Ligand and receptor dynamics contribute to the mechanism of graded PPARγ agonism.
Ligand and receptor dynamics contribute to the mechanism of graded PPARγ agonism.
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DOI:
10.1016/j.str.2011.10.018
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发表时间:
2012-01-11
期刊:
影响因子:
5.7
通讯作者:
Kojetin, Douglas J.
中科院分区:
文献类型:
--
作者:
Hughes, Travis S.;Chalmers, Michael J.;Novick, Scott;Kuruvilla, Dana S.;Chang, Mi Ra;Kamenecka, Theodore M.;Rance, Mark;Johnson, Bruce A.;Burris, Thomas P.;Griffin, Patrick R.;Kojetin, Douglas J.
Ligand binding to proteins is not a static process, but rather involves a number of complex dynamic transitions. A flexible ligand can change conformation upon binding its target. The conformation and dynamics of a protein can change to facilitate ligand binding. The conformation of the ligand, however, is generally presumed to have one primary binding mode, shifting the protein conformational ensemble from one state to another. We report solution NMR studies that reveal peroxisome proliferator-activated receptor γ (PPARγ) modulators can sample multiple binding modes manifesting in multiple receptor conformations in slow conformational exchange. Our NMR, hydrogen/deuterium exchange and docking studies reveal that ligand-induced receptor stabilization and binding mode occupancy correlate with the graded agonist response of the ligand. Our results suggest that ligand and receptor dynamics affect the graded transcriptional output of PPARγ modulators.
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影响因子:
14.8
作者:
Bruning, John B.;Parent, Alexander A.;Gil, German;Zhao, Min;Nowak, Jason;Pace, Margaret C.;Smith, Carolyn L.;Afonine, Pavel V.;Adams, Paul D.;Katzenellenbogen, John A.;Nettles, Kendall W.
通讯作者:
Nettles, Kendall W.
影响因子:
64.8
作者:
通讯作者:
--
DOI:
10.1056/nejmcibr1012075
发表时间:
2010-12-30
期刊:
The New England journal of medicine
影响因子:
--
作者:
Kahn BB;McGraw TE
通讯作者:
McGraw TE
DOI:
10.1016/j.bbrc.2007.10.143
发表时间:
2008-01-04
影响因子:
3.1
作者:
Lu, Jianyun;Chen, Minghe;Li, Ellen
通讯作者:
Li, Ellen
影响因子:
8
作者:
Hamuro, Yoshitomo;Coales, Stephen J.;Griffin, Patrick R.
通讯作者:
Griffin, Patrick R.