| First Author | Faouzi A | Year | 2023 |
| Journal | Nature | Volume | 613 |
| Issue | 7945 | Pages | 767-774 |
| PubMed ID | 36450356 | Mgi Jnum | J:340485 |
| Mgi Id | MGI:7525499 | Doi | 10.1038/s41586-022-05588-y |
| Citation | Faouzi A, et al. (2023) Structure-based design of bitopic ligands for the micro-opioid receptor. Nature 613(7945):767-774 |
| abstractText | Mu-opioid receptor (microOR) agonists such as fentanyl have long been used for pain management, but are considered a major public health concern owing to their adverse side effects, including lethal overdose(1). Here, in an effort to design safer therapeutic agents, we report an approach targeting a conserved sodium ion-binding site(2) found in microOR(3) and many other class A G-protein-coupled receptors with bitopic fentanyl derivatives that are functionalized via a linker with a positively charged guanidino group. Cryo-electron microscopy structures of the most potent bitopic ligands in complex with microOR highlight the key interactions between the guanidine of the ligands and the key Asp(2.50) residue in the Na(+) site. Two bitopics (C5 and C6 guano) maintain nanomolar potency and high efficacy at G(i) subtypes and show strongly reduced arrestin recruitment-one (C6 guano) also shows the lowest G(z) efficacy among the panel of microOR agonists, including partial and biased morphinan and fentanyl analogues. In mice, C6 guano displayed microOR-dependent antinociception with attenuated adverse effects, supporting the microOR sodium ion-binding site as a potential target for the design of safer analgesics. In general, our study suggests that bitopic ligands that engage the sodium ion-binding pocket in class A G-protein-coupled receptors can be designed to control their efficacy and functional selectivity profiles for G(i), G(o) and G(z) subtypes and arrestins, thus modulating their in vivo pharmacology. |
