Quantum dots nanoparticle-based lateral flow assay for rapid detection of Mycobacterium species using anti-FprA antibodies.
Articolo
Data di Pubblicazione:
2012
Citazione:
Quantum dots nanoparticle-based lateral flow assay for rapid detection of Mycobacterium species using anti-FprA antibodies / Cimaglia, F; Aliverti, A; Chiesa, M; Poltronieri, P; De Lorenzis, E; Santino, A; Sechi, Leonardo Antonio. - In: NANOTECHNOLOGY DEVELOPMENT. - ISSN 2038-968X. - 2:1(2012). [https://doi.org/10.4081/nd.2012.e5]
Abstract:
A lateral flow (LF) device combined with
quantum dots (QDs) technology was developed
for rapid detection of a specific mycobacterial
flavoprotein reductase (fprA). In order to
develop the LF assay based on a double-antibody
sandwich format, two monoclonal antibodies
recognizing different epitopes located
in separated fprA domains were identified. The
first monoclonal antibody was immobilized
onto the detection zone of a porous nitrocellulose
membrane, whereas another monoclonal
antibody was conjugated to QDs nanoparticles
as a detection system. Using these monoclonal
antibodies we recorded a good fluorescence
signal, the intensity of which was directly proportional
to the concentration of fprA protein.
The use of antibodies conjugated with fluorescent
semiconductor QDs via biotin-streptavidin
bridge, allowed the detection of fprA protein
at concentrations as low as 12.5 pg/μL in
less than 10 min. The reported technology
could be useful in the diagnostic investigation
of Mycobacterium tuberculosis and other
human pathogens in clinical specimens
quantum dots (QDs) technology was developed
for rapid detection of a specific mycobacterial
flavoprotein reductase (fprA). In order to
develop the LF assay based on a double-antibody
sandwich format, two monoclonal antibodies
recognizing different epitopes located
in separated fprA domains were identified. The
first monoclonal antibody was immobilized
onto the detection zone of a porous nitrocellulose
membrane, whereas another monoclonal
antibody was conjugated to QDs nanoparticles
as a detection system. Using these monoclonal
antibodies we recorded a good fluorescence
signal, the intensity of which was directly proportional
to the concentration of fprA protein.
The use of antibodies conjugated with fluorescent
semiconductor QDs via biotin-streptavidin
bridge, allowed the detection of fprA protein
at concentrations as low as 12.5 pg/μL in
less than 10 min. The reported technology
could be useful in the diagnostic investigation
of Mycobacterium tuberculosis and other
human pathogens in clinical specimens
Tipologia CRIS:
1.1 Articolo in rivista
Elenco autori:
Cimaglia, F; Aliverti, A; Chiesa, M; Poltronieri, P; De Lorenzis, E; Santino, A; Sechi, Leonardo Antonio
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