Target-modulated competitive binding and exonuclease I-powered strategy for the simultaneous and rapid detection of biological targets
Wang, Yingwen1,2,3; Zhang, Dun1,2,3; Zeng, Yan1,3; Qi, Peng1,2,3
2022-02-15
发表期刊BIOSENSORS & BIOELECTRONICS
ISSN0956-5663
卷号198页码:8
通讯作者Zhang, Dun([email protected]) ; Qi, Peng([email protected])
摘要Simultaneous multiple-target detection is essential for the prevention, identification, and treatment of numerous diseases. In this study, a novel strategy based on target-modulated competitive binding and exonuclease I (Exo I) powered signal molecule release was established with the advantages of rapid response and high selectivity and sensitivity. The strategy holds substantial potential for the development of versatile platforms for the simultaneous detection of biological targets. To mitigate the low load capacity and time-consuming responsive process of the Zr-MOF system, UiO-67 was chosen to replace UiO-66 (a typical Zr-MOF) as the nanocarrier for encapsulating more signal molecules, whereby the assembled double-stranded DNA (dsDNA) structures of UiO-67 acted as gatekeepers to form dsDNA-functionalized MOFs. Additionally, Exo I was introduced into the system to accelerate the release of the signal molecules. In the presence of biological targets, the competitive binding between the targets and aptamers caused the hydrolysis of the free DNA sequence by Exo I, promoting the release of signal molecules and leading to a rapid and significant increase in the fluorescence intensity. For adenosine triphosphate (ATP) and cytochrome c (cyt c), which were chosen as model biological targets, this sensor displayed detection limits as low as 5.03 and 6.11 fM, respectively. Moreover, the developed biosensor was successfully applied to the simultaneous detection of ATP and cyt c in spiked serum samples. Therefore, this strategy provides guidance for further research of biosensors for simultaneous multiple-target detection and propels the application of MOF carriers in biomedicine.
关键词Simultaneous multiple-target detection UiO-67 Exonuclease I-Powered signal molecule release ATP cyt c
DOI10.1016/j.bios.2021.113817
收录类别SCI
语种英语
资助项目National Natural Science Foundation of China[41876101]; National Natural Science Foundation of China[41906037]; Nantong Scientific Plan Foundation[JC2021054]; Nantong Scientific Plan Foundation[2020NT04]
WOS研究方向Biophysics ; Biotechnology & Applied Microbiology ; Chemistry ; Electrochemistry ; Science & Technology - Other Topics
WOS类目Biophysics ; Biotechnology & Applied Microbiology ; Chemistry, Analytical ; Electrochemistry ; Nanoscience & Nanotechnology
WOS记录号WOS:000781104400008
出版者ELSEVIER ADVANCED TECHNOLOGY
引用统计
被引频次:13[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.qdio.ac.cn/handle/337002/178820
专题海洋环境腐蚀与生物污损重点实验室
通讯作者Zhang, Dun; Qi, Peng
作者单位1.Chinese Acad Sci, Inst Oceanol, Key Lab Marine Environm Corros & Biofouling, Qingdao 266071, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100039, Peoples R China
3.Pilot Natl Lab Marine Sci & Technol Qingdao, Open Studio Marine Corros & Protect, 1 Wenhai Rd, Qingdao 266237, Peoples R China
第一作者单位中国科学院海洋研究所
通讯作者单位中国科学院海洋研究所
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GB/T 7714
Wang, Yingwen,Zhang, Dun,Zeng, Yan,et al. Target-modulated competitive binding and exonuclease I-powered strategy for the simultaneous and rapid detection of biological targets[J]. BIOSENSORS & BIOELECTRONICS,2022,198:8.
APA Wang, Yingwen,Zhang, Dun,Zeng, Yan,&Qi, Peng.(2022).Target-modulated competitive binding and exonuclease I-powered strategy for the simultaneous and rapid detection of biological targets.BIOSENSORS & BIOELECTRONICS,198,8.
MLA Wang, Yingwen,et al."Target-modulated competitive binding and exonuclease I-powered strategy for the simultaneous and rapid detection of biological targets".BIOSENSORS & BIOELECTRONICS 198(2022):8.
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