Immobilization of arrestin-3 on different biosensor platforms for evaluating GPCR binding-Reference-Cited by-同舟云学术

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Immobilization of arrestin-3 on different biosensor platforms for evaluating GPCR binding

Published:2020 Issue:41 Volume:22 Page:24086-24096
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Avsar Saziye Yorulmaz¹²³⁴,Kapinos Larisa E.⁵²⁶⁴,Schoenenberger Cora-Ann¹²³⁴^ORCID,Schertler Gebhard F. X.⁷⁸⁹¹⁰⁴^ORCID,Mühle Jonas⁷⁸⁹¹⁰⁴,Meger Benoit⁷⁸⁹¹⁰⁴,Lim Roderick Y. H.⁵²⁶⁴^ORCID,Ostermaier Martin K.⁹¹⁰⁴^ORCID,Lesca Elena⁷⁸⁹¹⁰⁴,Palivan Cornelia G.¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry and the Swiss Nanoscience Institute

2. University of Basel

3. 4002 Basel

4. Switzerland

5. Biozentrum and the Swiss Nanoscience Institute

6. 4056 Basel

7. Department of Biology and Chemistry

8. Laboratory of Biomolecular Research

9. Paul Scherrer Institute

10. 5303 Villigen-PSI

Abstract

Label free, biosensor-based screening approaches can be easily adapted for testing interactions of arrestins with different GPCRs.

Funder

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Universität Basel

Swiss Nanoscience Institute

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2020/CP/D0CP01464H

Reference48 articles.

1. Structural diversity of G protein-coupled receptors and significance for drug discovery

2. Diverse activation pathways in class A GPCRs converge near the G-protein-coupling region

3. How Ligands Illuminate GPCR Molecular Pharmacology

4. Structure of the M2 muscarinic receptor–β-arrestin complex in a lipid nanodisc

5. V. V. Gurevich and E. V.Gurevich , Advances in Protein Chemistry and Structural Biology , Elsevier , 2020 , vol. 121, pp. 169–197

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