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Methods Enzymol. 2016;573:241-59. doi: 10.1016/bs.mie.2016.02.001. Epub 2016 Mar 4.

Expression, Purification, and Biochemical Analysis of the LSD1/KDM1A Histone Demethylase.

Author information

1
Boston Children's Hospital, Boston, MA, United States; Harvard Medical School, Boston, MA, United States.
2
Boston Children's Hospital, Boston, MA, United States; Harvard Medical School, Boston, MA, United States. Electronic address: yang_shi@hms.harvard.edu.

Abstract

Posttranslational modifications (PTMs) of histones play important roles in the regulation of chromatin architecture and gene transcription. A decade ago, it was still believed that methyl groups could not be removed from histones, until the first histone demethylase LSD1 (lysine-specific demethylase 1; also known as KDM1A) was identified. This discovery initiated an era in the understanding of chromatin dynamic regulation by active histone demethylation. Since then, the repertoire of histone demethylases has expanded, and our understanding of the molecular mechanisms, structures, and macromolecular complexes of the demethylases has grown significantly. Histone demethylases have emerged as important players in developmental processes and have been linked to human diseases and cancer. Studies highlighting the functions of LSD1 have significantly increased our understanding of chromatin biology and have revealed that new facets of histone demethylases remain to be discovered. In vitro methods have been developed to assess the biochemistry, structure, and enzymology of lysine demethylases. Here, we describe the methods of expression, purification, and biochemical analysis that we have successfully used in characterizing the functions of LSD1.

KEYWORDS:

Chromatin; Demethylase; Epigenetics; Histones; LSD1; Methylation

PMID:
27372756
DOI:
10.1016/bs.mie.2016.02.001
[Indexed for MEDLINE]

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