Amine Driouchi, Mason Bretan, Brynmor J Davis, Alec Heckert, Markus Seeger, Maité Bradley Silva, William S R Forrest, Jessica Hsiung, Jiongyi Tan, Hongli Yang, David T McSwiggen, Linda Song, Askhay Sule, Behnam Abaie, Hanzhe Chen, Bryant Chhun, Brianna Conroy, Liam A Elliott, Eric Gonzalez, Fedor Ilkov, Joshua Isaacs, George Labaria, Michelle Lagana, DeLaine D Larsen, Brian Margolin, Mai K Nguyen, Eugene Park, Jeremy Rine, Yangzhong Tang, Martin Vana, Andrew Wilkey, Zhengjian Zhang, Stephen Basham, Jaclyn J Ho, Stephanie Johnson, Aaron A Klammer, Kevin Lin, Xavier Darzacq, Eric Betzig, Russell T Berman, Daniel J Anderson
{"title":"Oblique line scan illumination enables expansive, accurate and sensitive single-protein measurements in solution and in living cells.","authors":"Amine Driouchi, Mason Bretan, Brynmor J Davis, Alec Heckert, Markus Seeger, Maité Bradley Silva, William S R Forrest, Jessica Hsiung, Jiongyi Tan, Hongli Yang, David T McSwiggen, Linda Song, Askhay Sule, Behnam Abaie, Hanzhe Chen, Bryant Chhun, Brianna Conroy, Liam A Elliott, Eric Gonzalez, Fedor Ilkov, Joshua Isaacs, George Labaria, Michelle Lagana, DeLaine D Larsen, Brian Margolin, Mai K Nguyen, Eugene Park, Jeremy Rine, Yangzhong Tang, Martin Vana, Andrew Wilkey, Zhengjian Zhang, Stephen Basham, Jaclyn J Ho, Stephanie Johnson, Aaron A Klammer, Kevin Lin, Xavier Darzacq, Eric Betzig, Russell T Berman, Daniel J Anderson","doi":"10.1038/s41592-025-02594-6","DOIUrl":null,"url":null,"abstract":"<p><p>An ideal tool for the study of cellular biology would enable the measure of molecular activity nondestructively within living cells. Single-molecule localization microscopy (SMLM) techniques, such as single-molecule tracking (SMT), enable in situ measurements in cells but have historically been limited by a necessary tradeoff between spatiotemporal resolution and throughput. Here we address these limitations using oblique line scan (OLS), a robust single-objective light-sheet-based illumination and detection modality that achieves nanoscale spatial resolution and sub-millisecond temporal resolution across a large field of view. We show that OLS can be used to capture protein motion up to 14 μm<sup>2</sup> s<sup>-1</sup> in living cells. We further extend the utility of OLS with in-solution SMT for single-molecule measurement of ligand-protein interactions and disruption of protein-protein interactions using purified proteins. We illustrate the versatility of OLS by showcasing two-color SMT, STORM and single-molecule fluorescence recovery after photobleaching. OLS paves the way for robust, high-throughput, single-molecule investigations of protein function required for basic research, drug screening and systems biology studies.</p>","PeriodicalId":18981,"journal":{"name":"Nature Methods","volume":" ","pages":""},"PeriodicalIF":36.1000,"publicationDate":"2025-02-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Methods","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s41592-025-02594-6","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
An ideal tool for the study of cellular biology would enable the measure of molecular activity nondestructively within living cells. Single-molecule localization microscopy (SMLM) techniques, such as single-molecule tracking (SMT), enable in situ measurements in cells but have historically been limited by a necessary tradeoff between spatiotemporal resolution and throughput. Here we address these limitations using oblique line scan (OLS), a robust single-objective light-sheet-based illumination and detection modality that achieves nanoscale spatial resolution and sub-millisecond temporal resolution across a large field of view. We show that OLS can be used to capture protein motion up to 14 μm2 s-1 in living cells. We further extend the utility of OLS with in-solution SMT for single-molecule measurement of ligand-protein interactions and disruption of protein-protein interactions using purified proteins. We illustrate the versatility of OLS by showcasing two-color SMT, STORM and single-molecule fluorescence recovery after photobleaching. OLS paves the way for robust, high-throughput, single-molecule investigations of protein function required for basic research, drug screening and systems biology studies.
期刊介绍:
Nature Methods is a monthly journal that focuses on publishing innovative methods and substantial enhancements to fundamental life sciences research techniques. Geared towards a diverse, interdisciplinary readership of researchers in academia and industry engaged in laboratory work, the journal offers new tools for research and emphasizes the immediate practical significance of the featured work. It publishes primary research papers and reviews recent technical and methodological advancements, with a particular interest in primary methods papers relevant to the biological and biomedical sciences. This includes methods rooted in chemistry with practical applications for studying biological problems.