↓ Skip to main content

G Protein-Coupled Receptors in Drug Discovery

Overview of attention for book
G Protein-Coupled Receptors in Drug Discovery
Springer New York

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Purification of Stabilized GPCRs for Structural and Biophysical Analyses
  3. Altmetric Badge
    Chapter 2 Purification and Crystallization of a Thermostabilized Agonist-Bound Conformation of the Human Adenosine A 2A Receptor
  4. Altmetric Badge
    Chapter 3 2D Projection Analysis of GPCR Complexes by Negative Stain Electron Microscopy
  5. Altmetric Badge
    Chapter 4 Nuts and Bolts of CF 3 and CH 3 NMR Toward the Understanding of Conformational Exchange of GPCRs
  6. Altmetric Badge
    Chapter 5 Single-Molecule Fluorescence Microscopy for the Analysis of Fast Receptor Dynamics
  7. Altmetric Badge
    Chapter 6 Quantitative Multi-color Detection Strategies for Bioorthogonally Labeled GPCRs
  8. Altmetric Badge
    Chapter 7 Approaches to Characterize and Quantify Oligomerization of GPCRs
  9. Altmetric Badge
    Chapter 8 Monitoring G Protein Activation in Cells with BRET
  10. Altmetric Badge
    Chapter 9 Use of Fluorescence Indicators in Receptor Ligands
  11. Altmetric Badge
    Chapter 10 Detection and Quantification of Intracellular Signaling Using FRET-Based Biosensors and High Content Imaging
  12. Altmetric Badge
    Chapter 11 The Measurement of Receptor Signaling Bias
  13. Altmetric Badge
    Chapter 12 Approaches to Assess Functional Selectivity in GPCRs: Evaluating G Protein Signaling in an Endogenous Environment
  14. Altmetric Badge
    Chapter 13 Bioluminescence Resonance Energy Transfer Approaches to Discover Bias in GPCR Signaling
  15. Altmetric Badge
    Chapter 14 Virus-Mediated Expression of DREADDs for In Vivo Metabolic Studies
  16. Altmetric Badge
    Chapter 15 High-Throughput Screening for Allosteric Modulators of GPCRs
  17. Altmetric Badge
    Chapter 16 Radioligand Binding Assay for an Exon 11-Associated Mu Opioid Receptor Target
  18. Altmetric Badge
    Chapter 17 Docking and Virtual Screening Strategies for GPCR Drug Discovery
  19. Altmetric Badge
    Chapter 18 The Dynamic Process of Drug–GPCR Binding at Either Orthosteric or Allosteric Sites Evaluated by Metadynamics
  20. Altmetric Badge
    Chapter 19 Experiment-Guided Molecular Modeling of Protein–Protein Complexes Involving GPCRs
  21. Altmetric Badge
    Chapter 20 Interaction Fingerprints and Their Applications to Identify Hot Spots
Attention for Chapter 6: Quantitative Multi-color Detection Strategies for Bioorthogonally Labeled GPCRs
Altmetric Badge

Readers on

mendeley
6 Mendeley
You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output. Click here to find out more.
Chapter title
Quantitative Multi-color Detection Strategies for Bioorthogonally Labeled GPCRs
Chapter number 6
Book title
G Protein-Coupled Receptors in Drug Discovery
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-2914-6_6
Pubmed ID
Book ISBNs
978-1-4939-2913-9, 978-1-4939-2914-6
Authors

Minyoung Park, He Tian, Saranga Naganathan, Thomas P. Sakmar, Thomas Huber, Park, Minyoung, Tian, He, Naganathan, Saranga, Sakmar, Thomas P., Huber, Thomas

Abstract

We describe multiple bioorthogonal approaches to label G protein-coupled receptors (GPCRs) heterologously expressed in mammalian cells. The use of genetically encoded unnatural amino acids as bioorthogonal tags results in receptors that are expressed at lower levels than even their low abundance wild-type counterparts. Therefore, reproducible and sensitive quantification of the labeled GPCRs is extremely important and conventional methods are simply not sufficiently accurate and precise. Silver stains lack reproducibility, spectroscopic methods using fluorescent ligands are limited to quantifying only functional receptor molecules, and immunoassays using epitope tags derived from rhodopsin are particularly variable for low-abundance GPCRs. To avoid these shortcomings, we employ near infrared (NIR) imaging-based methods that enable simultaneous multi-color detection of two different antigens, thus facilitating the ratiometric analysis of bioorthogonally modified GPCRs. We anticipate that these multi-color detection strategies will provide new tools for quantitatively assessing stoichiometrically labeled GPCRs for studies of signalosomes and for structure-function relationships at a single molecule level.

Timeline

Login to access the full chart related to this output.

If you don’t have an account, click here to discover Explorer

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 6 100%

Demographic breakdown

Readers by professional status Count As %
Professor 1 17%
Student > Ph. D. Student 1 17%
Professor > Associate Professor 1 17%
Student > Bachelor 1 17%
Unknown 2 33%
Readers by discipline Count As %
Neuroscience 2 33%
Biochemistry, Genetics and Molecular Biology 1 17%
Pharmacology, Toxicology and Pharmaceutical Science 1 17%
Unknown 2 33%