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Towards high throughput GPCR crystallography: In Meso soaking of Adenosine A2A Receptor crystals.


ABSTRACT: Here we report an efficient method to generate multiple co-structures of the A2A G protein-coupled receptor (GPCR) with small-molecules from a single preparation of a thermostabilised receptor crystallised in Lipidic Cubic Phase (LCP). Receptor crystallisation is achieved following purification using a low affinity "carrier" ligand (theophylline) and crystals are then soaked in solutions containing the desired (higher affinity) compounds. Complete datasets to high resolution can then be collected from single crystals and seven structures are reported here of which three are novel. The method significantly improves structural throughput for ligand screening using stabilised GPCRs, thereby actively driving Structure-Based Drug Discovery (SBDD).

SUBMITTER: Rucktooa P 

PROVIDER: S-EPMC5758569 | biostudies-literature | 2018 Jan

REPOSITORIES: biostudies-literature

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Towards high throughput GPCR crystallography: In Meso soaking of Adenosine A<sub>2A</sub> Receptor crystals.

Rucktooa Prakash P   Cheng Robert K Y RKY   Segala Elena E   Geng Tian T   Errey James C JC   Brown Giles A GA   Cooke Robert M RM   Marshall Fiona H FH   Doré Andrew S AS  

Scientific reports 20180108 1


Here we report an efficient method to generate multiple co-structures of the A<sub>2A</sub> G protein-coupled receptor (GPCR) with small-molecules from a single preparation of a thermostabilised receptor crystallised in Lipidic Cubic Phase (LCP). Receptor crystallisation is achieved following purification using a low affinity "carrier" ligand (theophylline) and crystals are then soaked in solutions containing the desired (higher affinity) compounds. Complete datasets to high resolution can then  ...[more]

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