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- W2336703546 abstract "The prediction of various GPCR conformations along their activation pathways has been a challenge for computationalbiophysicists. The shortage of exptl. active structures has impaired the study of GPCR activation mechanisms. We havedeveloped a hybrid computational method that predicts multiple GPCR conformations systematically, including the active ones.This is one of the very few methods that can predict the high-energy active conformations, capable of coupling to the Gprotein, starting from an inactive conformation. We are also able to generate, to the best of our knowledge, the first quant.energy profile of GPCR activation consistent with the qual. energy landscape from expts. Our hybrid approach startswith conformational sampling over a large landscape using a coarse grid of helix tilts and rotations in the membrane. It thenselects lowest- energy conformations in the inactive- state and potential active-state energy wells defined by the TM3-TM6intracellular end distance, which is a simple but reasonable activation coordinate. These conformations are then subjected tolocal sampling on a fine grid of helix tilts and rotations. This hierarchical sampling is able to identify high-energy active- stateconformations seen in crystal structures, because those conformations still reside in their local energy wells. The lowest-energyconformations in each of the distinct energy wells are subjected to mol. dynamics (MD) simulation in explicitmembrane for local relaxation. We have validated the method with β_2 adrenergic (hβ_2AR) and M2 muscarinic acetylcholinereceptors, which have both active- and inactive- state crystal structures available. Interaction energy anal. of MD trajectories isable to reproduce key features of the qual. energy landscape of hβ_2AR activation presented in exptl. studies [Manglik et al.,2015, Cell 161, 1101]. We have also applied this methodol. to a GPCR with unknown exptl. structure, the human somatostatinreceptor subtype 5. We are able to identify the agonist- GPCR and Gα-GPCR interactions crit. in its activation, and alsogenerate a quant. energy profile consistent with exptl. observations that both the agonist and the G protein are needed tostabilize the active state. These results demonstrate our method's ability to predict the active conformations and the energylandscape of activation of GPCRs, which provides detailed structural insights into GPCR function." @default.
- W2336703546 created "2016-06-24" @default.
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- W2336703546 date "2016-03-01" @default.
- W2336703546 modified "2023-09-27" @default.
- W2336703546 title "Towards an energy landscape of G protein-coupled receptor (GPCR) activation using hybrid methods" @default.
- W2336703546 hasPublicationYear "2016" @default.
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