{"title":"A Fluorescent Aptamer Sensor for Detecting Golgi Protein 73 Based on Magnetic Ferroferric Oxide@Boron, Nitrogen-Doped Graphene Quantum Dots.","authors":"Guiyin Li, Wei He, Ruijie Yan, Xuanlong Su, Tingting Yu, Xiaohong Tan, Yong Huang","doi":"10.1002/bab.70006","DOIUrl":null,"url":null,"abstract":"<p><p>In this paper, a fluorescent aptamer sensor based on magnetic ferroferric oxide@boron, nitrogen-doped graphene quantum dots (Fe<sub>3</sub>O<sub>4</sub>@B,N-GQDs) was developed to detect Golgi protein 73 (GP73). GP73 aptamer (GP73<sub>Apt</sub>) functioned with Fe<sub>3</sub>O<sub>4</sub>@B,N-GQDs (Fe<sub>3</sub>O<sub>4</sub>@B,N-GQDs-GP73<sub>Apt</sub>) and was used as the fluorescent donor, while molybdenum disulfide (MoS<sub>2</sub>) with a large surface served as the fluorescent acceptor. The fluorescence of Fe<sub>3</sub>O<sub>4</sub>@B,N-GQDs-GP73<sub>Apt</sub> was quenched by MoS<sub>2</sub> based on the fluorescence resonance energy transfer (FRET) principle. However, in the presence of GP73, Fe<sub>3</sub>O<sub>4</sub>@B,N-GQDs-GP73<sub>Apt</sub> could specifically bind to GP73, forming a Fe<sub>3</sub>O<sub>4</sub>@B,N-GQDs-GP73<sub>Apt</sub>-GP73 complex. This binding event caused Fe<sub>3</sub>O<sub>4</sub>@B,N-GQDs-GP73<sub>Apt</sub> to move away from the surface of MoS<sub>2</sub>, thus blocking the FRET process and recovering the fluorescence. Under optimal conditions, a linear relationship was established between the fluorescence recovery and the concentration of GP73 within the range of 10-1000 ng/mL (R<sup>2 </sup>= 0.9918), and the limit of detection was 7.37 ng/mL. Additionally, when the sensor was applied to test actual samples, the recovery rates were in the range of 98.80%-101.18%, and the relative standard deviations were between 0.29%-3.04%. These findings demonstrated the excellent detection performance of the proposed fluorescent aptamer sensor.</p>","PeriodicalId":9274,"journal":{"name":"Biotechnology and applied biochemistry","volume":" ","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biotechnology and applied biochemistry","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1002/bab.70006","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
In this paper, a fluorescent aptamer sensor based on magnetic ferroferric oxide@boron, nitrogen-doped graphene quantum dots (Fe3O4@B,N-GQDs) was developed to detect Golgi protein 73 (GP73). GP73 aptamer (GP73Apt) functioned with Fe3O4@B,N-GQDs (Fe3O4@B,N-GQDs-GP73Apt) and was used as the fluorescent donor, while molybdenum disulfide (MoS2) with a large surface served as the fluorescent acceptor. The fluorescence of Fe3O4@B,N-GQDs-GP73Apt was quenched by MoS2 based on the fluorescence resonance energy transfer (FRET) principle. However, in the presence of GP73, Fe3O4@B,N-GQDs-GP73Apt could specifically bind to GP73, forming a Fe3O4@B,N-GQDs-GP73Apt-GP73 complex. This binding event caused Fe3O4@B,N-GQDs-GP73Apt to move away from the surface of MoS2, thus blocking the FRET process and recovering the fluorescence. Under optimal conditions, a linear relationship was established between the fluorescence recovery and the concentration of GP73 within the range of 10-1000 ng/mL (R2 = 0.9918), and the limit of detection was 7.37 ng/mL. Additionally, when the sensor was applied to test actual samples, the recovery rates were in the range of 98.80%-101.18%, and the relative standard deviations were between 0.29%-3.04%. These findings demonstrated the excellent detection performance of the proposed fluorescent aptamer sensor.
期刊介绍:
Published since 1979, Biotechnology and Applied Biochemistry is dedicated to the rapid publication of high quality, significant research at the interface between life sciences and their technological exploitation.
The Editors will consider papers for publication based on their novelty and impact as well as their contribution to the advancement of medical biotechnology and industrial biotechnology, covering cutting-edge research in synthetic biology, systems biology, metabolic engineering, bioengineering, biomaterials, biosensing, and nano-biotechnology.