Coupled with the ability of fast and quantitative response, electrochemical aptasensors （EA） have great potential in the application of early diagnosis of cancer biomarker. In order to determine the rare hiomarkers ...Coupled with the ability of fast and quantitative response, electrochemical aptasensors （EA） have great potential in the application of early diagnosis of cancer biomarker. In order to determine the rare hiomarkers in the compli- cate clinical samples, scientists are making unremitting efforts towards improving the sensitivity and selectivity of EA. Herein, a ＂sandwich＂-strucmre electrochemical aptasensor （SEA） is developed for analysis of cancer biomarker carcino-embryonic antigen （CEA）. Two DNA aptamers are employed, one of which is thiolated at Y-terminal and immobilized onto the gold electrode as a capture probe, while the other one is served as signal probe. The two ap- tamers could ＂sandwich＂ the target and signal probe is then subjected to the terminal deoxynucleotidyl transferase （TdT）-catalyzed incorporation of biotin labeled dNTPs into its 3＇-terminal. Thus the as-generated long DNA oligo tails allow specific binding of numerous avidin modified horseradish peroxidase （Av-HRP）, resulting in enhanced peroxidase catalyzed electrochemical signals. This signal amplification strategy is termed as surface initiated enzy- matic polymerization （SIEP）. This SIEP amplified SEA has a detection limit of 10 pg·mL^-1, indicating the out- standing amplification efficiency.展开更多
文摘Coupled with the ability of fast and quantitative response, electrochemical aptasensors （EA） have great potential in the application of early diagnosis of cancer biomarker. In order to determine the rare hiomarkers in the compli- cate clinical samples, scientists are making unremitting efforts towards improving the sensitivity and selectivity of EA. Herein, a ＂sandwich＂-strucmre electrochemical aptasensor （SEA） is developed for analysis of cancer biomarker carcino-embryonic antigen （CEA）. Two DNA aptamers are employed, one of which is thiolated at Y-terminal and immobilized onto the gold electrode as a capture probe, while the other one is served as signal probe. The two ap- tamers could ＂sandwich＂ the target and signal probe is then subjected to the terminal deoxynucleotidyl transferase （TdT）-catalyzed incorporation of biotin labeled dNTPs into its 3＇-terminal. Thus the as-generated long DNA oligo tails allow specific binding of numerous avidin modified horseradish peroxidase （Av-HRP）, resulting in enhanced peroxidase catalyzed electrochemical signals. This signal amplification strategy is termed as surface initiated enzy- matic polymerization （SIEP）. This SIEP amplified SEA has a detection limit of 10 pg·mL^-1, indicating the out- standing amplification efficiency.
