4.8 Article

Nanophotonic Ionization for Ultratrace and Single-Cell Analysis by Mass Spectrometry

Journal

ANALYTICAL CHEMISTRY
Volume 84, Issue 18, Pages 7756-7762

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ac301238k

Keywords

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Funding

  1. Chemical Sciences, Geosciences and Biosciences Division, Office of Basic Energy Sciences, Office of Science, U.S. Department of Energy [DE-FG02-01ER15129]
  2. George Washington University Selective Excellence Fund
  3. Achievement Rewards for College Scientists Foundation, Inc. (ARCS)
  4. Scientific User Facilities Division, Office of Basic Energy Sciences, U.S. Department of Energy [CNMS2010-233]

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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.; 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., similar to 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.

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