (hereafter "MB-QD assay") for the detection of E. coli O157:H7 in environmental samples. The selectivity of the MB-QD assay was demonstrated via the discrimination of the target bacteria in the presence of nonspecific microbial populations. The effect of temperature on the assay was examined to evaluate the necessity of elevated temperature incubation. The reagents (i.e., particle complex and particle-DNA conjugate) were also shown to have a stability of at least 10 days without refrigeration, therefore enabling prior preparation and the subsequent storage of these reagents. In addition, it was found that the MB-QD assay was resistant to the presence of naturally occurring inhibitors (i.e., humic acids, Ca(2+)) and residual reagents from DNA extraction (i.e., surfactant, ethanol). Overall the results indicated that the MB-QD assay is potentially suitable for further development as an in situ bacteria monitoring method for working with inhibitor laden samples without requiring additional purification steps and elevated temperature processes.
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http://dx.doi.org/10.1039/c0em00566e | DOI Listing |
Elife
March 2022
Université Paris Cité, CNRS, Institut Jacques Monod, Paris, France.
Centrioles are formed by microtubule triplets in a ninefold symmetric arrangement. In flagellated protists and animal multiciliated cells, accessory structures tethered to specific triplets render the centrioles rotationally asymmetric, a property that is key to cytoskeletal and cellular organization in these contexts. In contrast, centrioles within the centrosome of animal cells display no conspicuous rotational asymmetry.
View Article and Find Full Text PDFACS Appl Mater Interfaces
May 2017
Department of Environmental Science and Engineering, Ewha Womans University, Seoul 03760, Republic of Korea.
For the sensitive quantification of bisphenol A (BPA), we have developed NanoAptamer assay, which employs aptamer and complementary signaling DNA, a set of quantum dots (QD), and magnetic beads (MBs). Signaling DNA-QD was tethered to MB-QD via the aptamer. The affinity of the aptamer to BPA resulted in the release of the signaling DNA-QD from the complex and hence the corresponding decrease in the QD fluorescence measurement signal.
View Article and Find Full Text PDFJ Environ Monit
May 2011
Department of Civil Engineering, Auburn University, Auburn, AL 36849, USA.
We have demonstrated the preliminary results of the in situ monitoring capability of an inhibitor resistant gene quantification assay using magnetic bead (MB) and quantum dot (QD) nanoparticles (hereafter "MB-QD assay") for the detection of E. coli O157:H7 in environmental samples. The selectivity of the MB-QD assay was demonstrated via the discrimination of the target bacteria in the presence of nonspecific microbial populations.
View Article and Find Full Text PDFAnal Chim Acta
September 2010
Department of Civil Engineering, Auburn University, Auburn, AL 36849, USA.
The development and characterization of a magnetic bead (MB)-quantum dot (QD) nanoparticles based assay capable of quantifying pathogenic bacteria is presented here. The MB-QD assay operates by having a capturing probe DNA selectively linked to the signaling probe DNA via the target genomic DNA (gDNA) during DNA hybridization. The signaling probe DNA is labeled with fluorescent QD(565) which serves as a reporter.
View Article and Find Full Text PDFNucleic Acids Res
September 2007
Department of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104, USA.
There have been a growing number of studies where molecular beacons (MBs) are used to image RNA expression in living cells; however, the ability to make accurate measurements can be hampered by the generation of false-positive signals resulting from non-specific interactions and/or nuclease degradation. In the present study, we found that such non-specific signals only arise in the nucleus of living cells. When MBs are retained in the cytoplasmic compartment, by linking them to quantum dots (QDs), false-positive signals are reduced to marginal levels.
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