TY - JOUR
T1 - Organophosphonate-based PNA-functionalization of silicon nanowires for label-free DNA detection
AU - Cattani-Scholz, Anna
AU - Pedone, Daniel
AU - Dubey, Manish
AU - Neppl, Stefan
AU - Nickel, Bert
AU - Feulner, Peter
AU - Schwartz, Jeffrey
AU - Absteiter, Gerhard
AU - Tornow, Marc
PY - 2008/8
Y1 - 2008/8
N2 - We investigated hydroxyalkylphosphonate monolayers as a novel platform for the biofunctionalization of silicon-based field effect sensor devices. This included a detailed study of the thin film properties of organophosphonate films on Si substrates using several surface analysis techniques, including AFM, ellipsometry, contact angle, X-ray photoelectron spectroscopy (XPS), X-ray reflectivity, and current-voltage characteristics in electrolyte solution. Our results indicate the formation of a dense monolayer on the native silicon oxide that has excellent passivation properties. The monolayer was biofunctionalized with 12 mer pepticle nucleic acid (PNA) receptor molecules in a two-step procedure using the heterobifunctional linker, 3-maleimidopropionic-acid- N-hydroxysuccinimidester. Successful surface modification with the probe PNA was verified by XPS and contact angle measurements, and hybridization with DNA was determined by fluorescence measurements. Finally, the PNA functionalization protocol was translated to 2 μm long, 100 nm wide Si nanowire field effect devices, which were successfully used for label-free DNA/PNA hybridization detection.
AB - We investigated hydroxyalkylphosphonate monolayers as a novel platform for the biofunctionalization of silicon-based field effect sensor devices. This included a detailed study of the thin film properties of organophosphonate films on Si substrates using several surface analysis techniques, including AFM, ellipsometry, contact angle, X-ray photoelectron spectroscopy (XPS), X-ray reflectivity, and current-voltage characteristics in electrolyte solution. Our results indicate the formation of a dense monolayer on the native silicon oxide that has excellent passivation properties. The monolayer was biofunctionalized with 12 mer pepticle nucleic acid (PNA) receptor molecules in a two-step procedure using the heterobifunctional linker, 3-maleimidopropionic-acid- N-hydroxysuccinimidester. Successful surface modification with the probe PNA was verified by XPS and contact angle measurements, and hybridization with DNA was determined by fluorescence measurements. Finally, the PNA functionalization protocol was translated to 2 μm long, 100 nm wide Si nanowire field effect devices, which were successfully used for label-free DNA/PNA hybridization detection.
KW - Biosensor
KW - DNA/PNA hybridization
KW - Heterobifunctional linker
KW - Organophosphonate monolayers
KW - Silicon nanowire device
KW - Surface characterization
KW - X-ray reflectivity
KW - XPS
UR - http://www.scopus.com/inward/record.url?scp=51849122512&partnerID=8YFLogxK
U2 - 10.1021/nn800136e
DO - 10.1021/nn800136e
M3 - Article
C2 - 19206369
AN - SCOPUS:51849122512
SN - 1936-0851
VL - 2
SP - 1653
EP - 1660
JO - ACS Nano
JF - ACS Nano
IS - 8
ER -