Liang Zhou , Tiantian Li , Shuaibing Yu , Pengnan Yao , Jinming Kong , Xueji Zhang
{"title":"Detection of potential biomarkers for esophageal cancer based on fluorescent biosensor","authors":"Liang Zhou , Tiantian Li , Shuaibing Yu , Pengnan Yao , Jinming Kong , Xueji Zhang","doi":"10.1016/j.bej.2025.109860","DOIUrl":null,"url":null,"abstract":"<div><div>Fluorescent biosensors have garnered significant interest due to their high sensitivity, efficiency, and rapid detection capabilities, making them an attractive alternative for various diagnostic applications. To address these needs, we developed a fluorescence-based biosensor using magnetic beads for the rapid and precise detection of miRNA-320b, a potential biomarker for esophageal cancer. The process begins by immobilizing DNA onto the surface of magnetic beads. Upon the introduction of miRNA-320b, a stable DNA-RNA duplex forms through complementary base pairing. In this biosensor design, 3-aminophenylboric acid serves as a \"crosslinker\" to connect carboxyfluorescein to miRNA-320b. The design relies on the cis-diol structure at the 3′ end of miRNA-320b, which forms a covalent bond with phenylboric acid via borate esterification, enabling the specific differentiation of miRNA-320b from DNA. The use of magnetic beads facilitates rapid separation and purification, minimizing interference and enhancing the detection of the esophageal cancer biomarker miRNA-320b. Following optimization, the biosensor displayed a linear range from 10⁻¹ ⁴ to 10⁻⁹ M with a minimum detection limit of 1.42 fM. This innovative fluorescent biosensor offers a novel, efficient, and straightforward approach for the early screening of esophageal cancer.</div></div>","PeriodicalId":8766,"journal":{"name":"Biochemical Engineering Journal","volume":"223 ","pages":"Article 109860"},"PeriodicalIF":3.7000,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemical Engineering Journal","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1369703X25002347","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Fluorescent biosensors have garnered significant interest due to their high sensitivity, efficiency, and rapid detection capabilities, making them an attractive alternative for various diagnostic applications. To address these needs, we developed a fluorescence-based biosensor using magnetic beads for the rapid and precise detection of miRNA-320b, a potential biomarker for esophageal cancer. The process begins by immobilizing DNA onto the surface of magnetic beads. Upon the introduction of miRNA-320b, a stable DNA-RNA duplex forms through complementary base pairing. In this biosensor design, 3-aminophenylboric acid serves as a "crosslinker" to connect carboxyfluorescein to miRNA-320b. The design relies on the cis-diol structure at the 3′ end of miRNA-320b, which forms a covalent bond with phenylboric acid via borate esterification, enabling the specific differentiation of miRNA-320b from DNA. The use of magnetic beads facilitates rapid separation and purification, minimizing interference and enhancing the detection of the esophageal cancer biomarker miRNA-320b. Following optimization, the biosensor displayed a linear range from 10⁻¹ ⁴ to 10⁻⁹ M with a minimum detection limit of 1.42 fM. This innovative fluorescent biosensor offers a novel, efficient, and straightforward approach for the early screening of esophageal cancer.
期刊介绍:
The Biochemical Engineering Journal aims to promote progress in the crucial chemical engineering aspects of the development of biological processes associated with everything from raw materials preparation to product recovery relevant to industries as diverse as medical/healthcare, industrial biotechnology, and environmental biotechnology.
The Journal welcomes full length original research papers, short communications, and review papers* in the following research fields:
Biocatalysis (enzyme or microbial) and biotransformations, including immobilized biocatalyst preparation and kinetics
Biosensors and Biodevices including biofabrication and novel fuel cell development
Bioseparations including scale-up and protein refolding/renaturation
Environmental Bioengineering including bioconversion, bioremediation, and microbial fuel cells
Bioreactor Systems including characterization, optimization and scale-up
Bioresources and Biorefinery Engineering including biomass conversion, biofuels, bioenergy, and optimization
Industrial Biotechnology including specialty chemicals, platform chemicals and neutraceuticals
Biomaterials and Tissue Engineering including bioartificial organs, cell encapsulation, and controlled release
Cell Culture Engineering (plant, animal or insect cells) including viral vectors, monoclonal antibodies, recombinant proteins, vaccines, and secondary metabolites
Cell Therapies and Stem Cells including pluripotent, mesenchymal and hematopoietic stem cells; immunotherapies; tissue-specific differentiation; and cryopreservation
Metabolic Engineering, Systems and Synthetic Biology including OMICS, bioinformatics, in silico biology, and metabolic flux analysis
Protein Engineering including enzyme engineering and directed evolution.