Your browser doesn't support javascript.
loading
Cascaded signal amplification via target-triggered formation of aptazyme for sensitive electrochemical detection of ATP.
Li, Xia; Yang, Jianmei; Xie, Jiaqing; Jiang, Bingying; Yuan, Ruo; Xiang, Yun.
Affiliation
  • Li X; Key Laboratory of Luminescent and Real-Time Analytical Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.
  • Yang J; Key Laboratory of Luminescent and Real-Time Analytical Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.
  • Xie J; School of Chemistry and Chemical Engineering, Chongqing University of Technology, Chongqing 400054, PR China.
  • Jiang B; School of Chemistry and Chemical Engineering, Chongqing University of Technology, Chongqing 400054, PR China. Electronic address: jiangby@cqut.edu.cn.
  • Yuan R; Key Laboratory of Luminescent and Real-Time Analytical Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.
  • Xiang Y; Key Laboratory of Luminescent and Real-Time Analytical Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China. Electronic address: yunatswu@swu.edu.cn.
Biosens Bioelectron ; 102: 296-300, 2018 Apr 15.
Article in En | MEDLINE | ID: mdl-29156404
The construction of reliable sensors for adenosine triphosphate (ATP) detection gains increasing interest because of its important roles in various enzymatic activities and biological processes. Based on a cascaded, significant signal amplification approach by the integration of the aptazymes and catalytic hairpin assembly (CHA), we have developed a sensitive electrochemical sensor for the detection of ATP. The target ATP leads to the conformational change of the aptazyme sequences and their association with the hairpin substrates to form active aptazymes, in which the hairpin substrates are cyclically cleaved by the metal ion cofactors in buffer to release the enzymatic sequences that can also bind the hairpin substrates to generate active DNAzymes. The catalytic cleavage of the hairpin substrates in the aptazymes/DNAzymes thus results in the generation of a large number of intermediate sequences. Subsequently, these intermediate sequences trigger catalytic capture of many methylene blue-tagged signal sequences on the electrode surface through CHA, producing significantly amplified current response for sensitive detection of ATP at 0.6nM. Besides, the developed sensor can discriminate ATP from analogous interference molecules and be applied to human serum samples, making the sensor a useful addition to the arena for sensitive detection of small molecules.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biosensing Techniques / Adenosine Triphosphate / DNA, Catalytic / Electrochemical Techniques Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Biosens Bioelectron Journal subject: BIOTECNOLOGIA Year: 2018 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biosensing Techniques / Adenosine Triphosphate / DNA, Catalytic / Electrochemical Techniques Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Biosens Bioelectron Journal subject: BIOTECNOLOGIA Year: 2018 Document type: Article Country of publication: United kingdom