Phosphopeptide enrichment by aliphatic hydroxy acid-modified metal oxide chromatography for nano-LC-MS/MS in proteomics applications

Mol Cell Proteomics. 2007 Jun;6(6):1103-9. doi: 10.1074/mcp.T600060-MCP200. Epub 2007 Feb 23.

Abstract

We developed novel methods for phosphopeptide enrichment using aliphatic hydroxy acid-modified metal oxide chromatography (MOC). Titania and zirconia were successfully applied to enrich phosphopeptides with the aid of aliphatic hydroxy acids, such as lactic acid and beta-hydroxypropanoic acid, to reduce the interaction between acidic non-phosphopeptides and the metal oxides. These methods removed the vast majority of non-phosphopeptides from phosphoprotein standard digests, and large numbers of phosphopeptides could be readily identified. The methods were coupled with nano-LC-MS/MS systems without difficulty. Recovery of phosphopeptides in MOC varied greatly from peptide to peptide, ranging from a few percent to 100%, and the average was almost 50%. Repeatability and linearity were satisfactory. In an examination of the cytoplasmic fraction of HeLa cells, more than 1000 phosphopeptides were identified using lactic acid-modified titania MOC and beta-hydroxypropanoic acid-modified zirconia MOC, respectively. The overlap between phosphopeptides enriched by these two methods was 40%, and the combined results provided 1646 unique phosphopeptides. To our knowledge, this is the first successful application of a single MOC-based approach to phosphopeptide enrichment from complex biological samples such as cell lysates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Cell Extracts / chemistry
  • Chromatography, Liquid
  • Cytoplasm / chemistry
  • Cytoplasm / drug effects
  • HeLa Cells
  • Humans
  • Hydroxy Acids / chemistry*
  • Hydroxy Acids / pharmacology
  • Mass Spectrometry
  • Molecular Sequence Data
  • Nanotechnology*
  • Phosphopeptides / analysis
  • Phosphopeptides / chemistry
  • Phosphopeptides / isolation & purification*
  • Proteomics / instrumentation*
  • Proteomics / methods*
  • Reproducibility of Results

Substances

  • Cell Extracts
  • Hydroxy Acids
  • Phosphopeptides