Investigation of the role of AT1 receptor biased agonists at formation of signalin...
| Full text | |
| Author(s): |
Costa-Neto, Claudio M.
;
Parreiras-e-Silva, Lucas T.
;
Bouvier, Michel
Total Authors: 3
|
| Document type: | Review article |
| Source: | MOLECULAR PHARMACOLOGY; v. 90, n. 5, p. 587-595, NOV 1 2016. |
| Web of Science Citations: | 34 |
| Abstract | |
When studying G protein-coupled receptor (GPCR) signaling and ligand-biased agonism, at least three dimensional spaces must be considered, as follows: 1) the distinct conformations that can be stabilized by different ligands promoting the engagement of different signaling effectors and accessory regulators; 2) the distinct subcellular trafficking that can be conferred by different ligands, which results in spatially distinct signals; and 3) the differential binding kinetics that maintain the receptor in specific conformation and/or subcellular localization for different periods of time, allowing for the engagement of distinct signaling effector subsets. These three pluridimensional aspects of signaling contribute to different faces of functional selectivity and provide a complex, interconnected way to define the signaling profile of each individual ligand acting at GPCRs. In this review, we discuss how each of these aspects may contribute to the diversity of signaling, but also how they shed light on the complexity of data analyses and interpretation. The impact of phenotype variability as a source of signaling diversity, and the influence of novel and more sensitive assays in the detection and analysis of signaling pluridimensionality, is also discussed. Finally, we discuss perspectives for the use of the concept of pluridimensional signaling in drug discovery, in which we highlight future predictive tools that may facilitate the identification of compounds with optimal therapeutic and safety properties based on the signaling signatures of drug candidates. (AU) | |
| FAPESP's process: | 15/50086-4 - Development of biosensors for monitoring signaling in subcellular compartments: a powerful molecular tool for drug discovery |
| Grantee: | Claudio Miguel da Costa Neto |
| Support type: | Regular Research Grants |
| FAPESP's process: | 12/20148-0 - Development of new ligands/drugs with selective agonism action (biased agonism) for receptors of the renin-angiotensin and kallikrein-kinin systems: new properties and new biotechnological applications |
| Grantee: | Claudio Miguel da Costa Neto |
| Support type: | Research Projects - Thematic Grants |