锥形光纤投影激光解吸/电离质谱法纳米单细胞质谱成像

IF 6.7 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Jingkai Luo, , , Heng Zhang, , , Songyan Lei, , , Yixin Leng, , , Daqing Luo, , , Yizhu Xu, , , Zhibin Yin*, , , Xiaomei Yan*, , and , Wei Hang*, 
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引用次数: 0

摘要

由于现有技术的横向分辨率和检测灵敏度有限,内源性生物分子的亚细胞化学作图仍然是生命科学中的一个关键挑战。在此,我们报告了锥形光纤投影激光解吸/电离质谱(TFPLDI-MS)的发展,这是一种新的纳米单细胞质谱成像(SC-MSI)平台。通过将锥形光纤激光传输与伸缩投影系统集成,该方法即使在100 mm的工作距离下也能实现570 nm的横向分辨率、400 nm的成像分辨率和6 amol的检测极限。利用等离子体纳米粒子提高离子产量,我们展示了400纳米像素尺寸的单个细胞内多种外源性药物和内源性磷脂的同时纳米尺度定位,在成像分辨率、纳米尺度采样量下可检测的分析物数量和基于纤维的采样系统的操作灵活性方面优于现有的基于激光的SC-MSI技术。我们的TFPLDI-MSI系统通过亚细胞分辨率的HeLa细胞的空间分辨脂质组学,揭示了5-氟尿嘧啶、紫杉醇和顺铂诱导的细胞凋亡过程中药物特异性脂质改变,阐明了单细胞水平上的异质性治疗反应。至关重要的是,TFP系统的无公害操作、无限使用寿命和模块化设计使TFPLDI-MS成为下一代SC-MSI技术的变革工具,弥合了纳米级化学成像和生物医学应用之间的差距。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Nanoscale Single-Cell Mass Spectrometry Imaging via Tapered Fiber Projection Laser Desorption/Ionization Mass Spectrometry

Nanoscale Single-Cell Mass Spectrometry Imaging via Tapered Fiber Projection Laser Desorption/Ionization Mass Spectrometry

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.

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来源期刊
Analytical Chemistry
Analytical Chemistry 化学-分析化学
CiteScore
12.10
自引率
12.20%
发文量
1949
审稿时长
1.4 months
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.
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