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Portable, Battery Operated Capillary Electrophoresis with Optical Isomer Resolution Integrated with Ionization Source for Mass Spectrometry
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  • 作者:Mehdi Moini…
  • 关键词:Battery operated CE ; Ultrafast CE ; Integrated ionization source ; Optical isomers ; Amino acids
  • 刊名:Journal of The American Society for Mass Spectrometry
  • 出版年:2016
  • 出版时间:March 2016
  • 年:2016
  • 卷:27
  • 期:3
  • 页码:388-393
  • 全文大小:610 KB
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  • 作者单位:Mehdi Moini (1)
    Christopher M. Rollman (1)

    1. Department of Forensic Sciences, George Washington University, Washington, DC, 20007, USA
  • 刊物主题:Analytical Chemistry; Biotechnology; Organic Chemistry; Proteomics; Bioinformatics;
  • 出版者:Springer US
  • ISSN:1879-1123
文摘
We introduce a battery operated capillary electrophoresis electrospray ionization (CE/ESI) source for mass spectrometry with optical isomer separation capability. The source fits in front of low or high resolution mass spectrometers similar to a nanospray source with about the same weight and size. The source has two high voltage power supplies (±25 kV HVPS) capable of operating in forward or reverse polarity modes and powered by a 12 V rechargeable lithium ion battery with operation time of ~10 h. In ultrafast CE mode, in which short narrow capillaries (≤15 μm i.d., 15–25 cm long) and field gradients ≥1000 V/cm are used, peak widths at the base are <1 s wide. Under these conditions, the source provides high resolution separation, including optical isomer resolution in ~1 min. Using a low resolution mass spectrometer (LTQ Velos) with a scan time of 0.07 s/scan, baseline separation of amino acids and their optical isomers were achieved in ~1 min. Moreover, bovine serum albumin (BSA) was analyzed in ~1 min with 56% coverage using the data-dependent MS/MS. Using a high resolution mass spectrometer (Thermo Orbitrap Elite) with 15,000 resolution, the fastest scan time achieved was 0.15 s, which was adequate for CE-MS analysis when optical isomer separation is not required or when the optical isomers were well separated. Figures of merit including a detection limit of 2 fmol and linear dynamic range of two orders of magnitude were achieved for amino acids.

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