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Quantification of run order effect on chromatography : mass spectrometry profiling data

Surowiec, Izabella (author)
Umeå universitet,Kemiska institutionen
Johansson, Erik (author)
Stenlund, Hans (author)
Swedish Metabolomics Centre, Umeå, Sweden
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Rantapää-Dahlqvist, Solbritt (author)
Umeå universitet,Reumatologi
Bergström, Sven, 1973- (author)
Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten),Institutionen för klinisk mikrobiologi
Normark, Johan (author)
Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten),Institutionen för klinisk mikrobiologi,Johan Normark
Trygg, Johan (author)
Umeå universitet,Kemiska institutionen,Sartorius Stedim Data Analytics, Umeå, Sweden
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 (creator_code:org_t)
Elsevier BV, 2018
2018
English.
In: Journal of Chromatography A. - : Elsevier BV. - 0021-9673 .- 1873-3778. ; 1568, s. 229-234
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Chromatographic systems coupled with mass spectrometry detection are widely used in biological studies investigating how levels of biomolecules respond to different internal and external stimuli. Such changes are normally expected to be of low magnitude and therefore all experimental factors that can influence the analysis need to be understood and minimized. Run order effect is commonly observed and constitutes a major challenge in chromatography-mass spectrometry based profiling studies that needs to be addressed before the biological evaluation of measured data is made. So far there is no established consensus, metric or method that quickly estimates the size of this effect. In this paper we demonstrate how orthogonal projections to latent structures (OPLS®) can be used for objective quantification of the run order effect in profiling studies. The quantification metric is expressed as the amount of variation in the experimental data that is correlated to the run order. One of the primary advantages with this approach is that it provides a fast way of quantifying run-order effect for all detected features, not only internal standards. Results obtained from quantification of run order effect as provided by the OPLS can be used in the evaluation of data normalization, support the optimization of analytical protocols and identification of compounds highly influenced by instrumental drift. The application of OPLS for quantification of run order is demonstrated on experimental data from plasma profiling performed on three analytical platforms: GCMS metabolomics, LCMS metabolomics and LCMS lipidomics.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Reumatologi och inflammation (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Rheumatology and Autoimmunity (hsv//eng)

Keyword

Run order effect quantification
Mass spectrometry profiling
OPLS
Instrumental drift

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