A fully automated FAIMS-DIA mass spectrometry-based proteomic pipeline

Cell Rep Methods. 2023 Oct 23;3(10):100593. doi: 10.1016/j.crmeth.2023.100593. Epub 2023 Sep 19.

Abstract

Here, we present a standardized, "off-the-shelf" proteomics pipeline working in a single 96-well plate to achieve deep coverage of cellular proteomes with high throughput and scalability. This integrated pipeline streamlines a fully automated sample preparation platform, a data-independent acquisition (DIA) coupled with high-field asymmetric waveform ion mobility spectrometer (FAIMS) interface, and an optimized library-free DIA database search strategy. Our systematic evaluation of FAIMS-DIA showing single compensation voltage (CV) at -35 V not only yields the deepest proteome coverage but also best correlates with DIA without FAIMS. Our in-depth comparison of direct-DIA database search engines shows that Spectronaut outperforms others, providing the highest quantifiable proteins. Next, we apply three common DIA strategies in characterizing human induced pluripotent stem cell (iPSC)-derived neurons and show single-shot mass spectrometry (MS) using single-CV (-35 V)-FAIMS-DIA results in >9,000 quantifiable proteins with <10% missing values, as well as superior reproducibility and accuracy compared with other existing DIA methods.

Keywords: CP: Biotechnology; CP: Systems biology; DDA; DIA; FAIMS; automation; database search; mass spectrometry; proteomics; single-shot MS.

MeSH terms

  • Humans
  • Induced Pluripotent Stem Cells* / chemistry
  • Proteome / analysis
  • Proteomics* / methods
  • Reproducibility of Results
  • Tandem Mass Spectrometry / methods

Substances

  • Proteome