Zhitao Zhao, , , Yanting Guo, , , Kellye A. Cupp-Sutton, , , Zhige Wang, , , Xiaowen Liu, , and , Si Wu*,
{"title":"使用多段喷雾-毛细管CE-MS对picogram复杂样品进行高通量自上而下的蛋白质组学分析。","authors":"Zhitao Zhao, , , Yanting Guo, , , Kellye A. Cupp-Sutton, , , Zhige Wang, , , Xiaowen Liu, , and , Si Wu*, ","doi":"10.1021/acs.analchem.5c02334","DOIUrl":null,"url":null,"abstract":"<p >Ultrasensitive top-down proteomics techniques provide valuable insights into PTM-regulated cellular functions in mass-limited samples. Capillary electrophoresis (CE) is a promising separation technique for top-down proteomics due to its high resolution, high sensitivity, and short cycle times compared to traditional liquid chromatography (LC)-based methods. We recently developed the “Spray-Capillary,” an ESI-assisted device for quantitative ultralow-volume sampling and online CE-MS analysis, which successfully characterized hundreds of intact proteoforms from picogram-level cell lysate samples and showed promise for quantitative analysis of mass-limited complex biological samples. In this study, we further improved throughput for mass-limited top-down proteomics by integrating multisegment sample injection with our spray-capillary CE-MS analysis platform. By optimizing the spacer between sample plugs, we enabled the injection of multiple samples into the spray-capillary prior to a single CE-MS analysis, achieving baseline separation of identical proteins from different segments. Under optimized conditions, we quantified<i>E. coli</i>lysate (10–250 pg) using a six-point calibration curve in a single analysis (e.g., ∼60 min run time), yielding a strong linear correlation (<i>R</i><sup>2</sup> > 0.98). Our method supports up to 17 sample segments per run (e.g., ∼90 min run time) while maintaining baseline separation. This optimized multisegment injection platform has the potential to analyze hundreds of mass-limited samples (e.g., single cells) per day, significantly enhancing throughput in top-down proteomics.</p>","PeriodicalId":27,"journal":{"name":"Analytical Chemistry","volume":"97 41","pages":"22482–22489"},"PeriodicalIF":6.7000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"High-Throughput Top-Down Proteomic Analysis of Picogram-Level Complex Samples Using Multisegment Spray-Capillary CE-MS\",\"authors\":\"Zhitao Zhao, , , Yanting Guo, , , Kellye A. Cupp-Sutton, , , Zhige Wang, , , Xiaowen Liu, , and , Si Wu*, \",\"doi\":\"10.1021/acs.analchem.5c02334\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Ultrasensitive top-down proteomics techniques provide valuable insights into PTM-regulated cellular functions in mass-limited samples. Capillary electrophoresis (CE) is a promising separation technique for top-down proteomics due to its high resolution, high sensitivity, and short cycle times compared to traditional liquid chromatography (LC)-based methods. We recently developed the “Spray-Capillary,” an ESI-assisted device for quantitative ultralow-volume sampling and online CE-MS analysis, which successfully characterized hundreds of intact proteoforms from picogram-level cell lysate samples and showed promise for quantitative analysis of mass-limited complex biological samples. In this study, we further improved throughput for mass-limited top-down proteomics by integrating multisegment sample injection with our spray-capillary CE-MS analysis platform. By optimizing the spacer between sample plugs, we enabled the injection of multiple samples into the spray-capillary prior to a single CE-MS analysis, achieving baseline separation of identical proteins from different segments. Under optimized conditions, we quantified<i>E. coli</i>lysate (10–250 pg) using a six-point calibration curve in a single analysis (e.g., ∼60 min run time), yielding a strong linear correlation (<i>R</i><sup>2</sup> > 0.98). Our method supports up to 17 sample segments per run (e.g., ∼90 min run time) while maintaining baseline separation. This optimized multisegment injection platform has the potential to analyze hundreds of mass-limited samples (e.g., single cells) per day, significantly enhancing throughput in top-down proteomics.</p>\",\"PeriodicalId\":27,\"journal\":{\"name\":\"Analytical Chemistry\",\"volume\":\"97 41\",\"pages\":\"22482–22489\"},\"PeriodicalIF\":6.7000,\"publicationDate\":\"2025-10-01\",\"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.5c02334\",\"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.5c02334","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
High-Throughput Top-Down Proteomic Analysis of Picogram-Level Complex Samples Using Multisegment Spray-Capillary CE-MS
Ultrasensitive top-down proteomics techniques provide valuable insights into PTM-regulated cellular functions in mass-limited samples. Capillary electrophoresis (CE) is a promising separation technique for top-down proteomics due to its high resolution, high sensitivity, and short cycle times compared to traditional liquid chromatography (LC)-based methods. We recently developed the “Spray-Capillary,” an ESI-assisted device for quantitative ultralow-volume sampling and online CE-MS analysis, which successfully characterized hundreds of intact proteoforms from picogram-level cell lysate samples and showed promise for quantitative analysis of mass-limited complex biological samples. In this study, we further improved throughput for mass-limited top-down proteomics by integrating multisegment sample injection with our spray-capillary CE-MS analysis platform. By optimizing the spacer between sample plugs, we enabled the injection of multiple samples into the spray-capillary prior to a single CE-MS analysis, achieving baseline separation of identical proteins from different segments. Under optimized conditions, we quantifiedE. colilysate (10–250 pg) using a six-point calibration curve in a single analysis (e.g., ∼60 min run time), yielding a strong linear correlation (R2 > 0.98). Our method supports up to 17 sample segments per run (e.g., ∼90 min run time) while maintaining baseline separation. This optimized multisegment injection platform has the potential to analyze hundreds of mass-limited samples (e.g., single cells) per day, significantly enhancing throughput in top-down proteomics.
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.