SpotOn: A Tool to Enhance Echo Acoustic Standard Deposition for Quantitative Mass Spectrometry Imaging

IF 6.7
Chemical & Biomedical Imaging Pub Date : 2026-09-28 Epub Date: 2026-07-22 DOI:10.1021/cbmi.6c00010
Emily R. Sekera, Nathaniel Twarog, Rebekah DeVries, P. Jake Slavish, John J. Bowling, Anang A. Shelat
{"title":"SpotOn: A Tool to Enhance Echo Acoustic Standard Deposition for Quantitative Mass Spectrometry Imaging","authors":"Emily R. Sekera,&nbsp;Nathaniel Twarog,&nbsp;Rebekah DeVries,&nbsp;P. Jake Slavish,&nbsp;John J. Bowling,&nbsp;Anang A. Shelat","doi":"10.1021/cbmi.6c00010","DOIUrl":null,"url":null,"abstract":"<p>The quantitative evaluation of therapeutics in the drug\r\ndiscovery\r\npipeline is essential for elucidating their pharmacokinetic and pharmacodynamic\r\nprofiles within complex biological systems. Traditionally, autoradiography\r\nand liquid chromatography-mass spectrometry (LC-MS) have been employed\r\nfor such analyses. However, matrix-assisted laser desorption ionization\r\nmass spectrometry imaging (MALDI-MSI) is emerging as a promising alternative,\r\noffering a more rapid untargeted workflow. Quantitative MALDI-MSI\r\n(qMSI) relies on accurate calibration to achieve robust and reproducible\r\nquantification of analytes. Here, we present an open-source software\r\ntool, SpotOn, designed to facilitate the discrete deposition of low-volume\r\ncalibration standards onto glass slides or tissue sections. By enabling\r\nprecise placement and significantly reducing the volume of standards\r\nrequired, our tool affords the generation of more calibration points\r\nacross a wider dynamic range, thereby improving the robustness and\r\naccuracy of quantitative analyses. Software was validated using JQ1\r\non both glass slides and murine liver tissue. The resulting calibration\r\ncurves demonstrated strong linearity, with coefficients of determination\r\n(<em>R</em><sup>2</sup>) exceeding 0.92. This tool streamlines\r\nthe qMSI workflow, conserves valuable reagents, and enhances analytical\r\nreliability, making it a helpful resource.</p>","PeriodicalId":53181,"journal":{"name":"Chemical & Biomedical Imaging","volume":"4 9","pages":"2119–2125"},"PeriodicalIF":6.7000,"publicationDate":"2026-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical & Biomedical Imaging","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/cbmi.6c00010","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/7/22 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The quantitative evaluation of therapeutics in the drug discovery pipeline is essential for elucidating their pharmacokinetic and pharmacodynamic profiles within complex biological systems. Traditionally, autoradiography and liquid chromatography-mass spectrometry (LC-MS) have been employed for such analyses. However, matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI-MSI) is emerging as a promising alternative, offering a more rapid untargeted workflow. Quantitative MALDI-MSI (qMSI) relies on accurate calibration to achieve robust and reproducible quantification of analytes. Here, we present an open-source software tool, SpotOn, designed to facilitate the discrete deposition of low-volume calibration standards onto glass slides or tissue sections. By enabling precise placement and significantly reducing the volume of standards required, our tool affords the generation of more calibration points across a wider dynamic range, thereby improving the robustness and accuracy of quantitative analyses. Software was validated using JQ1 on both glass slides and murine liver tissue. The resulting calibration curves demonstrated strong linearity, with coefficients of determination (R2) exceeding 0.92. This tool streamlines the qMSI workflow, conserves valuable reagents, and enhances analytical reliability, making it a helpful resource.

SpotOn:一种增强定量质谱成像回声声学标准沉积的工具
药物发现管道中的治疗方法的定量评估对于阐明其在复杂生物系统中的药代动力学和药效学特征至关重要。传统上,自放射法和液相色谱-质谱法(LC-MS)已被用于这类分析。然而,基质辅助激光解吸电离质谱成像(MALDI-MSI)正在成为一种有前途的替代方案,提供了更快速的非靶向工作流程。定量MALDI-MSI(qMSI)依靠准确的校准来实现分析物的稳健和可重复性定量。在这里,我们提出了一个开源软件工具,SpotOn,旨在促进在玻璃载玻片或组织切片上离散沉积小体积校准标准。通过实现精确放置并显着减少所需标准的体积,我们的工具可以在更宽的动态范围内生成更多的校准点,从而提高定量分析的稳健性和准确性。软件使用jq11在玻片和小鼠肝组织上进行验证。标定曲线线性关系良好,决定系数(R2)均大于0.92。该工具简化了qMSI工作流程,保存了有价值的试剂,并提高了分析的可靠性,使其成为有用的资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Chemical & Biomedical Imaging
Chemical & Biomedical Imaging 化学与生物成像-
CiteScore
1.00
自引率
0.00%
发文量
0
期刊介绍: Chemical & Biomedical Imaging is a peer-reviewed open access journal devoted to the publication of cutting-edge research papers on all aspects of chemical and biomedical imaging. This interdisciplinary field sits at the intersection of chemistry physics biology materials engineering and medicine. The journal aims to bring together researchers from across these disciplines to address cutting-edge challenges of fundamental research and applications.Topics of particular interest include but are not limited to:Imaging of processes and reactionsImaging of nanoscale microscale and mesoscale materialsImaging of biological interactions and interfacesSingle-molecule and cellular imagingWhole-organ and whole-body imagingMolecular imaging probes and contrast agentsBioluminescence chemiluminescence and electrochemiluminescence imagingNanophotonics and imagingChemical tools for new imaging modalitiesChemical and imaging techniques in diagnosis and therapyImaging-guided drug deliveryAI and machine learning assisted imaging
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书