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review article

Chromatin Proteomics to Study Epigenetics - Challenges and Opportunities

van Mierlo, Guido  
•
Vermeulen, Michiel
January 1, 2021
Molecular & Cellular Proteomics

Regulation of gene expression is essential for the functioning of all eukaryotic organisms. Understanding gene expression regulation requires determining which proteins interact with regulatory elements in chromatin. MS-based analysis of chromatin has emerged as a powerful tool to identify proteins associated with gene regulation, as it allows studying protein function and protein complex formation in their in vivo chromatin-bound context. Total chromatin isolated from cells can be directly analyzed using MS or further fractionated into transcriptionally active and inactive chromatin prior to MS-based analysis. Newly formed chromatin that is assembled during DNA replication can also be specifically isolated and analyzed. Furthermore, capturing specific chromatin domains facilitates the identification of previously unknown transcription factors interacting with these domains. Finally, in recent years, advances have been made toward identifying proteins that interact with a single genomic locus of interest. In this review, we highlight the power of chromatin proteomics approaches and how these provide complementary alternatives compared with conventional affinity purification methods. Furthermore, we discuss the biochemical challenges that should be addressed to consolidate and expand the role of chromatin proteomics as a key technology in the context of gene expression regulation and epigenetics research in health and disease.

  • Details
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Type
review article
DOI
10.1074/mcp.R120.002208
Web of Science ID

WOS:000651579500001

Author(s)
van Mierlo, Guido  
Vermeulen, Michiel
Date Issued

2021-01-01

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

Published in
Molecular & Cellular Proteomics
Volume

20

Article Number

100056

Subjects

Biochemical Research Methods

•

Biochemistry & Molecular Biology

•

mass-spectrometry

•

affinity purification

•

transcription factors

•

interacting proteins

•

dna-binding

•

proximity

•

reveals

•

biotinylation

•

complexes

•

regions

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
UPDEPLA  
Available on Infoscience
June 19, 2021
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/178972
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