Yuan Wei, Lei Zheng, Zhiwei Hu, Liang Shen, Jianwei Jiao, Jin Jiao, Yuna Guo
{"title":"电子穿梭机制驱动接近标记从临床样本揭示卵巢癌肿瘤标志物特征","authors":"Yuan Wei, Lei Zheng, Zhiwei Hu, Liang Shen, Jianwei Jiao, Jin Jiao, Yuna Guo","doi":"10.1021/acs.analchem.5c04168","DOIUrl":null,"url":null,"abstract":"In this study, we presented a revolutionary proximity labeling platform, MOF-HRP-Apt, which for the first time integrated electron mediation into the horseradish peroxidase (HRP)-catalyzed proximity labeling system. This novel strategy enabled a single molecular recognition event into multiple covalent labeling events, amplifying spatial signals and enhancing detection sensitivity of the tumor biomarker PTK7. The platform utilized the redox-active iron-based metal–organic framework (MOF) material NH<sub>2</sub>-MIL-88B, whose Fe<sup>2+</sup>/Fe<sup>3+</sup> redox center facilitated electron transfer to the active site of HRP, dramatically boosting HRP’s catalytic activity toward phenol oxidation and accelerating phenoxo radical generation. These radicals could covalently label tyrosine residues in PTK7 and its adjacent proteins to achieve efficient spatial localization. Compared to conventional HRP-Apt strategies, MOF-HRP-Apt platform exhibited significantly stronger labeling signals (1.74-3 folds increase) and improved signal-to-noise ratios (1.93−2.2 folds enhancement) in cellular models. It maintained robust performance even under challenging conditions of low PTK7 expression, siRNA-mediated knockdown, or paclitaxel-induced suppression. Moreover, in clinical tissue specimens, our platform successfully enabled stratified PTK7 visualization across the ovarian cancer progression spectrum─from normal tissue through early to advanced stages, demonstrating its exceptional sensitivity and adaptability in complex biological environments. By combining target-specific recognition with signal amplification, this strategy offered the ultrasensitive detection of low-abundance biomarkers. With its remarkable potential for early cancer screening, real-time molecular tracking, and personalized therapeutic development, our platform represents a significant leap forward in molecular diagnostics. This study exemplifies the transformative power of electron-mediated proximity labeling, offering a promising avenue for advancing precision medicine and molecular biology.","PeriodicalId":27,"journal":{"name":"Analytical Chemistry","volume":"952 1","pages":""},"PeriodicalIF":6.7000,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Electron-Shuttling Mechanisms Drive Proximity Labeling to Unveil Tumor Marker Characteristics in Ovarian Cancer from Clinical Samples\",\"authors\":\"Yuan Wei, Lei Zheng, Zhiwei Hu, Liang Shen, Jianwei Jiao, Jin Jiao, Yuna Guo\",\"doi\":\"10.1021/acs.analchem.5c04168\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this study, we presented a revolutionary proximity labeling platform, MOF-HRP-Apt, which for the first time integrated electron mediation into the horseradish peroxidase (HRP)-catalyzed proximity labeling system. This novel strategy enabled a single molecular recognition event into multiple covalent labeling events, amplifying spatial signals and enhancing detection sensitivity of the tumor biomarker PTK7. The platform utilized the redox-active iron-based metal–organic framework (MOF) material NH<sub>2</sub>-MIL-88B, whose Fe<sup>2+</sup>/Fe<sup>3+</sup> redox center facilitated electron transfer to the active site of HRP, dramatically boosting HRP’s catalytic activity toward phenol oxidation and accelerating phenoxo radical generation. These radicals could covalently label tyrosine residues in PTK7 and its adjacent proteins to achieve efficient spatial localization. Compared to conventional HRP-Apt strategies, MOF-HRP-Apt platform exhibited significantly stronger labeling signals (1.74-3 folds increase) and improved signal-to-noise ratios (1.93−2.2 folds enhancement) in cellular models. It maintained robust performance even under challenging conditions of low PTK7 expression, siRNA-mediated knockdown, or paclitaxel-induced suppression. Moreover, in clinical tissue specimens, our platform successfully enabled stratified PTK7 visualization across the ovarian cancer progression spectrum─from normal tissue through early to advanced stages, demonstrating its exceptional sensitivity and adaptability in complex biological environments. By combining target-specific recognition with signal amplification, this strategy offered the ultrasensitive detection of low-abundance biomarkers. With its remarkable potential for early cancer screening, real-time molecular tracking, and personalized therapeutic development, our platform represents a significant leap forward in molecular diagnostics. This study exemplifies the transformative power of electron-mediated proximity labeling, offering a promising avenue for advancing precision medicine and molecular biology.\",\"PeriodicalId\":27,\"journal\":{\"name\":\"Analytical Chemistry\",\"volume\":\"952 1\",\"pages\":\"\"},\"PeriodicalIF\":6.7000,\"publicationDate\":\"2025-10-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Analytical Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.analchem.5c04168\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.analchem.5c04168","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Electron-Shuttling Mechanisms Drive Proximity Labeling to Unveil Tumor Marker Characteristics in Ovarian Cancer from Clinical Samples
In this study, we presented a revolutionary proximity labeling platform, MOF-HRP-Apt, which for the first time integrated electron mediation into the horseradish peroxidase (HRP)-catalyzed proximity labeling system. This novel strategy enabled a single molecular recognition event into multiple covalent labeling events, amplifying spatial signals and enhancing detection sensitivity of the tumor biomarker PTK7. The platform utilized the redox-active iron-based metal–organic framework (MOF) material NH2-MIL-88B, whose Fe2+/Fe3+ redox center facilitated electron transfer to the active site of HRP, dramatically boosting HRP’s catalytic activity toward phenol oxidation and accelerating phenoxo radical generation. These radicals could covalently label tyrosine residues in PTK7 and its adjacent proteins to achieve efficient spatial localization. Compared to conventional HRP-Apt strategies, MOF-HRP-Apt platform exhibited significantly stronger labeling signals (1.74-3 folds increase) and improved signal-to-noise ratios (1.93−2.2 folds enhancement) in cellular models. It maintained robust performance even under challenging conditions of low PTK7 expression, siRNA-mediated knockdown, or paclitaxel-induced suppression. Moreover, in clinical tissue specimens, our platform successfully enabled stratified PTK7 visualization across the ovarian cancer progression spectrum─from normal tissue through early to advanced stages, demonstrating its exceptional sensitivity and adaptability in complex biological environments. By combining target-specific recognition with signal amplification, this strategy offered the ultrasensitive detection of low-abundance biomarkers. With its remarkable potential for early cancer screening, real-time molecular tracking, and personalized therapeutic development, our platform represents a significant leap forward in molecular diagnostics. This study exemplifies the transformative power of electron-mediated proximity labeling, offering a promising avenue for advancing precision medicine and molecular biology.
期刊介绍:
Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.