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Structural basis of ligand selectivity and disease mutations in cysteinyl leukotriene receptors.
- Source :
-
Nature communications [Nat Commun] 2019 Dec 06; Vol. 10 (1), pp. 5573. Date of Electronic Publication: 2019 Dec 06. - Publication Year :
- 2019
-
Abstract
- Cysteinyl leukotriene G protein-coupled receptors CysLT <subscript>1</subscript> and CysLT <subscript>2</subscript> regulate pro-inflammatory responses associated with allergic disorders. While selective inhibition of CysLT <subscript>1</subscript> R has been used for treating asthma and associated diseases for over two decades, CysLT <subscript>2</subscript> R has recently started to emerge as a potential drug target against atopic asthma, brain injury and central nervous system disorders, as well as several types of cancer. Here, we describe four crystal structures of CysLT <subscript>2</subscript> R in complex with three dual CysLT <subscript>1</subscript> R/CysLT <subscript>2</subscript> R antagonists. The reported structures together with the results of comprehensive mutagenesis and computer modeling studies shed light on molecular determinants of CysLTR ligand selectivity and specific effects of disease-related single nucleotide variants.
- Subjects :
- Animals
Asthma genetics
Asthma metabolism
Computer Simulation
Crystallography, X-Ray
HEK293 Cells
Humans
Leukotriene D4 metabolism
Ligands
Models, Molecular
Molecular Docking Simulation
Mutagenesis
Protein Conformation
Protein Engineering
Receptors, Leukotriene drug effects
Sf9 Cells
Mutation
Receptors, Leukotriene chemistry
Receptors, Leukotriene genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 10
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 31811124
- Full Text :
- https://doi.org/10.1038/s41467-019-13348-2