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Nucleosome Binding Alters the Substrate Bonding Environment of Histone H3 Lysine 36 Methyltransferase NSD2
- 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.
- Subjects :
- Models, Molecular
0301 basic medicine
S-Adenosylmethionine
010402 general chemistry
Methylation
01 natural sciences
Biochemistry
Article
Catalysis
03 medical and health sciences
Histone H3
Colloid and Surface Chemistry
Histone methylation
Humans
Nucleosome
Histone octamer
Nucleosome binding
Binding Sites
Chemistry
Computational Biology
Histone-Lysine N-Methyltransferase
General Chemistry
Models, Theoretical
Linker DNA
Nucleosomes
0104 chemical sciences
Repressor Proteins
030104 developmental biology
Histone methyltransferase
Chromatosome
Biophysics
Protein Binding
Subjects
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