Please use this identifier to cite or link to this item: https://doi.org/10.3390/ijms22105242
Title: Development of phosphodiesterase–protein-kinase complexes as novel targets for discovery of inhibitors with enhanced specificity
Authors: Tulsian, Nikhil K. 
Sin, Valerie Jia-En
Koh, Hwee-Ling 
Anand, Ganesh S. 
Keywords: Fluorescence polarization
Inhibitors
Natural products
Phosphodiesterase (PDE)
Protein kinase
Selectivity
Issue Date: 15-May-2021
Publisher: MDPI AG
Citation: Tulsian, Nikhil K., Sin, Valerie Jia-En, Koh, Hwee-Ling, Anand, Ganesh S. (2021-05-15). Development of phosphodiesterase–protein-kinase complexes as novel targets for discovery of inhibitors with enhanced specificity. International Journal of Molecular Sciences 22 (10) : 5242. ScholarBank@NUS Repository. https://doi.org/10.3390/ijms22105242
Rights: Attribution 4.0 International
Abstract: Phosphodiesterases (PDEs) hydrolyze cyclic nucleotides to modulate multiple signaling events in cells. PDEs are recognized to actively associate with cyclic nucleotide receptors (protein kinases, PKs) in larger macromolecular assemblies referred to as signalosomes. Complexation of PDEs with PKs generates an expanded active site that enhances PDE activity. This facilitates signalosome-associated PDEs to preferentially catalyze active hydrolysis of cyclic nucleotides bound to PKs and aid in signal termination. PDEs are important drug targets, and current strategies for inhibitor discovery are based entirely on targeting conserved PDE catalytic domains. This often results in inhibitors with cross-reactivity amongst closely related PDEs and attendant unwanted side effects. Here, our approach targeted PDE–PK complexes as they would occur in signalosomes, thereby offering greater specificity. Our developed fluorescence polarization assay was adapted to identify inhibitors that block cyclic nucleotide pockets in PDE–PK complexes in one mode and disrupt protein-protein interactions between PDEs and PKs in a second mode. We tested this approach with three different systems—cAMP-specific PDE8–PKAR, cGMP-specific PDE5–PKG, and dualspecificity RegA–RD complexes—and ranked inhibitors according to their inhibition potency. Targeting PDE–PK complexes offers biochemical tools for describing the exquisite specificity of cyclic nucleotide signaling networks in cells. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
Source Title: International Journal of Molecular Sciences
URI: https://scholarbank.nus.edu.sg/handle/10635/232471
ISSN: 1661-6596
DOI: 10.3390/ijms22105242
Rights: Attribution 4.0 International
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