The G2S Core is the programmatic foundation and resource center of the CMPD project and activities occur at Argonne National Laboratory beamline GMCA and TSRI. G2S is staffed with an experienced team of senior scientists and full-time research technicians with a significant history of successful collaborations which led to the publication of three human GPCR structures in the past 19 months (see Figure 3 in the overall summary), namely Raymond Stevens and a team of Co-Core Directors including Drs. Ellen Chien, Vadim Cherezov and Robert Fischetti. The research is conducted at facilities at TSRI in La Jolla, California and GM/CA-CAT/APS at Argonne, Illinois. In addition, key collaborations are established with Pat Griffin at TSRI-Florida on HDX analysis of membrane proteins and So Iwata at Kyoto University and Imperial College on crystallization with antibodies (see letters of collaboration). G2S will be provided with targets that have been prioritized by Projects 1 and 3 and be responsible for gene construct design and synthesis, expression, purification, and sample characterization, crystallization, and data collection and processing. Methods of sample characterization to be employed in this core include the traditional size exclusion chromatography and gel electrophoresis, as well as the more specialized diffusion and stability analysis by LCP-FRAP, CPM and LCP-Tm, respectively. The highly purified samples that are produced will be evaluated within the Core by crystallographic and NMR methods for structure determination and analysis. Final structure refinement and results dissemination will be coordinated through Projects 1 and 3.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54GM094618-04
Application #
8501568
Study Section
Special Emphasis Panel (ZGM1-CBB-3)
Project Start
Project End
Budget Start
2013-07-01
Budget End
2014-06-30
Support Year
4
Fiscal Year
2013
Total Cost
$1,304,941
Indirect Cost
$278,154
Name
Scripps Research Institute
Department
Type
DUNS #
781613492
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Eddy, Matthew T; Gao, Zhan-Guo; Mannes, Philip et al. (2018) Extrinsic Tryptophans as NMR Probes of Allosteric Coupling in Membrane Proteins: Application to the A2A Adenosine Receptor. J Am Chem Soc 140:8228-8235
Eddy, Matthew T; Lee, Ming-Yue; Gao, Zhan-Guo et al. (2018) Allosteric Coupling of Drug Binding and Intracellular Signaling in the A2A Adenosine Receptor. Cell 172:68-80.e12
Peng, Yao; McCorvy, John D; Harpsøe, Kasper et al. (2018) 5-HT2C Receptor Structures Reveal the Structural Basis of GPCR Polypharmacology. Cell 172:719-730.e14
Seidel, Lisa; Zarzycka, Barbara; Zaidi, Saheem A et al. (2017) Structural insight into the activation of a class B G-protein-coupled receptor by peptide hormones in live human cells. Elife 6:
Zhang, Haitao; Han, Gye Won; Batyuk, Alexander et al. (2017) Structural basis for selectivity and diversity in angiotensin II receptors. Nature 544:327-332
Rowe, Timothy B; Luo, Zhe-Xi; Ketcham, Richard A et al. (2016) X-ray computed tomography datasets for forensic analysis of vertebrate fossils. Sci Data 3:160040
Ishchenko, Andrii; Cherezov, Vadim; Liu, Wei (2016) Preparation and Delivery of Protein Microcrystals in Lipidic Cubic Phase for Serial Femtosecond Crystallography. J Vis Exp :
Yang, Dehua; de Graaf, Chris; Yang, Linlin et al. (2016) Structural Determinants of Binding the Seven-transmembrane Domain of the Glucagon-like Peptide-1 Receptor (GLP-1R). J Biol Chem 291:12991-3004
Zhu, Lan; Weierstall, Uwe; Cherezov, Vadim et al. (2016) Serial Femtosecond Crystallography of Membrane Proteins. Adv Exp Med Biol 922:151-160
Leach, Katie; Gregory, Karen J; Kufareva, Irina et al. (2016) Towards a structural understanding of allosteric drugs at the human calcium-sensing receptor. Cell Res 26:574-92

Showing the most recent 10 out of 115 publications