4.8 Article

A Customizable Flow Injection System for Automated, High Throughput, and Time Sensitive Ion Mobility Spectrometry and Mass Spectrometry Measurements

Journal

ANALYTICAL CHEMISTRY
Volume 90, Issue 1, Pages 737-744

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.7b02986

Keywords

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Funding

  1. National Institute of Environmental Health Sciences of the NIH [R01 ES022190]
  2. National Institute of General Medical Sciences [P41 GM103493]
  3. NIH [P42 ES027704]
  4. Laboratory Directed Research and Development Program at Pacific Northwest National Laboratory
  5. U.S. Department of Energy Office of Biological and Environmental Research Genome Sciences Program
  6. DOE [DE-AC05-76RL0 1830]

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To better understand disease conditions and environmental perturbations, multiomic studies combining proteomic, lipidomic, and metabolomic analyses are vastly increasing in popularity. In a multiomic study, a single sample is typically extracted in multiple ways, and various analyses are performed using different instruments, most often based upon mass spectrometry (MS). Thus, one sample becomes many measurements, making high throughput and reproducible evaluations a necessity. One way to Address the numerous samples and varying instrumental conditions is to utilize a flow injection analysis (FIA) system for rapid, sample injections. While some FIA systems have been created to address these challenges, many have limitations such as costly consumables, low pressure capabilities, limited pressure monitoring, and fixed flow rates. To address these limitations, we created an automated, customizable FIA system capable of operating at a range of flow rates (similar to 50 nL/min to 500 mu L/min) to accommodate both low- and high-flow MS ionization sources. This system also functions at varying analytical throughputs from 24 to 1200 samples per day to enable different MS analysis approaches. Applications ranging from native protein analyses to molecular library construction were performed using the FIA system, and results showed a highly robust and reproducible platform capable of providing consistent performance over many days without carryover, as long as washing buffers specific to each molecular analysis were utilized.

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