In-depth quantitative profiling of human plasma samples for biomarker discovery remains quite challenging. One promising alternative to chemical derivatization with stable isotope labels for quantitative comparisons is direct, label-free, quantitative comparison of raw LC–MS data. But, in order to achieve high-sensitivity detection of low-abundance proteins, plasma proteins must be extensively pre-fractionated, and results from LC–MS runs of all fractions must be integrated efficiently in order to avoid misidentification of variations in fractionation from sample to sample as “apparent” biomarkers. This protocol describes a powerful 3D protein profiling method for comprehensive analysis of human serum or plasma proteomes, which combines abundant protein depletion and high-sensitivity GeLC–MS/MS with label-free quantitation of candidate biomarkers.
CITATION STYLE
Beer, L. A., Tang, H. Y., Barnhart, K. T., & Speicher, D. W. (2011). Plasma Biomarker Discovery Using 3D Protein Profiling Coupled with Label-Free Quantitation. In Methods in Molecular Biology (Vol. 728, pp. 3–27). Humana Press Inc. https://doi.org/10.1007/978-1-61779-068-3_1
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