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基于纳米光子学的质谱分析用于痕量和单细胞分析。

Nanophotonic ionization for ultratrace and single-cell analysis by mass spectrometry.

机构信息

W. M. Keck Institute for Proteomics Technology and Applications, Department of Chemistry, The George Washington University, Washington, District of Columbia 20052, United States.

出版信息

Anal Chem. 2012 Sep 18;84(18):7756-62. doi: 10.1021/ac301238k. Epub 2012 Aug 24.

Abstract

Recent mechanistic studies have indicated that at subwavelength post diameters and selected aspect ratios nanopost arrays (NAPA) exhibit ion yield resonances ( Walker , B. N. , Stolee , J. A. , Pickel , D. L. , Retterer , S. T. , and Vertes , A. J. Phys. Chem. C 2010 , 114 , 4835 - 4840 ). In this contribution we explore the analytical utility of these optimized structures as matrix-free platforms for laser desorption ionization mass spectrometry (LDI-MS). Using NAPA, we show that high ionization efficiencies enable the detection of ultratrace amounts of analytes (e.g., ∼800 zmol of verapamil) with a dynamic range spanning up to 4 orders of magnitude. Due to the clean nanofabrication process and the lack of matrix material, minimal background interferences are present in the low-mass range. We demonstrate that LDI from NAPA ionizes a broad class of small molecules including pharmaceuticals, natural products, metabolites, and explosives. Quantitation of resveratrol in red wine samples shows that the analysis of targeted analytes in complex mixtures is feasible with minimal sample preparation using NAPA-based LDI. We also describe how multiple metabolite species can be directly detected in single yeast cells deposited on the NAPA chip. Twenty-four metabolites, or 4% of the yeast metabolome, were identified in the single-cell spectra.

摘要

最近的机制研究表明,在亚波长后直径和选定的纵横比下,纳米柱阵列(NAPA)表现出离子产额共振(Walker,B. N.,Stolee,J. A.,Pickel,D. L.,Retterer,S. T.,和Vertes,A. J. Phys. Chem. C 2010,114,4835-4840)。在本贡献中,我们探索了这些优化结构作为无基质平台用于激光解吸电离质谱(LDI-MS)的分析效用。使用 NAPA,我们表明,高离化效率使得能够检测痕量分析物(例如,维拉帕米的约 800 zmol),其动态范围跨越多达 4 个数量级。由于清洁的纳米制造工艺和缺乏基质材料,在低质量范围内存在最小的背景干扰。我们证明,NAPA 的 LDI 可以使包括药物、天然产物、代谢物和爆炸物在内的广泛的小分子离化。在红酒样品中对白藜芦醇的定量分析表明,使用基于 NAPA 的 LDI 进行最小样品制备即可实现复杂混合物中靶向分析物的分析。我们还描述了如何直接在沉积在 NAPA 芯片上的单个酵母细胞中检测多种代谢物。在单细胞光谱中鉴定出 24 种代谢物,即酵母代谢组的 4%。

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