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Proteomic characterization of pediatric craniopharyngioma intracystic fluid by LC ‐ MS top‐down/bottom‐up integrated approaches
Author(s) -
Martelli Claudia,
Iavarone Federica,
Vincenzoni Federica,
Rossetti Diana Valeria,
D'Angelo Luca,
Tamburrini Gianpiero,
Caldarelli Massimo,
Di Rocco Concezio,
Messana Irene,
Castagnola Massimo,
Desiderio Claudia
Publication year - 2014
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/elps.201300578
Subject(s) - chemistry , apolipoprotein b , glycoprotein , proteomics , proteome , trypsin , biochemistry , craniopharyngioma , cholesterol , biology , gene , enzyme , endocrinology
The combination of top‐down and bottom‐up platforms was utilized for the LC ‐ MS proteomic characterization of the intracystic fluid of adamantinomatous craniopharyngioma pediatric brain tumor disease. Proteins and peptides characterization was achieved by high‐resolution LC ‐ ESI ‐ LTQ ‐ O rbitrap‐ MS analysis while low‐resolution LC ‐ ESI ‐ IT ‐ MS was applied for the complete screening of the samples and the evaluation of the protein distribution within patients. Top‐down analyses were applied to liquid/liquid extracted samples while bottom‐up analyses were performed after trypsin digestion of both untreated and pretreated samples. The two proteomic approaches were complementary for the characterization of the proteome of craniopharyngioma intracystic fluid. Proteins and peptides involved in inflammation, mineralization processes and lipid transport were identified, in agreement with the calcium flecks, cholesterol granules and bone residues characteristic of this fluid. Apolipoprotein A ‐I, A‐II, C ‐I and J , hemoglobin fragments, ubiquitin, α‐2‐ HS ‐glycoprotein or fetuin A, α‐1‐antichymotrypsin, vitamin D binding protein, and α‐1‐acid glycoprotein were characterized. These data could be relevant for the comprehension of the processes involved in the pathogenesis of the disease and the development of the cyst and could contribute to the individuation of therapeutic targets for the reduction of the cyst volume delaying and/or avoiding invasive surgical treatments.

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