Optimization of MALDI-TOF mass spectrometry imaging for the visualization and comparison of peptide distributions in dry-cured ham muscle fibers

被引:32
作者
Maslov, Dina Resetar [1 ,2 ]
Svirkova, Anastasiya [2 ]
Allmaier, Gunter [2 ]
Marchetti-Deschamann, Martina [2 ]
Pavelic, Sandra Kraljevic [1 ]
机构
[1] Univ Rijeka, Dept Biotechnol, Ctr High Throughput Technol, Radmile Matejcic 2, Rijeka 51000, Croatia
[2] TU Wien, Inst Chem Technol & Analyt, Getreidemarkt 9-164, A-1060 Vienna, Austria
关键词
MALDI mass spectrometry imaging; Sample preparation optimization; Dry-cured ham; Spatially resolved peptides; PROTEOMIC IDENTIFICATION; MYOFIBRILLAR PROTEINS; SAMPLE PREPARATION; QUALITY MEASURES; TISSUE-SECTIONS; SKELETAL-MUSCLE; PARMA; MEAT; NEUROPEPTIDES; OLIGOPEPTIDES;
D O I
10.1016/j.foodchem.2018.12.126
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In this article, a matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI MSI)-based study was designed in order to selectively map and compare the peptides present in slices of Biceps femoris, Istrian dry-cured ham muscles, from the same production batch. A systematic sample preparation process was optimized, which comprises embedding samples of Biceps femoris, cryo-sectioning, glass slide mounting, a nine-step washing protocol, MALDI matrix sublimation and recrystallization. This process efficiently preserved sample morphology and removed the high salt and lipid content, which was present in the samples as a result of the dry-curing production process. We show that MALDI MSI, in combination with principal component analysis, can be used to monitor subtle changes in proteolysis outcome within the same dry-cured ham muscle type, resulting from differentially resolved spatial data. The peptides identified in Istrian dry-cured ham may therefore be studied further, as putative biomarkers for this specific product.
引用
收藏
页码:275 / 286
页数:12
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