Urinary proteome analysis using capillary electrophoresis coupled to mass spectrometry: A powerful tool in clinical diagnosis, prognosis and therapy evaluation

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Abstract

Proteome analysis has emerged as a powerful tool to decipher (patho) physiological processes, resulting in the establishment of the field of clinical proteomics. One of the main goals is to discover biomarkers for diseases from tissues and body fluids. Due to the enormous complexity of the proteome, a separation step is required for mass spectrometry (MS)-based proteome analysis. In this review, the advantages and limitations of protein separation by two-dimensional gel electrophoresis, liquid chromatography, surface-enhanced laser desorption/ionization and capillary electrophoresis (CE) for proteomic analysis are described, focusing on CE-MS. CE-MS enables separation and detection of the small molecular weight proteome in biological fluids with high reproducibility and accuracy in one single processing step and in a short time. As sensitive and specific single biomarkers generally may not exist, a strategy to overcome this diagnostic void is shifting from single analyte detection to simultaneous analysis of multiple analytes that together form a disease-specific pattern. Such approaches, however, are accompanied with additional challenges, which we will outline in this review. Besides the choice of adequate technological platforms, a high level of standardization of proteomic measurements and data processing is also necessary to establish proteomic profiling. In this regard, demands concerning study design, choice of specimens, sample preparation, proteomic data mining, and clinical evaluation should be considered before performing a proteomic study.

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Mischak, H., Schiffer, E., Zürbig, P., Dakna, M., & Metzger, J. (2009, October 1). Urinary proteome analysis using capillary electrophoresis coupled to mass spectrometry: A powerful tool in clinical diagnosis, prognosis and therapy evaluation. Journal of Medical Biochemistry. https://doi.org/10.2478/v10011-009-0020-0

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