On-demand controlled bidirectional DNAzyme path for ultra-sensitive heavy metal ion detection
文献类型:期刊论文
作者 | Xu, Jing1; Li, Yujin1,2; Wang, Futing2; Luo, Xinqi1; Zhang, Wei6; Lyu, Yifan2; Yang, Hongfen5; Cai, Ren2; Tan, Weihong2,3,4 |
刊名 | CHEMICAL SCIENCE
![]() |
出版日期 | 2024-10-11 |
ISSN号 | 2041-6520 |
DOI | 10.1039/d4sc04404e |
通讯作者 | Cai, Ren(cairen@hnu.edu.cn) |
英文摘要 | A bidirectional self-powered biosensor is constructed for the quasi-simultaneous detection of Pb2+ and Hg2+ based on MoS2@CuS heterostructures as an accelerator and hybridization chain reaction (HCR) as a signal amplification strategy. MoS2@CuS heterostructures significantly facilitate electron transfer between glucose and bioelectrodes, thereby greatly improving the detection signal of self-powered biosensors. This novel biosensor employs the unique sequences of DNAzymes to isolate Pb2+ and Hg2+ by the cleavage effect and thymine (T)-Hg2+-thymine (T) structures, respectively. In the process, Pb2+ cuts the sequence of DNAzyme at the bioanode to trigger glucose oxidation to monitor Pb2+. The as-formed T-Hg2+-T structures activate HCR to reduce [Ru(NH3)6]3+ to detect Hg2+ at the biocathode. It is noteworthy that this biosensor not only realizes Pb2+ or Hg2+ detection in a single-electrode, respectively, but also can quasi-simultaneously detect both Pb2+ and Hg2+ in the bioanode and the biocathode. The novel self-powered biosensor identifies Pb2+ in the range of 106 fM to 10 fM with a limit of detection (LOD) of 3.1 fM and Hg2+ in the range of 106 fM to 1 fM with an LOD of 0.33 fM. A bidirectional self-powered biosensor is constructed for the quasi-simultaneous detection of Pb2+ and Hg2+ based on MoS2@CuS heterostructures as an accelerator and hybridization chain reaction as a signal amplification strategy. |
WOS关键词 | SENSOR |
资助项目 | Natural Science Foundation of Hunan Province[235200810056] ; Joint Fund Project for Technology Research and Development Plan of Henan Technology[2024JJ5348] ; Joint Fund Project for Technology Research and Development Plan of Henan Technology[2021JJ20020] ; Hunan Provincial Natural Science Foundation of China[22004032] ; National Natural Science Foundation of China ; Dabie Mountain Laboratory, Nanhu Scholars Program for Young Scholars of XYNU |
WOS研究方向 | Chemistry |
语种 | 英语 |
WOS记录号 | WOS:001331184200001 |
出版者 | ROYAL SOC CHEMISTRY |
资助机构 | Natural Science Foundation of Hunan Province ; Joint Fund Project for Technology Research and Development Plan of Henan Technology ; Hunan Provincial Natural Science Foundation of China ; National Natural Science Foundation of China ; Dabie Mountain Laboratory, Nanhu Scholars Program for Young Scholars of XYNU |
源URL | [http://ir.hfcas.ac.cn:8080/handle/334002/134579] ![]() |
专题 | 中国科学院合肥物质科学研究院 |
通讯作者 | Cai, Ren |
作者单位 | 1.Xinyang Normal Univ, Coll Chem & Chem Engn, Xinyang 464000, Peoples R China 2.Hunan Univ, Coll Mat Sci & Engn, Coll Chem & Chem Engn, Mol Sci & Biomed Lab,State Key Lab Chemobio Sensin, Changsha 410082, Hunan, Peoples R China 3.Chinese Acad Sci, Univ Chinese Acad Sci, Zhejiang Canc Hosp, Hangzhou Inst Med,Canc Hosp, Hangzhou 310022, Zhejiang, Peoples R China 4.Shanghai Jiao Tong Univ, Renji Hosp, Inst Mol Med, Coll Chem & Chem Engn,Sch Med, Shanghai 200240, Peoples R China 5.Univ South China, Sch Publ Hlth, Hengyang Med Sch, Hunan Key Lab Typ Environm Pollut & Hlth Hazards, Hengyang 421001, Peoples R China 6.Xinyang Normal Univ, Coll Life Sci, Dabie Mt Lab, Xinyang 464000, Peoples R China |
推荐引用方式 GB/T 7714 | Xu, Jing,Li, Yujin,Wang, Futing,et al. On-demand controlled bidirectional DNAzyme path for ultra-sensitive heavy metal ion detection[J]. CHEMICAL SCIENCE,2024. |
APA | Xu, Jing.,Li, Yujin.,Wang, Futing.,Luo, Xinqi.,Zhang, Wei.,...&Tan, Weihong.(2024).On-demand controlled bidirectional DNAzyme path for ultra-sensitive heavy metal ion detection.CHEMICAL SCIENCE. |
MLA | Xu, Jing,et al."On-demand controlled bidirectional DNAzyme path for ultra-sensitive heavy metal ion detection".CHEMICAL SCIENCE (2024). |
入库方式: OAI收割
来源:合肥物质科学研究院
浏览0
下载0
收藏0
其他版本
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。