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本文引用的文献

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Identification and Imaging of N Labeled Cells with ToF-SIMS.用飞行时间二次离子质谱法对N标记细胞进行鉴定与成像
Surf Interface Anal. 2011 Jan;43(1-2):336-339. doi: 10.1002/sia.3679.
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Multi-isotope imaging mass spectrometry quantifies stem cell division and metabolism.多同位素成像质谱定量分析干细胞分裂和代谢。
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3
Multi-isotope imaging mass spectrometry reveals slow protein turnover in hair-cell stereocilia.多同位素成像质谱法揭示了毛细胞静纤毛中缓慢的蛋白质周转。
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Identifying individual cell types in heterogeneous cultures using secondary ion mass spectrometry imaging with C60 etching and multivariate analysis.利用 C60 刻蚀和多元分析的二次离子质谱成像技术鉴定异质培养中的单个细胞类型。
Anal Chem. 2012 Jan 17;84(2):893-900. doi: 10.1021/ac201179t. Epub 2012 Jan 3.
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C60 secondary ion Fourier transform ion cyclotron resonance mass spectrometry.C60 二次离子傅里叶变换离子回旋共振质谱法。
Anal Chem. 2011 Dec 15;83(24):9552-6. doi: 10.1021/ac2023348. Epub 2011 Nov 18.
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ToF-SIMS imaging and depth profiling of HeLa cells treated with bromodeoxyuridine.用溴脱氧尿苷处理的HeLa细胞的飞行时间二次离子质谱成像和深度剖析。
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Stretched tissue mounting for MALDI mass spectrometry imaging.拉伸组织安装用于 MALDI 质谱成像。
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9
Analysis of native biological surfaces using a 100 kV massive gold cluster source.使用 100kV 大规模金团簇源分析天然生物表面。
Anal Chem. 2011 Nov 15;83(22):8448-53. doi: 10.1021/ac201481r. Epub 2011 Oct 18.
10
Imaging mass spectrometry in microbiology.微生物成像质谱技术。
Nat Rev Microbiol. 2011 Aug 8;9(9):683-94. doi: 10.1038/nrmicro2634.

单细胞的质谱成像和分析。

Mass spectrometry imaging and profiling of single cells.

机构信息

Department of Chemistry and the Beckman Institute of Science and Technology, University of Illinois, Urbana IL 61801, USA.

Department of Chemistry and the Beckman Institute of Science and Technology, University of Illinois, Urbana IL 61801, USA.

出版信息

J Proteomics. 2012 Aug 30;75(16):5036-5051. doi: 10.1016/j.jprot.2012.03.017. Epub 2012 Mar 29.

DOI:10.1016/j.jprot.2012.03.017
PMID:22498881
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3419297/
Abstract

Mass spectrometry imaging and profiling of individual cells and subcellular structures provide unique analytical capabilities for biological and biomedical research, including determination of the biochemical heterogeneity of cellular populations and intracellular localization of pharmaceuticals. Two mass spectrometry technologies-secondary ion mass spectrometry (SIMS) and matrix assisted laser desorption/ionization mass spectrometry (MALDI MS)-are most often used in micro-bioanalytical investigations. Recent advances in ion probe technologies have increased the dynamic range and sensitivity of analyte detection by SIMS, allowing two- and three-dimensional localization of analytes in a variety of cells. SIMS operating in the mass spectrometry imaging (MSI) mode can routinely reach spatial resolutions at the submicron level; therefore, it is frequently used in studies of the chemical composition of subcellular structures. MALDI MS offers a large mass range and high sensitivity of analyte detection. It has been successfully applied in a variety of single-cell and organelle profiling studies. Innovative instrumentation such as scanning microprobe MALDI and mass microscope spectrometers enables new subcellular MSI measurements. Other approaches for MS-based chemical imaging and profiling include those based on near-field laser ablation and inductively-coupled plasma MS analysis, which offer complementary capabilities for subcellular chemical imaging and profiling.

摘要

质谱成像和单个细胞及亚细胞结构分析为生物和生物医学研究提供了独特的分析能力,包括确定细胞群体的生化异质性和药物的细胞内定位。两种质谱技术——二次离子质谱(SIMS)和基质辅助激光解吸/电离质谱(MALDI MS)——最常用于微分析研究。离子探针技术的最新进展提高了 SIMS 分析物检测的动态范围和灵敏度,允许在各种细胞中对分析物进行二维和三维定位。以质谱成像(MSI)模式工作的 SIMS 通常可以达到亚微米级别的空间分辨率;因此,它常用于亚细胞结构化学成分的研究。MALDI MS 提供了大的质量范围和高的分析物检测灵敏度。它已成功应用于各种单细胞和细胞器分析研究中。扫描微探针 MALDI 和质谱显微镜等创新仪器使新的亚细胞 MSI 测量成为可能。基于近场激光烧蚀和电感耦合等离子体质谱分析的其他基于 MS 的化学成像和分析方法为亚细胞化学成像和分析提供了互补能力。