{"title":"锥形光纤投影激光解吸/电离质谱法纳米单细胞质谱成像","authors":"Jingkai Luo, , , Heng Zhang, , , Songyan Lei, , , Yixin Leng, , , Daqing Luo, , , Yizhu Xu, , , Zhibin Yin*, , , Xiaomei Yan*, , and , Wei Hang*, ","doi":"10.1021/acs.analchem.5c04669","DOIUrl":null,"url":null,"abstract":"<p >Subcellular chemical mapping of endogenous biomolecules without labeling remains a pivotal challenge in life sciences, constrained by the limited lateral resolution and detection sensitivity of existing techniques. Herein, we report the development of tapered fiber projection laser desorption/ionization mass spectrometry (TFPLDI-MS), a new platform enabling nanoscale single-cell mass spectrometry imaging (SC-MSI). By integrating tapered fiber laser delivery with a telescopic projection system, this method achieves 570 nm lateral resolution, 400 nm imaging resolution, and a 6 amol detection limit, even at a 100 mm working distance. Exploiting enhanced ion yields from plasmonic nanoparticles, we demonstrate simultaneous nanoscale mapping of diverse exogenous drugs and endogenous phospholipids within individual cells with 400 nm pixel sizes, outperforming available laser-based SC-MSI techniques in imaging resolution, detectable analyte numbers at nanoscale sampling amounts, and operational flexibility of fiber-based sampling systems. Through spatially resolved lipidomics of HeLa cells at subcellular resolution, our TFPLDI-MSI system reveals drug-specific lipid alterations during apoptosis induced by 5-fluorouracil, paclitaxel, and cisplatin, elucidating heterogeneous therapeutic responses at the single-cell level. Crucially, the TFP system’s contamination-free operation, indefinite operational lifespan, and modular design establish the TFPLDI-MS as a transformative tool for next-generation SC-MSI techniques, bridging the gaps between nanoscale chemical imaging and biomedical applications.</p>","PeriodicalId":27,"journal":{"name":"Analytical Chemistry","volume":"97 40","pages":"22330–22340"},"PeriodicalIF":6.7000,"publicationDate":"2025-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nanoscale Single-Cell Mass Spectrometry Imaging via Tapered Fiber Projection Laser Desorption/Ionization Mass Spectrometry\",\"authors\":\"Jingkai Luo, , , Heng Zhang, , , Songyan Lei, , , Yixin Leng, , , Daqing Luo, , , Yizhu Xu, , , Zhibin Yin*, , , Xiaomei Yan*, , and , Wei Hang*, \",\"doi\":\"10.1021/acs.analchem.5c04669\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Subcellular chemical mapping of endogenous biomolecules without labeling remains a pivotal challenge in life sciences, constrained by the limited lateral resolution and detection sensitivity of existing techniques. Herein, we report the development of tapered fiber projection laser desorption/ionization mass spectrometry (TFPLDI-MS), a new platform enabling nanoscale single-cell mass spectrometry imaging (SC-MSI). By integrating tapered fiber laser delivery with a telescopic projection system, this method achieves 570 nm lateral resolution, 400 nm imaging resolution, and a 6 amol detection limit, even at a 100 mm working distance. Exploiting enhanced ion yields from plasmonic nanoparticles, we demonstrate simultaneous nanoscale mapping of diverse exogenous drugs and endogenous phospholipids within individual cells with 400 nm pixel sizes, outperforming available laser-based SC-MSI techniques in imaging resolution, detectable analyte numbers at nanoscale sampling amounts, and operational flexibility of fiber-based sampling systems. Through spatially resolved lipidomics of HeLa cells at subcellular resolution, our TFPLDI-MSI system reveals drug-specific lipid alterations during apoptosis induced by 5-fluorouracil, paclitaxel, and cisplatin, elucidating heterogeneous therapeutic responses at the single-cell level. Crucially, the TFP system’s contamination-free operation, indefinite operational lifespan, and modular design establish the TFPLDI-MS as a transformative tool for next-generation SC-MSI techniques, bridging the gaps between nanoscale chemical imaging and biomedical applications.</p>\",\"PeriodicalId\":27,\"journal\":{\"name\":\"Analytical Chemistry\",\"volume\":\"97 40\",\"pages\":\"22330–22340\"},\"PeriodicalIF\":6.7000,\"publicationDate\":\"2025-10-04\",\"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.5c04669\",\"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://pubs.acs.org/doi/10.1021/acs.analchem.5c04669","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Nanoscale Single-Cell Mass Spectrometry Imaging via Tapered Fiber Projection Laser Desorption/Ionization Mass Spectrometry
Subcellular chemical mapping of endogenous biomolecules without labeling remains a pivotal challenge in life sciences, constrained by the limited lateral resolution and detection sensitivity of existing techniques. Herein, we report the development of tapered fiber projection laser desorption/ionization mass spectrometry (TFPLDI-MS), a new platform enabling nanoscale single-cell mass spectrometry imaging (SC-MSI). By integrating tapered fiber laser delivery with a telescopic projection system, this method achieves 570 nm lateral resolution, 400 nm imaging resolution, and a 6 amol detection limit, even at a 100 mm working distance. Exploiting enhanced ion yields from plasmonic nanoparticles, we demonstrate simultaneous nanoscale mapping of diverse exogenous drugs and endogenous phospholipids within individual cells with 400 nm pixel sizes, outperforming available laser-based SC-MSI techniques in imaging resolution, detectable analyte numbers at nanoscale sampling amounts, and operational flexibility of fiber-based sampling systems. Through spatially resolved lipidomics of HeLa cells at subcellular resolution, our TFPLDI-MSI system reveals drug-specific lipid alterations during apoptosis induced by 5-fluorouracil, paclitaxel, and cisplatin, elucidating heterogeneous therapeutic responses at the single-cell level. Crucially, the TFP system’s contamination-free operation, indefinite operational lifespan, and modular design establish the TFPLDI-MS as a transformative tool for next-generation SC-MSI techniques, bridging the gaps between nanoscale chemical imaging and biomedical applications.
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.