Versatile, sensitive liquid chromatography mass spectrometry - Implementation of 10 μm OT columns suitable for small molecules, peptides and proteins

Sci Rep. 2016 Nov 29:6:37507. doi: 10.1038/srep37507.

Abstract

We have designed a versatile and sensitive liquid chromatographic (LC) system, featuring a monolithic trap column and a very narrow (10 μm ID) fused silica open tubular liquid chromatography (OTLC) separation column functionalized with C18-groups, for separating a wide range of molecules (from small metabolites to intact proteins). Compared to today's capillary/nanoLC approaches, our system provides significantly enhanced sensitivity (up to several orders) with matching or improved separation efficiency, and highly repeatable chromatographic performance. The chemical properties of the trap column and the analytical column were fine-tuned to obtain practical sample loading capacities (above 2 μg), an earlier bottleneck of OTLC. Using the OTLC system (combined with Orbitrap mass spectrometry), we could perform targeted metabolomics of sub-μg amounts of exosomes with 25 attogram detection limit of a breast cancer-related hydroxylated cholesterol. With the same set-up, sensitive bottom-up proteomics (targeted and untargeted) was possible, and high-resolving intact protein analysis. In contrast to state-of-the-art packed columns, our platform performs chromatography with very little dilution and is "fit-for-all", well suited for comprehensive analysis of limited samples, and has potential as a tool for challenges in diagnostics.

MeSH terms

  • Animals
  • Axin Protein / isolation & purification
  • Breast Neoplasms / chemistry
  • Breast Neoplasms / diagnosis*
  • Breast Neoplasms / metabolism
  • Chromatography, Liquid / instrumentation*
  • Chromatography, Liquid / methods
  • Exosomes / chemistry
  • Female
  • Humans
  • Hydroxycholesterols / isolation & purification*
  • Mice
  • Peptides / isolation & purification*
  • Proteomics / instrumentation*
  • Proteomics / methods
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Tandem Mass Spectrometry / instrumentation*
  • Tandem Mass Spectrometry / methods

Substances

  • Axin Protein
  • Axin1 protein, mouse
  • Hydroxycholesterols
  • Peptides