Abstract

In recent years, capillary electrophoresis coupled to mass spectrometry (CE-MS) has been increasingly applied in clinical research especially in the context of chronic and age-associated diseases, such as chronic kidney disease, heart failure and cancer. Biomarkers identified using this technique are already used for diagnosis, prognosis and monitoring of these complex diseases, as well as patient stratification in clinical trials. CE-MS allows for a comprehensive assessment of small molecular weight proteins and peptides (<20 kDa) through the combination of the high resolution and reproducibility of CE and the distinct sensitivity of MS, in a high-throughput system. In this study we assessed CE-MS analytical performance with regards to its inter- and intra-day reproducibility, variability and efficiency in peptide detection, along with a characterization of the urinary peptidome content. To this end, CE-MS performance was evaluated based on 72 measurements of a standard urine sample (60 for inter- and 12 for intra-day assessment) analyzed during the second quarter of 2021. Analysis was performed per run, per peptide, as well as at the level of biomarker panels. The obtained datasets showed high correlation between the different runs, low variation of the ten highest average individual log2 signal intensities (coefficient of variation, CV < 10%) and very low variation of biomarker panels applied (CV close to 1%). The findings of the study support the analytical performance of CE-MS, underlining its value for clinical application.

Highlights

  • Capillary electrophoresis coupled to mass spectrometry (CE-MS) is a proteomic platform that has been extensively employed as a tool for clinical application, mainly for the non-invasive assessment of biomarkers in urine [1,2,3]

  • The descriptive statistics based on the log2 signal intensities of the detected peptides were calculated for each run (Supplementary Table S1)

  • The CE-MS presents a robust and reproducible platform for peptide analysis to be applied in clinical proteomics

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Summary

Introduction

Capillary electrophoresis coupled to mass spectrometry (CE-MS) is a proteomic platform that has been extensively employed as a tool for clinical application, mainly for the non-invasive assessment of biomarkers in urine [1,2,3]. The approach relies on several steps leading to the biomarker identification and biomarker model construction. Before this can happen there are several quality control stages to ensure successful completion of each analysis, as described in detail in numerous review articles [1,3,4] and summarized below. Separation is performed based on analyte electrophoretic mobility, determined by its charge and size. Since analytes may interact with silanol groups in the wall of the capillaries, interfering with separation, different capillary coating approaches were investigated to prevent this interaction [6]

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