TY - JOUR
T1 - Detection of the carcinogenic water pollutant benzo [a]pyrene with an electro-switchable biosurface
AU - Lux, Gregor
AU - Langer, Andreas
AU - Pschenitza, Michael
AU - Karsunke, Xaver
AU - Strasser, Ralf
AU - Niessner, Reinhard
AU - Knopp, Dietmar
AU - Rant, Ulrich
N1 - Publisher Copyright:
© 2015 American Chemical Society.
PY - 2015/4/21
Y1 - 2015/4/21
N2 - The toxic nature of polycyclic aromatic hydrocarbons (PAHs), in particular benzo[a]pyrene (B[a]P), neccessitates the monitoring of PAH contamination levels in food and the environment. Here we introduce an indirect immunoassay format using electro-switchable biosurfaces (ESB) for the detection of B[a]P in water. The association of anti-B[a]P antibodies to microelectrodes is analyzed in real-time by measuring changes in the oscillation dynamics of DNA nanolever probes, which are driven to switch their orientations by high-frequency electrical actuation. From the association kinetics, the active concentration of anti-B[a]P, and hence the B[a]P contamination of the sample, can be determined with picomolar sensitivity. The detection limit of the assay improves with measurement time because increasingly accurate analyses of the binding kinetics become possible. It is demonstrated that an exceedance of the permissible 10 ng/L (40 pM) limit for B[a]P is detectable in an unprecedented short assay time (<1 h), using a simple three-step workflow involving minimal sample preparation. The reproducibility was satisfying with standard deviations below 5%. Further, the utility of the assay for practical applications is exemplified by analyzing a river water sample.
AB - The toxic nature of polycyclic aromatic hydrocarbons (PAHs), in particular benzo[a]pyrene (B[a]P), neccessitates the monitoring of PAH contamination levels in food and the environment. Here we introduce an indirect immunoassay format using electro-switchable biosurfaces (ESB) for the detection of B[a]P in water. The association of anti-B[a]P antibodies to microelectrodes is analyzed in real-time by measuring changes in the oscillation dynamics of DNA nanolever probes, which are driven to switch their orientations by high-frequency electrical actuation. From the association kinetics, the active concentration of anti-B[a]P, and hence the B[a]P contamination of the sample, can be determined with picomolar sensitivity. The detection limit of the assay improves with measurement time because increasingly accurate analyses of the binding kinetics become possible. It is demonstrated that an exceedance of the permissible 10 ng/L (40 pM) limit for B[a]P is detectable in an unprecedented short assay time (<1 h), using a simple three-step workflow involving minimal sample preparation. The reproducibility was satisfying with standard deviations below 5%. Further, the utility of the assay for practical applications is exemplified by analyzing a river water sample.
UR - http://www.scopus.com/inward/record.url?scp=84928324561&partnerID=8YFLogxK
U2 - 10.1021/acs.analchem.5b00648
DO - 10.1021/acs.analchem.5b00648
M3 - Article
C2 - 25822755
AN - SCOPUS:84928324561
SN - 0003-2700
VL - 87
SP - 4538
EP - 4545
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 8
ER -