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Nucleosome Binding Alters the Substrate Bonding Environment of Histone H3 Lysine 36 Methyltransferase NSD2

Authors :
Patrick McDevitt
Rosalie Matico
Vern L. Schramm
Wangfang Hou
Myles B. Poulin
Marc A. Holbert
Jessica L. Schneck
Source :
Journal of the American Chemical Society. 138:6699-6702
Publication Year :
2016
Publisher :
American Chemical Society (ACS), 2016.

Abstract

Nuclear receptor-binding SET domain protein 2 (NSD2) is a histone H3 lysine 36 (H3K36)-specific methyltransferase enzyme that is overexpressed in a number of cancers, including multiple myeloma. NSD2 binds to S-adenosyl-L-methionine (SAM) and nucleosome substrates to catalyze the transfer of a methyl group from SAM to the ε-amino group of histone H3K36. Equilibrium binding isotope effects and density functional theory calculations indicate that the SAM methyl group is sterically constrained in complex with NSD2, and that this steric constraint is released upon nucleosome binding. Together, these results show that nucleosome binding to NSD2 induces a significant change in the chemical environment of enzyme-bound SAM.

Details

ISSN :
15205126 and 00027863
Volume :
138
Database :
OpenAIRE
Journal :
Journal of the American Chemical Society
Accession number :
edsair.doi.dedup.....6f6f08fa37b87ae8262d78128ed8560b
Full Text :
https://doi.org/10.1021/jacs.6b01612