Enhancing the Signaling of GPCRs via Orthosteric Ions-Reference-Cited by-同舟云学术

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Enhancing the Signaling of GPCRs via Orthosteric Ions

Published:2020-01-23 Issue:2 Volume:6 Page:274-282
ISSN:2374-7943
Container-title:ACS Central Science
language:en
Short-container-title:ACS Cent. Sci.

Author:

Chan H. C. Stephen¹,Xu Yueming²,Tan Liang²,Vogel Horst¹³^ORCID,Cheng Jianjun²^ORCID,Wu Dong²,Yuan Shuguang¹^ORCID

Affiliation:

1. Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China

2. iHuman Institute, ShanghaiTech University, Shanghai 201210, China

3. Institute of Chemical Sciences and Engineering, Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne 1015, Switzerland

Funder

Shenzhen Institutes of Advanced Technology, CAS

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acscentsci.9b01247

Reference60 articles.

1. Allosteric sodium in class A GPCR signaling

2. The Role of a Sodium Ion Binding Site in the Allosteric Modulation of the A2A Adenosine G Protein-Coupled Receptor

3. The 2.1 Å Resolution Structure of Cyanopindolol-Bound β1-Adrenoceptor Identifies an Intramembrane Na+ Ion that Stabilises the Ligand-Free Receptor

4. D 4 dopamine receptor high-resolution structures enable the discovery of selective agonists

5. Serial millisecond crystallography for routine room-temperature structure determination at synchrotrons

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