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Constraints on GPCR Heterodimerization Revealed by the Type-4 Induced-Association BRET Assay
G-protein-coupled receptors (GPCRs) comprise the largest and most pharmacologically important family of cell-surface receptors encoded by the human genome. In many instances, the distinct signaling behavior of certain GPCRs has been explained in terms of the formation of heteromers with, for example...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Biophysical Society
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341220/ https://www.ncbi.nlm.nih.gov/pubmed/30558888 http://dx.doi.org/10.1016/j.bpj.2018.09.034 |