Unknown

Dataset Information

0

Photoreactive "nanorulers" detect a novel conformation of full length HDAC3-SMRT complex in solution.


ABSTRACT: Histone deacetylase 3 (HDAC3) is a promising epigenetic drug target for multiple therapeutic applications. Direct interaction between the Deacetylase Activating Domain of the silencing mediator for retinoid or thyroid-hormone receptors (SMRT-DAD) is required for activation of enzymatic activity of HDAC3. The structure of this complex and the nature of interactions with HDAC inhibitors in solution are unknown. Using novel photoreactive HDAC probes, "nanorulers", we determined the distance between the catalytic site of the full-length HDAC3 and SMRT-DAD in solution at physiologically relevant conditions and found it to be substantially different from that predicted by the X-ray model with a ?379-428 aa truncated HDAC3. Further experiments indicated that in solution this distance might change in response to chemical stimuli, while the enzymatic activity remained unaffected. These observations were further validated by Saturation Transfer Difference (STD) NMR experiments. We propose that the observed changes in the distance are an important part of the histone code that remains to be explored. Mapping direct interactions and distances between macromolecules with such "nanorulers" as a function of cellular events facilitates better understanding of basic biology and ways for its manipulation in a cell- and tissue-specific manner.

SUBMITTER: Abdelkarim H 

PROVIDER: S-EPMC3880688 | biostudies-literature | 2013 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

Photoreactive "nanorulers" detect a novel conformation of full length HDAC3-SMRT complex in solution.

Abdelkarim Hazem H   Brunsteiner Michael M   Neelarapu Raghupathi R   Bai He H   Madriaga Antonett A   van Breemen Richard B RB   Blond Sylvie Y SY   Gaponenko Vadim V   Petukhov Pavel A PA  

ACS chemical biology 20131002 11


Histone deacetylase 3 (HDAC3) is a promising epigenetic drug target for multiple therapeutic applications. Direct interaction between the Deacetylase Activating Domain of the silencing mediator for retinoid or thyroid-hormone receptors (SMRT-DAD) is required for activation of enzymatic activity of HDAC3. The structure of this complex and the nature of interactions with HDAC inhibitors in solution are unknown. Using novel photoreactive HDAC probes, "nanorulers", we determined the distance between  ...[more]

Similar Datasets

| S-EPMC212716 | biostudies-literature
| S-EPMC6787188 | biostudies-literature
| S-EPMC8880673 | biostudies-literature
| S-EPMC8537375 | biostudies-literature
| S-EPMC4915659 | biostudies-literature
| S-EPMC2570880 | biostudies-literature
| S-EPMC5797098 | biostudies-literature
2022-02-26 | GSE197337 | GEO
| S-EPMC2672561 | biostudies-literature
| S-EPMC7246026 | biostudies-literature