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Lahiri, S.* ; Sun, N. ; Solis-Mezarino, V.* ; Fedisch, A.* ; Ninkovic, J. ; Feuchtinger, A. ; Götz, M. ; Walch, A.K. ; Imhof, A.*

In situ detection of histone variants and modifications in mouse brain using imaging mass spectrometry.

Proteomics 16, 437-447 (2016)
Postprint DOI PMC
Open Access Green
Histone posttranslational modifications and histone variants control the epigenetic regulation of gene expression and affect a wide variety of biological processes. A complex pattern of such modifications and variants defines the identity of cells within complex organ systems and can therefore be used to characterize cells at a molecular level. However, their detection and identification in situ has been limited so far due to lack of specificity, selectivity and availability of anti-histone antibodies. Here, we describe a novel MALDI imaging mass spectrometry (MALDI-IMS) based workflow, which enables us to detect and characterize histones by their intact mass and their correlation with cytological properties of the tissue using novel statistical and image analysis tools. The workflow allows us to characterize the in situ distribution of the major histone variants and their modification in the mouse brain. This new analysis tool is particularly useful for the investigation of expression patterns of the linker histone H1 variants for which suitable antibodies are so far not available.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Hierarchical Clustering Analysis ; Histone Modifications ; Maldi Imaging Mass Spectrometry ; Nuclear Density ; Principal Component Analysis; Epigenetic Mechanisms; Nucleosome Core; H1; Tissue; H4; Reveals; Perspectives; Acetylation; Antibodies; Signatures
Sprache englisch
Veröffentlichungsjahr 2016
Prepublished im Jahr 2015
HGF-Berichtsjahr 2015
ISSN (print) / ISBN 1615-9853
e-ISSN 1615-9861
Zeitschrift Proteomics
Quellenangaben Band: 16, Heft: 3, Seiten: 437-447 Artikelnummer: , Supplement: ,
Verlag Wiley
Verlagsort Hoboken
Begutachtungsstatus Peer reviewed
POF Topic(s) 30205 - Bioengineering and Digital Health
30204 - Cell Programming and Repair
30504 - Mechanisms of Genetic and Environmental Influences on Health and Disease
Forschungsfeld(er) Enabling and Novel Technologies
Stem Cell and Neuroscience
PSP-Element(e) G-500390-001
G-500800-001
G-500300-001
Scopus ID 84958050008
Scopus ID 84955584977
PubMed ID 26593131
Erfassungsdatum 2015-12-02