4.6 Article

Impact of sample preparation in peptide/protein profiling in human serum by MALDI-TOF mass spectrometry

Journal

JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
Volume 46, Issue 1, Pages 157-164

Publisher

ELSEVIER
DOI: 10.1016/j.jpba.2007.10.015

Keywords

MALDI-TOF-MS; serum; proteins; biomarkers; breast cancer

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The low molecular weight (LMW) serum proteome (<15 kDa) is the most generally informative from a medical point of view. Different sample pre-treatment approaches and devices for serum depletion in high-abundant proteins were tested in order to analyze, by MALDI-TOF-MS (both in linear and reflectron acquisition mode), the serum low molecular weight proteins/peptides. The best results in terms of detected ions number and abundance were obtained by using ultrafiltration of serum on 30 kDa molecular weight cut off membranes followed by miniaturized reverse-phase solid-phase extraction (mu-SPE) as sample pre-treatment; this procedure yielded also satisfactory within-sample and sample-to-sample repeatability (on both m/z values and peak intensity of the main observable ions). The procedure was finally applied to serum samples of breast cancer patients, and the relevant results compared to normal samples seem to be promising for the individuation of different profiles (linear and reflectron mode) and/or peptides capable of differentiating for malignancies (reflectron mode). (c) 2007 Elsevier B.V. All rights reserved.

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