Cargando…
Structure-guided development of heterodimer-selective GPCR ligands
Crystal structures of G protein-coupled receptor (GPCR) ligand complexes allow a rational design of novel molecular probes and drugs. Here we report the structure-guided design, chemical synthesis and biological investigations of bivalent ligands for dopamine D(2) receptor/neurotensin NTS(1) recepto...
Autores principales: | Hübner, Harald, Schellhorn, Tamara, Gienger, Marie, Schaab, Carolin, Kaindl, Jonas, Leeb, Laurin, Clark, Timothy, Möller, Dorothee, Gmeiner, Peter |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4963535/ https://www.ncbi.nlm.nih.gov/pubmed/27457610 http://dx.doi.org/10.1038/ncomms12298 |
Ejemplares similares
-
Structure-Based Evolution of Subtype-Selective Neurotensin Receptor Ligands
por: Schaab, Carolin, et al.
Publicado: (2014) -
Active-State Models of Ternary GPCR Complexes: Determinants of Selective Receptor-G-Protein Coupling
por: Kling, Ralf C., et al.
Publicado: (2013) -
Allosteric ligands control the activation of a class C GPCR heterodimer by acting at the transmembrane interface
por: Liu, Lei, et al.
Publicado: (2021) -
Visualization of ligand-induced dopamine D(2S) and D(2L) receptor internalization by TIRF microscopy
por: Tabor, Alina, et al.
Publicado: (2017) -
Structure-based development of caged dopamine D(2)/D(3) receptor antagonists
por: Gienger, Marie, et al.
Publicado: (2020)