Skip to main content

Fluorescence Anisotropy-Based Assay for Characterization of Ligand Binding Dynamics to GPCRs: The Case of Cy3B-Labeled Ligands Binding to MC4 Receptors in Budded Baculoviruses

Part of the Methods in Molecular Biology book series (MIMB,volume 2268)

Abstract

During the past decade, fluorescence methods have become valuable tools for characterizing ligand binding to G protein-coupled receptors (GPCRs). However, only a few of the assays enable studying wild-type receptors and monitor the ligand binding in real time. One of the approaches that is inherently suitable for this purpose is the fluorescence anisotropy (FA) assay. In the FA assay, the change of ligand’s rotational freedom connected with its binding to the receptor can be monitored with a conventional fluorescence plate reader equipped with suitable optical filters. To achieve the high receptor concentration required for the assay and the low autofluorescence levels essential for reliable results, budded baculoviruses that display GPCRs on their surfaces can be used. The monitoring process generates a substantial amount of kinetic data, which is usually stored as a proprietary file format limiting the flexibility of data analysis. To solve this problem, we propose the use of the data curation software Aparecium (http://gpcr.ut.ee/aparecium.html), which integrates experimental data with metadata in a Minimum Information for Data Analysis in Systems Biology (MIDAS) format. Aparecium enables data export to different software packages for fitting to suitable kinetic or equilibrium models. A combination of the FA assay with the novel data analysis strategy is suitable for screening new active compounds, but also for modeling complex systems of ligand binding to GPCRs. We present the proposed approach using different fluorescent probes and assay types to characterize ligand binding to melanocortin 4 (MC4) receptor.

Key words

  • Budded baculoviruses
  • Fluorescence anisotropy
  • Melanocortin 4 receptor
  • Global analysis
  • Binding kinetics

This is a preview of subscription content, access via your institution.

Buying options

Protocol
USD   49.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   99.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD   129.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD   199.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

Springer Nature is developing a new tool to find and evaluate Protocols. Learn more

References

  1. Hoffmann C, Castro M, Rinken A, Leurs R, Hill SJ, Vischer HF (2015) Ligand residence time at G-protein-coupled receptors - why we should take our time to study it. Mol Pharmacol 88:552–560

    CrossRef  CAS  Google Scholar 

  2. Soave M, Briddon SJ, Hill SJ, Stoddart LA (2020) Fluorescent ligands: bringing light to emerging GPCR paradigms. Br J Pharmacol 177:978–991

    CrossRef  CAS  Google Scholar 

  3. Perrin F (1926) Polarisation de la lumičre de fluorescence. Vie moyenne des molécules dans l’etat excité. J Phys Radium 7:390–410

    CrossRef  CAS  Google Scholar 

  4. Vernall AJ, Hill SJ, Kellam B (2014) The evolving small-molecule fluorescent-conjugate toolbox for Class A GPCRs. Br J Pharmacol 171:1073–1084

    CrossRef  CAS  Google Scholar 

  5. Rinken A, Lavogina D, Kopanchuk S (2018) Assays with detection of fluorescence anisotropy: challenges and possibilities to characterize ligand binding to GPCRs. Trends Pharmacol Sci 39:187–199

    CrossRef  CAS  Google Scholar 

  6. Nosjean O, Souchaud S, Deniau C, Geneste O, Cauquil N, Boutin JA (2006) A simple theoretical model for fluorescence polarization binding assay development. J Biomol Screen 11:949–958

    CrossRef  CAS  Google Scholar 

  7. Veiksina S, Kopanchuk S, Rinken A (2010) Fluorescence anisotropy assay for pharmacological characterization of ligand binding dynamics to melanocortin 4 receptors. Anal Biochem 402:32–39

    CrossRef  CAS  Google Scholar 

  8. Veiksina S, Kopanchuk S, Rinken A (2014) Budded baculoviruses as a tool for a homogeneous fluorescence anisotropy-based assay of ligand binding to G protein-coupled receptors: the case of melanocortin 4 receptors. Biochim Biophys Acta 1838:372–381

    CrossRef  CAS  Google Scholar 

  9. Kost TA, Condreay JP, Jarvis DL (2005) Baculovirus as versatile vectors for protein expression in insect and mammalian cells. Nat Biotechnol 23:567–575

    CrossRef  CAS  Google Scholar 

  10. Wang Q, Bosch BJ, Vlak JM, van Oers MM, Rottier PJ, van Lent JWM (2016) Budded baculovirus particle structure revisited. J Invert Pathol 134:15–22

    CrossRef  Google Scholar 

  11. Kost TA, Condreay JP, Ames RS (2010) Baculovirus gene delivery: a flexible assay development tool. Curr Gene Ther 10:168–173

    CrossRef  CAS  Google Scholar 

  12. Roehrl MH, Wang JY, Wagner G (2004) A general framework for development and data analysis of competitive high-throughput screens for small-molecule inhibitors of protein-protein interactions by fluorescence polarization. Biochemistry 43:16056–16066

    CrossRef  CAS  Google Scholar 

  13. Jameson DM, Mocz G (2005) Fluorescence polarization/anisotropy approaches to study protein-ligand interactions: effects of errors and uncertainties. Methods Mol Biol 305:301–322

    CAS  PubMed  Google Scholar 

  14. Rinken A, Veiksina S, Kopanchuk S (2016) Dynamics of ligand binding to GPCR: Residence time of melanocortins and its modulation. Pharmacol Res 113:747–753

    CrossRef  CAS  Google Scholar 

  15. Tõntson L, Kopanchuk S, Rinken A (2014) Characterization of 5-HT1A receptors and their complexes with G-proteins in budded baculovirus particles using fluorescence anisotropy of Bodipy-FL-NAN-190. Neurochem Int 67:32–38

    CrossRef  Google Scholar 

  16. Allikalt A, Kopanchuk S, Rinken A (2018) Implementation of fluorescence anisotropy-based assay for the characterization of ligand binding to dopamine D1 receptors. Eur J Pharmacol 839:40–46

    CrossRef  CAS  Google Scholar 

  17. Scodeller P, Simon-Gracia L, Kopanchuk S, Tobi A, Kilk K, Säälik P, Kurm K, Squadrito ML, Kotamraju VR, Rinken A, De Palma M, Ruoslahti E, Teesalu T (2017) Precision targeting of tumor macrophages with a CD206 binding peptide. Sci Rep 7:14655

    CrossRef  Google Scholar 

  18. Sormus T, Lavogina D, Enkvist E, Uri A, Viht K (2019) Efficient photocaging of a tight-binding bisubstrate inhibitor of cAMP-dependent protein kinase. Chem Commun (Camb) 55:11147–11150

    CrossRef  CAS  Google Scholar 

  19. Kopanchuk S, Veiksina S, Mutulis F, Mutule I, Yahorava S, Mandrika I, Petrovska R, Rinken A, Wikberg JES (2006) Kinetic evidence for tandemly arranged ligand binding sites in melanocortin 4 receptor complexes. Neurochem Int 49:533–542

    CrossRef  CAS  Google Scholar 

  20. Link R, Veiksina S, Rinken A, Kopanchuk S (2017) Characterization of ligand binding to melanocortin 4 receptors using fluorescent peptides with improved kinetic properties. Eur J Pharmacol 799:58–66

    CrossRef  CAS  Google Scholar 

  21. Laasfeld T, Kopanchuk S, Rinken A (2017) Image-based cell-size estimation for baculovirus quantification. BioTechniques 63:161–168

    CrossRef  CAS  Google Scholar 

  22. Thompson RB, Gryczynski I, Malicka J (2002) Fluorescence polarization standards for high-throughput screening and imaging. BioTechniques 32:34–42

    CrossRef  CAS  Google Scholar 

  23. Link R, Veiksina S, Tahk MJ, Laasfeld T, Paiste P, Kopanchuk S, Rinken A (2020) The constitutive activity of melanocortin-4 receptors in cAMP pathway is allosterically modulated by zinc and copper ions. J Neurochem 153:346–361

    CrossRef  CAS  Google Scholar 

  24. Veiksina S, Kopanchuk S, Mazina O, Link R, Lille A, Rinken A (2015) Homogeneous fluorescence anisotropy-based assay for characterization of ligand binding dynamics to gpcrs in budded baculoviruses: the case of Cy3B-NDP-alpha-MSH binding to MC4 receptors. Methods Mol Biol 1272:37–50

    CrossRef  CAS  Google Scholar 

  25. Beechem JM, Gratton E, Ameloot M, Knutson JR, Brand L (2002) The global analysis of fluorescence intensity and anisotropy decay data: second-generation theory and programs. In: Lakowicz JR (ed) Topics in fluorescence spectroscopy: principles. Springer, Boston, MA, pp 241–305

    CrossRef  Google Scholar 

Download references

Acknowledgments

The work has been financed by the Estonian Ministry of Education and Science (PSG230) and by the NATO (SPS 985261).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ago Rinken .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and Permissions

Copyright information

© 2021 Springer Science+Business Media, LLC, part of Springer Nature

About this protocol

Check for updates. Verify currency and authenticity via CrossMark

Cite this protocol

Veiksina, S., Tahk, MJ., Laasfeld, T., Link, R., Kopanchuk, S., Rinken, A. (2021). Fluorescence Anisotropy-Based Assay for Characterization of Ligand Binding Dynamics to GPCRs: The Case of Cy3B-Labeled Ligands Binding to MC4 Receptors in Budded Baculoviruses. In: Martins, S.A.M., Prazeres, D.M.F. (eds) G Protein-Coupled Receptor Screening Assays. Methods in Molecular Biology, vol 2268. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-1221-7_8

Download citation

  • DOI: https://doi.org/10.1007/978-1-0716-1221-7_8

  • Published:

  • Publisher Name: Humana, New York, NY

  • Print ISBN: 978-1-0716-1220-0

  • Online ISBN: 978-1-0716-1221-7

  • eBook Packages: Springer Protocols