Quality Control of nano-LC-MS Systems Using Stable Isotope-Coded Peptides

Proteomics. 2011 Mar;11(6):1049-57. doi: 10.1002/pmic.201000604. Epub 2011 Feb 16.


In analytical sciences, there is a general need for quality control to assess whether a product or a process meets defined requirements. Especially in proteomics, which implies analysis of ten thousands of analytes within a complex mixture, quality control to validate LC-MS performance and method setup is inevitable to achieve day-to-day-, inter-system-, as well as inter-user reproducibility. Thus, results deriving from LC-MS analyses can be benchmarked and the need for system maintenance can be revealed. In particular with the advent of label-free quantification of peptides and proteins, which above all depends on highly stable and reproducible LC separations, HPLC performance has to be appropriately monitored throughout the entire analytical procedure to assure quality and validity of the obtained data. Oftentimes, proteolytic digests of standard proteins are used in this context; however, this approach implies some limitations, such as inadequate batch-to-batch reproducibility, limited (if any) dynamic range and compositional inflexibility. Here, we present an alternative strategy of nano-LC-MS/MS quality control based on a mixture of synthetic peptides covering the entire LC-gradient as well as a dynamic range of more than two orders of magnitude. Thus, (i) reproducibility of LC separation, (ii) MS performance (including limit of detection, identification and quantification), as well as (iii) overall nano-LC-MS system performance and reproducibility can be routinely monitored even in highly complex samples.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Blood Platelets / chemistry
  • Blood Proteins / isolation & purification
  • Chromatography, Liquid / standards
  • Data Interpretation, Statistical
  • Humans
  • Isotopes
  • Mitochondrial Proteins / isolation & purification
  • Nanotechnology
  • Peptides / chemistry
  • Peptides / standards*
  • Proteomics / methods
  • Proteomics / standards*
  • Proteomics / statistics & numerical data
  • Quality Control
  • Reference Standards
  • Saccharomyces cerevisiae Proteins / isolation & purification
  • Tandem Mass Spectrometry / methods
  • Tandem Mass Spectrometry / standards*


  • Blood Proteins
  • Isotopes
  • Mitochondrial Proteins
  • Peptides
  • Saccharomyces cerevisiae Proteins