4.8 Article

Picoflow Liquid Chromatography-Mass Spectrometry for Ultrasensitive Bottom-Up Proteomics Using 2-mu m-i.d. Open Tubular Columns

Journal

ANALYTICAL CHEMISTRY
Volume 92, Issue 7, Pages 4711-4715

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.9b05639

Keywords

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Funding

  1. National Science Foundation [CHE1904645]
  2. Oklahoma Center for the Advancement of Science and Technology [HR17-022]
  3. Laboratory Directed Research and Development award from Pacific Northwest National Laboratory (PNNL)
  4. NIGMS [P41 GM103493]
  5. Office of Biological and Environmental Research

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In many areas of application, key objectives of chemical separation and analysis are to minimize the sample quantity while maximizing the chemical information obtained. Increasing measurement sensitivity is especially critical for proteomics research, especially when processing trace samples and where multiple measurements are desired. A rich collection of technologies has been developed, but the resulting sensitivity remains insufficient for achieving in-depth coverage of proteomic samples as small as single cells. Here, we combine picoliter-scale liquid chromatography (picoLC) with mass spectrometry (MS) to address this issue. The picoLC employs a 2-mu m-i.d. open tubular column to reduce the sample input needed to greatly increase the sensitivity achieved using electrospray ionization (ESI) with MS. With this picoLC-MS system, we show that we can identify similar to 1000 proteins reliably using only 75 pg of tryptic peptides, representing a 10-100-fold sensitivity improvement compared with the state-of-the-art liquid chromatography (LC) or capillary electrophoresis (CE)-MS methods. PicoLC-MS extends the limit of separation science and is expected to be a powerful tool for single cell proteomics.

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