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

被引:38
作者
Aresta, Antonella [1 ]
Calvano, Cosima D. [1 ]
Palmisano, Francesco [1 ]
Zambonin, Carlo G. [1 ]
Monaco, Alessandro [2 ]
Tornmasi, Stefania [2 ]
Pilato, Brunella [2 ]
Paradiso, Angelo [2 ]
机构
[1] Univ Bari, Dipartmento Chim, Ctr Interdipartimentale Ric SMART, I-70126 Bari, Italy
[2] Ist Nazl Giovanni Paolo 2, I-70126 Bari, Italy
关键词
MALDI-TOF-MS; serum; proteins; biomarkers; breast cancer;
D O I
10.1016/j.jpba.2007.10.015
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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.
引用
收藏
页码:157 / 164
页数:8
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