Online Microreactor Titanium Dioxide RPLC-LTQ-Orbitrap MS Automated Platform for Shotgun Analysis of (Phospho) Proteins in Human Amniotic Fluid

被引:1
作者
Temporini, Caterina [1 ]
Nicoli, Raul [2 ]
Tiengo, Alessandra [3 ]
Barbarini, Nicola [3 ]
Calleri, Enrica [1 ]
Galliano, Monica [4 ]
Magni, Paolo [3 ]
Rudaz, Serge [2 ]
Veuthey, Jean-Luc [2 ]
Regazzoni, Luca [5 ]
Aldini, Giancarlo [5 ]
Massolini, Gabriella [1 ]
机构
[1] Univ Pavia, Dept Drug Sci, I-27100 Pavia, Italy
[2] Univ Lausanne, Univ Geneva, Sch Pharmaceut Sci, Lab Analyt Pharmaceut Chem, Geneva, Switzerland
[3] Univ Pavia, Dept Comp Engn & Syst Sci Pavia, I-27100 Pavia, Italy
[4] Univ Pavia, Dept Biochem, I-27100 Pavia, Italy
[5] Univ Milan, Dept Pharmaceut Sci Pietro Pratesi, I-20133 Milan, Italy
关键词
Phosphoproteins; TiO2; Online; digestion and LC-MS-MS; Human amniotic fluid; IGFBP-1; Osteopontin; MASS-SPECTROMETRY; PROTEOMIC ANALYSIS; PHOSPHORYLATION SITES; QUANTITATIVE-ANALYSIS; PHOSPHOPROTEOME ANALYSIS; ANALYTICAL STRATEGIES; IDENTIFICATION; PHOSPHOPEPTIDES; CHROMATOGRAPHY; OSTEOPONTIN;
D O I
10.1007/s10337-013-2567-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Biomarkers in amniotic fluid (AF) include both non-modified and phosphorylated proteins and can be used in the diagnosis of pregnancy-associated pathologic conditions. In this work, an integrated LC-MS method for selective, sensitive and reproducible analysis of phosphorylation in proteins has been applied to AF. Online digestion of (phospho) proteins was coupled with the selective enrichment on a TiO2 trap, and separated by RPLC-MSn of both normal and phosphorylated produced peptides. First, an AF-pooled sample was analyzed and a general map of contained proteins and biomarkers was derived in a single run. Then, individual AF samples were analyzed with a downscaled platform with improved sensitivity. On purpose, a trypsin-based CIMA (R) minidisk was used for online digestion of AF. The obtained protein profile was highly consistent with the one obtained with traditional off-line digestions. Moreover, the use of a specific phospho-enrichment tool followed by LTQ-Orbitrap, enhanced the confidence in the determination of protein phosphorylation state and phosphorylation sites. The phosphorylation sites of IGFBP-1 and osteopontin present in the AF of two individual samples were monitored with a total of 24 and 17 phosphopeptides, respectively, encoding for 12 putative novel phosphorylation sites in addition to known sites.
引用
收藏
页码:39 / 50
页数:12
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