{"title":"基于分子夹心 DNA 酶催化反应的抗原蛋白高效纳米孔电检测技术","authors":"Lebing Wang, Shou Zhou, Yunjiao Wang, Yan Wang, Jing Li, Xiaohan Chen, Daming Zhou, Liyuan Liang, Bohua Yin, Youwen Zhang, Liang Wang","doi":"10.1039/d4fd00146j","DOIUrl":null,"url":null,"abstract":"Despite significant advances in nanopore nucleic acids sequencing and sensing, proteins detection remains challenging due to the complexity of inherent protein molecular properties (i.e., net charges, polarity, molecular conformation & dimension) and sophisticated environmental parameters (i.e., biofluids), resulting in unsatisfied electrical signal resolution for proteins detection such as poor accessibility, selectivity and sensitivity. The selection of an appropriate electroanalytical approach is strongly desired which should be capable of offering easily detectable and readable signals regarding proteins particularly depending on the practical application. Herein, a molecular sandwich-based DNAzyme catalytic reaction cooperated nanopore detecting approach was designed. Especially, this approach is given the easy use of Mg2+ catalyzed DNAzyme (10-23) toward nucleic acids digestion for efficient antigen protein examination. Its applicability within the proposed strategy operates by initial formation of a molecular sandwich containing capture antibody-antigen-detection antibody for efficiently entrapment of target proteins (herein taking HIV p24 antigen for example) and immobilized on magnetic beads surface. After that, the DNAzyme was linked to the detection antibody via biotin−streptavidin interaction. In the presence of Mg2+, DNAzyme catalytic reaction was triggered to digest nucleic acids substrates and release unique cleavage fragments as reporters capable of transducing easier detectable nucleic acids as substitute of complicated and difficulty-yielded protein signals, in a nanopore. Notably, experimental validation confirms the detecting stability and sensitivity for target antigen referenced with other antigen proteins, meanwhile demonstrates the detection efficacy in human serum environment at very low concentration (LoD ~1.24 pM). This DNAzyme cooperated nanopore electroanalytical approach denotes an advancement in protein examination, may benefit in vitro test of proteinic biomarkers for disease diagnosis and prognosis assessment.","PeriodicalId":76,"journal":{"name":"Faraday Discussions","volume":"95 1","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Molecular sandwich-based DNAzyme catalytic reaction towards transducing efficient nanopore electrical detection for antigen proteins\",\"authors\":\"Lebing Wang, Shou Zhou, Yunjiao Wang, Yan Wang, Jing Li, Xiaohan Chen, Daming Zhou, Liyuan Liang, Bohua Yin, Youwen Zhang, Liang Wang\",\"doi\":\"10.1039/d4fd00146j\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Despite significant advances in nanopore nucleic acids sequencing and sensing, proteins detection remains challenging due to the complexity of inherent protein molecular properties (i.e., net charges, polarity, molecular conformation & dimension) and sophisticated environmental parameters (i.e., biofluids), resulting in unsatisfied electrical signal resolution for proteins detection such as poor accessibility, selectivity and sensitivity. The selection of an appropriate electroanalytical approach is strongly desired which should be capable of offering easily detectable and readable signals regarding proteins particularly depending on the practical application. Herein, a molecular sandwich-based DNAzyme catalytic reaction cooperated nanopore detecting approach was designed. Especially, this approach is given the easy use of Mg2+ catalyzed DNAzyme (10-23) toward nucleic acids digestion for efficient antigen protein examination. Its applicability within the proposed strategy operates by initial formation of a molecular sandwich containing capture antibody-antigen-detection antibody for efficiently entrapment of target proteins (herein taking HIV p24 antigen for example) and immobilized on magnetic beads surface. After that, the DNAzyme was linked to the detection antibody via biotin−streptavidin interaction. In the presence of Mg2+, DNAzyme catalytic reaction was triggered to digest nucleic acids substrates and release unique cleavage fragments as reporters capable of transducing easier detectable nucleic acids as substitute of complicated and difficulty-yielded protein signals, in a nanopore. Notably, experimental validation confirms the detecting stability and sensitivity for target antigen referenced with other antigen proteins, meanwhile demonstrates the detection efficacy in human serum environment at very low concentration (LoD ~1.24 pM). This DNAzyme cooperated nanopore electroanalytical approach denotes an advancement in protein examination, may benefit in vitro test of proteinic biomarkers for disease diagnosis and prognosis assessment.\",\"PeriodicalId\":76,\"journal\":{\"name\":\"Faraday Discussions\",\"volume\":\"95 1\",\"pages\":\"\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2024-08-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Faraday Discussions\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d4fd00146j\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Faraday Discussions","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d4fd00146j","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
尽管在纳米孔核酸测序和传感方面取得了重大进展,但由于蛋白质固有的分子特性(如净电荷、极性、分子构象和ampamp;尺寸)和复杂的环境参数(如生物流体)的复杂性,蛋白质检测仍面临挑战,导致蛋白质检测的电信号分辨率不理想,如可及性、选择性和灵敏度差。因此,选择一种适当的电分析方法是非常必要的,这种方法应能提供易于检测和读取的蛋白质信号,特别是在实际应用中。在此,我们设计了一种基于 DNA 酶催化反应的分子三明治式纳米孔检测方法。特别是,这种方法易于使用 Mg2+ 催化的 DNA 酶(10-23)对核酸进行消化,从而实现高效的抗原蛋白检测。它在拟议策略中的适用性是,首先形成一个分子夹心层,其中包含捕获抗体-抗原-检测抗体,以有效捕获目标蛋白(此处以 HIV p24 抗原为例),并固定在磁珠表面。然后,DNA 酶通过生物素-链霉亲和素相互作用与检测抗体相连。在 Mg2+ 的存在下,DNA 酶的催化反应被触发,消化核酸底物,释放出独特的裂解片段作为报告物,能够在纳米孔中转导更容易检测的核酸,以替代复杂和难以产生的蛋白质信号。值得注意的是,实验验证证实了目标抗原与其他抗原蛋白的检测稳定性和灵敏度,同时证明了在人体血清环境中极低浓度(LoD ~1.24 pM)的检测功效。这种 DNA 酶协同纳米孔电分析方法标志着蛋白质检测技术的进步,可能有利于体外检测蛋白质生物标志物,以进行疾病诊断和预后评估。
Molecular sandwich-based DNAzyme catalytic reaction towards transducing efficient nanopore electrical detection for antigen proteins
Despite significant advances in nanopore nucleic acids sequencing and sensing, proteins detection remains challenging due to the complexity of inherent protein molecular properties (i.e., net charges, polarity, molecular conformation & dimension) and sophisticated environmental parameters (i.e., biofluids), resulting in unsatisfied electrical signal resolution for proteins detection such as poor accessibility, selectivity and sensitivity. The selection of an appropriate electroanalytical approach is strongly desired which should be capable of offering easily detectable and readable signals regarding proteins particularly depending on the practical application. Herein, a molecular sandwich-based DNAzyme catalytic reaction cooperated nanopore detecting approach was designed. Especially, this approach is given the easy use of Mg2+ catalyzed DNAzyme (10-23) toward nucleic acids digestion for efficient antigen protein examination. Its applicability within the proposed strategy operates by initial formation of a molecular sandwich containing capture antibody-antigen-detection antibody for efficiently entrapment of target proteins (herein taking HIV p24 antigen for example) and immobilized on magnetic beads surface. After that, the DNAzyme was linked to the detection antibody via biotin−streptavidin interaction. In the presence of Mg2+, DNAzyme catalytic reaction was triggered to digest nucleic acids substrates and release unique cleavage fragments as reporters capable of transducing easier detectable nucleic acids as substitute of complicated and difficulty-yielded protein signals, in a nanopore. Notably, experimental validation confirms the detecting stability and sensitivity for target antigen referenced with other antigen proteins, meanwhile demonstrates the detection efficacy in human serum environment at very low concentration (LoD ~1.24 pM). This DNAzyme cooperated nanopore electroanalytical approach denotes an advancement in protein examination, may benefit in vitro test of proteinic biomarkers for disease diagnosis and prognosis assessment.