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Construction of self-signal DNA electrochemical biosensor employing WS(2) nanosheets combined with PIn6COOH

In this work, a novel self-signal DNA electrochemical biosensor was constructed based on tungsten disulfide (WS(2)) nanosheets combined with poly(indole-6-carboxylic acid) (PIn6COOH) as the sensing interface. The WS(2) nanosheets were synthesized via a simple solvent exfoliation method from bulk WS(...

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Detalles Bibliográficos
Autores principales: Yang, Jimin, Gao, Lei, Peng, Cheng, Zhang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062153/
https://www.ncbi.nlm.nih.gov/pubmed/35520724
http://dx.doi.org/10.1039/c8ra10266j
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author Yang, Jimin
Gao, Lei
Peng, Cheng
Zhang, Wei
author_facet Yang, Jimin
Gao, Lei
Peng, Cheng
Zhang, Wei
author_sort Yang, Jimin
collection PubMed
description In this work, a novel self-signal DNA electrochemical biosensor was constructed based on tungsten disulfide (WS(2)) nanosheets combined with poly(indole-6-carboxylic acid) (PIn6COOH) as the sensing interface. The WS(2) nanosheets were synthesized via a simple solvent exfoliation method from bulk WS(2), and then PIn6COOH was electropolymerized on the WS(2) nanosheet-modified carbon paste electrode to obtain a unique nanocomposite. The electropolymerization efficiency was remarkably improved, ascribed to the physical adsorption between WS(2) nanosheets and aromatic In6COOH monomers, resulting in an increase of the electrochemical response of PIn6COOH. Owing to the presence of π–π interactions between the conjugated PIn6COOH/WS(2) nanocomposite and DNA bases, the probe ssDNA was noncovalently assembled on the nanocomposite substrate. After the hybridization of the probe ssDNA with the target DNA, the formation of the double-helix structure induced the resulting dsDNA to be released from the surface of the conjugated nanocomposite, accompanied with the self-signal regeneration of the nanocomposite (“signal-on”). The constructed PIn6COOH/WS(2) nanocomposite was not only employed as an interface for DNA immobilization but also reflected the signal transduction stemming from DNA immobilization and hybridization without any external indicators or complex labeling processes. A detection limit of 2.3 × 10(−18) mol L(−1) has been estimated and a dynamic range of 1.0 × 10(−17) mol L(−1) to 1.0 × 10(−11) mol L(−1) has been shown for the detection of a PIK3CA gene related to lung cancer. Selectivity of the biosensor has been researched in the presence of noncomplementary and base mismatched DNA sequences.
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spelling pubmed-90621532022-05-04 Construction of self-signal DNA electrochemical biosensor employing WS(2) nanosheets combined with PIn6COOH Yang, Jimin Gao, Lei Peng, Cheng Zhang, Wei RSC Adv Chemistry In this work, a novel self-signal DNA electrochemical biosensor was constructed based on tungsten disulfide (WS(2)) nanosheets combined with poly(indole-6-carboxylic acid) (PIn6COOH) as the sensing interface. The WS(2) nanosheets were synthesized via a simple solvent exfoliation method from bulk WS(2), and then PIn6COOH was electropolymerized on the WS(2) nanosheet-modified carbon paste electrode to obtain a unique nanocomposite. The electropolymerization efficiency was remarkably improved, ascribed to the physical adsorption between WS(2) nanosheets and aromatic In6COOH monomers, resulting in an increase of the electrochemical response of PIn6COOH. Owing to the presence of π–π interactions between the conjugated PIn6COOH/WS(2) nanocomposite and DNA bases, the probe ssDNA was noncovalently assembled on the nanocomposite substrate. After the hybridization of the probe ssDNA with the target DNA, the formation of the double-helix structure induced the resulting dsDNA to be released from the surface of the conjugated nanocomposite, accompanied with the self-signal regeneration of the nanocomposite (“signal-on”). The constructed PIn6COOH/WS(2) nanocomposite was not only employed as an interface for DNA immobilization but also reflected the signal transduction stemming from DNA immobilization and hybridization without any external indicators or complex labeling processes. A detection limit of 2.3 × 10(−18) mol L(−1) has been estimated and a dynamic range of 1.0 × 10(−17) mol L(−1) to 1.0 × 10(−11) mol L(−1) has been shown for the detection of a PIK3CA gene related to lung cancer. Selectivity of the biosensor has been researched in the presence of noncomplementary and base mismatched DNA sequences. The Royal Society of Chemistry 2019-03-26 /pmc/articles/PMC9062153/ /pubmed/35520724 http://dx.doi.org/10.1039/c8ra10266j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Yang, Jimin
Gao, Lei
Peng, Cheng
Zhang, Wei
Construction of self-signal DNA electrochemical biosensor employing WS(2) nanosheets combined with PIn6COOH
title Construction of self-signal DNA electrochemical biosensor employing WS(2) nanosheets combined with PIn6COOH
title_full Construction of self-signal DNA electrochemical biosensor employing WS(2) nanosheets combined with PIn6COOH
title_fullStr Construction of self-signal DNA electrochemical biosensor employing WS(2) nanosheets combined with PIn6COOH
title_full_unstemmed Construction of self-signal DNA electrochemical biosensor employing WS(2) nanosheets combined with PIn6COOH
title_short Construction of self-signal DNA electrochemical biosensor employing WS(2) nanosheets combined with PIn6COOH
title_sort construction of self-signal dna electrochemical biosensor employing ws(2) nanosheets combined with pin6cooh
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062153/
https://www.ncbi.nlm.nih.gov/pubmed/35520724
http://dx.doi.org/10.1039/c8ra10266j
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