Abstract

BackgroundProteomic matrix-assisted laser desorption/ionisation (MALDI) linear time-of-flight (TOF) mass spectrometry (MS) may be used to produce protein profiles from biological samples with the aim of discovering biomarkers for disease. However, the raw protein profiles suffer from several sources of bias or systematic variation which need to be removed via pre-processing before meaningful downstream analysis of the data can be undertaken. Baseline subtraction, an early pre-processing step that removes the non-peptide signal from the spectra, is complicated by the following: (i) each spectrum has, on average, wider peaks for peptides with higher mass-to-charge ratios (m/z), and (ii) the time-consuming and error-prone trial-and-error process for optimising the baseline subtraction input arguments. With reference to the aforementioned complications, we present an automated pipeline that includes (i) a novel ‘continuous’ line segment algorithm that efficiently operates over data with a transformed m/z-axis to remove the relationship between peptide mass and peak width, and (ii) an input-free algorithm to estimate peak widths on the transformed m/z scale.ResultsThe automated baseline subtraction method was deployed on six publicly available proteomic MS datasets using six different m/z-axis transformations. Optimality of the automated baseline subtraction pipeline was assessed quantitatively using the mean absolute scaled error (MASE) when compared to a gold-standard baseline subtracted signal. Several of the transformations investigated were able to reduce, if not entirely remove, the peak width and peak location relationship resulting in near-optimal baseline subtraction using the automated pipeline. The proposed novel ‘continuous’ line segment algorithm is shown to far outperform naive sliding window algorithms with regard to the computational time required. The improvement in computational time was at least four-fold on real MALDI TOF-MS data and at least an order of magnitude on many simulated datasets.ConclusionsThe advantages of the proposed pipeline include informed and data specific input arguments for baseline subtraction methods, the avoidance of time-intensive and subjective piecewise baseline subtraction, and the ability to automate baseline subtraction completely. Moreover, individual steps can be adopted as stand-alone routines.Electronic supplementary materialThe online version of this article (doi:10.1186/s12953-016-0107-8) contains supplementary material, which is available to authorized users.

Highlights

  • Proteomic matrix-assisted laser desorption/ionisation (MALDI) linear time-of-flight (TOF) mass spectrometry (MS) may be used to produce protein profiles from biological samples with the aim of discovering biomarkers for disease

  • Matrixassisted laser desorption/ionisation (MALDI) linear timeof-flight (TOF) mass spectrometry (MS) is a widely used technology for biomarker discovery as it can create a representative profile of polypeptide expression from biological samples

  • The present paper focuses on optimising methods for the baseline subtraction step of preprocessing of the raw spectra

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Summary

Introduction

Proteomic matrix-assisted laser desorption/ionisation (MALDI) linear time-of-flight (TOF) mass spectrometry (MS) may be used to produce protein profiles from biological samples with the aim of discovering biomarkers for disease. Matrixassisted laser desorption/ionisation (MALDI) linear timeof-flight (TOF) mass spectrometry (MS) is a widely used technology for biomarker discovery as it can create a representative profile of polypeptide expression from biological samples. These profiles are displayed as points of polypeptide abundance (intensity; the y-axis) for a range of mass-to-charge values (m/z; the x-axis). Numerous biomarkers using MALDI TOF-MS have been identified to date [3, 4]

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