Avidin-modified polyaniline (PANI) electrochemically deposited onto a Pt disk electrode has been utilized for direct detection of Escherichia coli by immobilizing a 5'-biotin-labeled E. coli probe (BdE) using a differential pulse voltammetric technique in the presence of methylene blue as a DNA hybridization indicator. Depending on the target sample and the sonication time, this BdE-avidin-PANI bioelectrode can be utilized to electrochemically detect a complementary target probe (0.009 ng/microL), E. coli genomic DNA (0.01 ng/microL) and 11 E. coli cells/mL in 60 s to 14 min (hybridization time) without using PCR and can be used 5-7 times at temperatures of 30-45 degrees C.
Cysteine modified NH 2 -end peptide nucleic acid (PNA) (24-mer) probe and 5¢-thiol end labeled deoxyribonucleic acid (DNA) probes specific to Mycobacterium tuberculosis have been immobilized onto BK-7 gold coated glass plates for the detection of complementary, one-base mismatch, non-complementary targets and complementary target sequence in genomic DNA of Mycobacterium tuberculosis using a surface plasmon resonance (SPR) technique. The DNA/Au and PNA/Au bio-electrodes have been characterized using contact angle, atomic force microscopy (AFM), electrochemical impedance spectroscopy (EIS) and cyclic voltammetric (CV) techniques, respectively. It is revealed that there is a 252 millidegrees SPR angle change in the case of PNA immobilization and 205 millidegrees for DNA immobilization, indicating increased amount of immobilized PNA molecules. Hybridization studies reveal that there is no binding of the non-complementary target to DNA/Au and PNA/Au electrode. Compared to the DNA/Au bioelectrode, PNA/Au electrode has been found to be more efficient for detection of one-base mismatch sequence. The PNA/Au bioelectrode shows better detection limit (1.0 ng ml -1 ) over the DNA-Au bioelectrode (3.0 ng ml -1 ). The values of the association (k a ) and dissociation rate constant (k d ) for the complementary sequence in case of the PNA/Au bioelectrode have been estimated as 8.5 ¥ 10 4 m -1 s -1 and 3.6 ¥ 10 -3 s -1 , respectively.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.