| Literature DB >> 26929135 |
Maxence Wisztorski1, Annie Desmons1, Jusal Quanico1, Benoit Fatou1, Jean-Pascal Gimeno1,2, Julien Franck1, Michel Salzet1, Isabelle Fournier1.
Abstract
Tissue microenvironment characterization presents a challenge for a better understanding of the full complexity of a pathology. Unfortunately, making a precise "picture" of the disease needs an efficient microsampling method coupled to an accurate localization for performing region-dependent proteomics. Here, we present a method that enables rapid and reproducible extraction of proteins from a tissue section to analyze a specific region at a millimeter scale. The method used a liquid-microjunction extraction with conventional detergent solution for proteomics analysis. We successfully performed immunoblotting experiments and showed the possibility to retrieve and identify more than 1400 proteins from a 1-mm diameter spot size on tissue sections with a high degree of reproducibility both qualitatively and quantitatively. Moreover, the small size of the extracted region achieved by this sampling method allows the possibility to perform multiple extractions on different tissue section points. Ten points on a sagittal rat brain tissue section were analyzed and the measured proteins clearly distinguished the different parts of the brain, thus permitting precise functional mapping. We thus demonstrate that with this technology, it is possible to map the tissue microenvironment and gain an understanding of the molecular mechanisms at millimeter resolution.Entities:
Keywords: LESA; Protein micro-extraction; Surface sampling; Technology; Tissue microproteomics
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Year: 2016 PMID: 26929135 DOI: 10.1002/pmic.201500508
Source DB: PubMed Journal: Proteomics ISSN: 1615-9853 Impact factor: 3.984