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Structural basis of ligand selectivity and disease mutations in cysteinyl leukotriene receptors.

Authors :
Gusach A
Luginina A
Marin E
Brouillette RL
Besserer-Offroy É
Longpré JM
Ishchenko A
Popov P
Patel N
Fujimoto T
Maruyama T
Stauch B
Ergasheva M
Romanovskaia D
Stepko A
Kovalev K
Shevtsov M
Gordeliy V
Han GW
Katritch V
Borshchevskiy V
Sarret P
Mishin A
Cherezov V
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.

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