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Structure-based mechanism of cysteinyl leukotriene receptor inhibition by antiasthmatic drugs
A. Luginina, A. Gusach, E. Marin, A. Mishin, R. Brouillette, P. Popov, A. Shiriaeva, É. Besserer-Offroy, JM. Longpré, E. Lyapina, A. Ishchenko, N. Patel, V. Polovinkin, N. Safronova, A. Bogorodskiy, E. Edelweiss, H. Hu, U. Weierstall, W. Liu, A....
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.
Grant support
R01 GM124152
NIGMS NIH HHS - United States
NLK
Directory of Open Access Journals
from 2015
Freely Accessible Science Journals
from 2015
PubMed Central
from 2015
Europe PubMed Central
from 2015
Open Access Digital Library
from 2015-01-01
Open Access Digital Library
from 2015-01-01
- MeSH
- Leukotriene Antagonists chemistry metabolism MeSH
- Anti-Asthmatic Agents chemistry metabolism MeSH
- Chromones chemistry metabolism MeSH
- Crystallography, X-Ray MeSH
- Humans MeSH
- Ligands MeSH
- Receptors, Leukotriene chemistry genetics metabolism MeSH
- Recombinant Proteins biosynthesis chemistry isolation & purification MeSH
- Molecular Docking Simulation MeSH
- Sodium chemistry metabolism MeSH
- Protein Structure, Tertiary MeSH
- Tosyl Compounds chemistry metabolism MeSH
- Binding Sites MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, U.S. Gov't, Non-P.H.S. MeSH
The G protein-coupled cysteinyl leukotriene receptor CysLT1R mediates inflammatory processes and plays a major role in numerous disorders, including asthma, allergic rhinitis, cardiovascular disease, and cancer. Selective CysLT1R antagonists are widely prescribed as antiasthmatic drugs; however, these drugs demonstrate low effectiveness in some patients and exhibit a variety of side effects. To gain deeper understanding into the functional mechanisms of CysLTRs, we determined the crystal structures of CysLT1R bound to two chemically distinct antagonists, zafirlukast and pranlukast. The structures reveal unique ligand-binding modes and signaling mechanisms, including lateral ligand access to the orthosteric pocket between transmembrane helices TM4 and TM5, an atypical pattern of microswitches, and a distinct four-residue-coordinated sodium site. These results provide important insights and structural templates for rational discovery of safer and more effective drugs.
Institut de Biologie Structurale J P Ebel Université Grenoble Alpes CEA CNRS Grenoble 38000 France
Linac Coherent Light Source SLAC National Accelerator Laboratory Menlo Park CA 94025 USA
References provided by Crossref.org
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- $a The G protein-coupled cysteinyl leukotriene receptor CysLT1R mediates inflammatory processes and plays a major role in numerous disorders, including asthma, allergic rhinitis, cardiovascular disease, and cancer. Selective CysLT1R antagonists are widely prescribed as antiasthmatic drugs; however, these drugs demonstrate low effectiveness in some patients and exhibit a variety of side effects. To gain deeper understanding into the functional mechanisms of CysLTRs, we determined the crystal structures of CysLT1R bound to two chemically distinct antagonists, zafirlukast and pranlukast. The structures reveal unique ligand-binding modes and signaling mechanisms, including lateral ligand access to the orthosteric pocket between transmembrane helices TM4 and TM5, an atypical pattern of microswitches, and a distinct four-residue-coordinated sodium site. These results provide important insights and structural templates for rational discovery of safer and more effective drugs.
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