All living organisms face a variety of environmental stresses that cause the misfolding and aggregation of proteins. To eliminate damaged proteins, cells developed highly efficient stress response and protein quality control systems. We performed a biochemical and structural analysis of the bacterial CtsR/McsB stress response. The crystal structure of the CtsR repressor, in complex with DNA, pinpointed key residues important for high-affinity binding to the promoter regions of heat-shock genes. Moreover, biochemical characterization of McsB revealed that McsB specifically phosphorylates arginine residues in the DNA binding domain of CtsR, thereby impairing its function as a repressor of stress response genes. Identification of the CtsR/McsB arginine phospho-switch expands the repertoire of possible protein modifications involved in prokaryotic and eukaryotic transcriptional regulation.
Protein
arginine deiminases (PADs) are calcium-dependent histone-modifying
enzymes whose activity is dysregulated in inflammatory diseases and
cancer. PAD2 functions as an Estrogen Receptor (ER) coactivator in
breast cancer cells via the citrullination of histone tail arginine
residues at ER binding sites. Although an attractive therapeutic target,
the mechanisms that regulate PAD2 activity are largely unknown, especially
the detailed role of how calcium facilitates enzyme activation. To
gain insights into these regulatory processes, we determined the first
structures of PAD2 (27 in total), and through calcium-titrations by
X-ray crystallography, determined the order of binding and affinity
for the six calcium ions that bind and activate this enzyme. These
structures also identified several PAD2 regulatory elements, including
a calcium switch that controls proper positioning of the catalytic
cysteine residue, and a novel active site shielding mechanism. Additional
biochemical and mass-spectrometry-based hydrogen/deuterium exchange
studies support these structural findings. The identification of multiple
intermediate calcium-bound structures along the PAD2 activation pathway
provides critical insights that will aid the development of allosteric
inhibitors targeting the PADs.
Nurr1/NR4A2 is an orphan nuclear receptor, and currently there are no known natural ligands that bind Nurr1. A recent metabolomics study identified unsaturated fatty acids, including arachidonic acid and docosahexaenoic acid (DHA), that interact with the ligand-binding domain (LBD) of a related orphan receptor, Nur77/NR4A1. However, the binding location and whether these ligands bind other NR4A receptors were not defined. Here, we show that unsaturated fatty acids also interact with the Nurr1 LBD, and solution NMR spectroscopy reveals the binding epitope of DHA at its putative ligand-binding pocket. Biochemical assays reveal that DHA-bound Nurr1 interacts with high affinity with a peptide derived from PIASγ, a protein that interacts with Nurr1 in cellular extracts, and DHA also affects cellular Nurr1 transactivation. This work is the first structural report of a natural ligand binding to a canonical NR4A ligand-binding pocket, and indicates a natural ligand can bind and affect Nurr1 function.
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