Mengnan Wang, Guangsheng Ge, Xueyi Fan, Kai Zheng, Yuxin Miao, Qing Yao, Min Ma, Jianlong Wang, Yanru Wang
{"title":"基于纳米体和天然荧光探针的机器学习驱动双模式免疫分析用于铜绿假单胞菌的超灵敏定量","authors":"Mengnan Wang, Guangsheng Ge, Xueyi Fan, Kai Zheng, Yuxin Miao, Qing Yao, Min Ma, Jianlong Wang, Yanru Wang","doi":"10.1021/acs.analchem.6c04879","DOIUrl":null,"url":null,"abstract":"<p><em>Pseudomonas aeruginosa</em> is a Gram-negative\r\nopportunistic\r\nbacterial pathogen posing severe threat to environmental safety and\r\nhuman health. To achieve rapid and accurate detection, we developed\r\na nanobody-based colorimetric-fluorescent dual-mode sandwich immunosensor\r\nusing natural fluorescent probe and further integrated machine learning\r\nto enhance the signal readout and improve detection sensitivity. Here,\r\nspecific nanobodies toward <em>P. aeruginosa</em> were successfully\r\ndeveloped for the first time by biopanning against an immune phage-displayed\r\nnanobody library. Natural fluorescent quinine, which possesses intrinsic\r\nfluorescence and undergoes fluorescence quenching via an internal\r\nquenching effect, was employed as the fluorescent probe. With the\r\nbaseline LODs obtained by direct fitting of the raw optical signals\r\n(9.005 × 10<sup>5</sup> CFU/mL for colorimetry and 3.02 ×\r\n10<sup>3</sup> CFU/mL for fluorescence), an XGBoost model was introduced\r\nand further reduces the LOD to 3.269 × 10<sup>3</sup> CFU/mL\r\nand 3.96 × 10<sup>2</sup> CFU/mL, achieving a 275-fold and 7.6-fold\r\nimprovement in sensitivity, respectively. Furthermore, following a\r\nbrief pre-enrichment, this method enables detection of <em>P. aeruginosa</em> at concentrations as low as 10 CFU/mL. Recoveries\r\nin water samples ranged from 81.47% to 119.47%, with a coefficient\r\nof variation below 8.44%, showing good agreement with machine learning\r\npredictions (<em>R</em><sup>2</sup> = 0.957). No cross-reactivity\r\nwas observed with closely related or heterologous bacteria. This method\r\nprovides a technical approach for the precise quantitative monitoring\r\nof <em>P. aeruginosa</em> in complex environments.</p>","PeriodicalId":27,"journal":{"name":"Analytical Chemistry","volume":"98 41","pages":"29700–29712"},"PeriodicalIF":7.3000,"publicationDate":"2026-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Machine-Learning-Driven Dual-Mode Immunoassay Based on Nanobody and Natural Fluorescent Probe for Ultrasensitive Quantification of Pseudomonas aeruginosa\",\"authors\":\"Mengnan Wang, Guangsheng Ge, Xueyi Fan, Kai Zheng, Yuxin Miao, Qing Yao, Min Ma, Jianlong Wang, Yanru Wang\",\"doi\":\"10.1021/acs.analchem.6c04879\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><em>Pseudomonas aeruginosa</em> is a Gram-negative\\r\\nopportunistic\\r\\nbacterial pathogen posing severe threat to environmental safety and\\r\\nhuman health. To achieve rapid and accurate detection, we developed\\r\\na nanobody-based colorimetric-fluorescent dual-mode sandwich immunosensor\\r\\nusing natural fluorescent probe and further integrated machine learning\\r\\nto enhance the signal readout and improve detection sensitivity. Here,\\r\\nspecific nanobodies toward <em>P. aeruginosa</em> were successfully\\r\\ndeveloped for the first time by biopanning against an immune phage-displayed\\r\\nnanobody library. Natural fluorescent quinine, which possesses intrinsic\\r\\nfluorescence and undergoes fluorescence quenching via an internal\\r\\nquenching effect, was employed as the fluorescent probe. With the\\r\\nbaseline LODs obtained by direct fitting of the raw optical signals\\r\\n(9.005 × 10<sup>5</sup> CFU/mL for colorimetry and 3.02 ×\\r\\n10<sup>3</sup> CFU/mL for fluorescence), an XGBoost model was introduced\\r\\nand further reduces the LOD to 3.269 × 10<sup>3</sup> CFU/mL\\r\\nand 3.96 × 10<sup>2</sup> CFU/mL, achieving a 275-fold and 7.6-fold\\r\\nimprovement in sensitivity, respectively. Furthermore, following a\\r\\nbrief pre-enrichment, this method enables detection of <em>P. aeruginosa</em> at concentrations as low as 10 CFU/mL. Recoveries\\r\\nin water samples ranged from 81.47% to 119.47%, with a coefficient\\r\\nof variation below 8.44%, showing good agreement with machine learning\\r\\npredictions (<em>R</em><sup>2</sup> = 0.957). No cross-reactivity\\r\\nwas observed with closely related or heterologous bacteria. This method\\r\\nprovides a technical approach for the precise quantitative monitoring\\r\\nof <em>P. aeruginosa</em> in complex environments.</p>\",\"PeriodicalId\":27,\"journal\":{\"name\":\"Analytical Chemistry\",\"volume\":\"98 41\",\"pages\":\"29700–29712\"},\"PeriodicalIF\":7.3000,\"publicationDate\":\"2026-10-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Analytical Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.analchem.6c04879\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2026/10/6 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.analchem.6c04879","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/10/6 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Machine-Learning-Driven Dual-Mode Immunoassay Based on Nanobody and Natural Fluorescent Probe for Ultrasensitive Quantification of Pseudomonas aeruginosa
Pseudomonas aeruginosa is a Gram-negative
opportunistic
bacterial pathogen posing severe threat to environmental safety and
human health. To achieve rapid and accurate detection, we developed
a nanobody-based colorimetric-fluorescent dual-mode sandwich immunosensor
using natural fluorescent probe and further integrated machine learning
to enhance the signal readout and improve detection sensitivity. Here,
specific nanobodies toward P. aeruginosa were successfully
developed for the first time by biopanning against an immune phage-displayed
nanobody library. Natural fluorescent quinine, which possesses intrinsic
fluorescence and undergoes fluorescence quenching via an internal
quenching effect, was employed as the fluorescent probe. With the
baseline LODs obtained by direct fitting of the raw optical signals
(9.005 × 105 CFU/mL for colorimetry and 3.02 ×
103 CFU/mL for fluorescence), an XGBoost model was introduced
and further reduces the LOD to 3.269 × 103 CFU/mL
and 3.96 × 102 CFU/mL, achieving a 275-fold and 7.6-fold
improvement in sensitivity, respectively. Furthermore, following a
brief pre-enrichment, this method enables detection of P. aeruginosa at concentrations as low as 10 CFU/mL. Recoveries
in water samples ranged from 81.47% to 119.47%, with a coefficient
of variation below 8.44%, showing good agreement with machine learning
predictions (R2 = 0.957). No cross-reactivity
was observed with closely related or heterologous bacteria. This method
provides a technical approach for the precise quantitative monitoring
of P. aeruginosa in complex environments.
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.