Brain Region-Specific Dynamics of On-Tissue Protein Digestion Using MALDI Mass Spectrometry Imaging

被引:21
作者
Heijs, Bram [1 ]
Tolner, Else A. [2 ,3 ]
Bovee, Judith V. M. G. [4 ]
van den Maagdenberg, Am M. J. M. [2 ,3 ]
McDonnell, Liam A. [1 ,4 ,5 ]
机构
[1] Leiden Univ, Med Ctr, Ctr Prote & Metab, NL-2333 ZA Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Neurol, NL-2333 ZA Leiden, Netherlands
[3] Leiden Univ, Med Ctr, Dept Human Genet, NL-2333 ZA Leiden, Netherlands
[4] Leiden Univ, Med Ctr, Dept Pathol, NL-2333 ZA Leiden, Netherlands
[5] Fdn Pisana Sci ONLUS, I-56125 Pisa, Italy
关键词
on-tissue digestion; MALDI mass spectrometry imaging; proteolysis; PARAFFIN-EMBEDDED TISSUE; QUANTIFICATION; NORMALIZATION; QUANTITATION;
D O I
10.1021/acs.jproteome.5b00849
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In mass spectrometry imaging (MSI), on-tissue proteolytic digestion is performed to access larger protein pecies and to assign protein identities through matching the detected peaks with those obtained by LC MS/MS analyses of tissue extracts. The on tissue proteolytic digestion also allows the analysis of proteins from formalin-fixed, paraffin-embedded tissues. For these reasons, on-tissue digestion-based MSI is frequently used in clinical investigations, for example, to determine changes in protein content and distribution associated with a disease. In this work, we sought to investigate the completeness and uniformity of the digestion in on-tissue digestion MSI. On the basis of an extensive experiment investigating three groups with varying incubation times: (i) 1.5 h, (ii) 3 h, and (iii) 18 h, we have found that longer incubation times improve the repeatability of the analyses. Furthermore, we discovered morphology-associated differences in the completeness of the proteolysis for short incubation the notion that a more complete proteolysis allows better quantitation.
引用
收藏
页码:5348 / 5354
页数:7
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