Skip to main content
Log in

Fluorescence Characteristics of Hydrophobic Partial Agonist Probes of the Cholecystokinin Receptor

  • Original Paper
  • Published:
Bioscience Reports

Abstract

Fluorescence spectroscopic studies are powerful tools for the evaluation of receptor structure and the dynamic changes associated with receptor activation. Here, we have developed two chemically distinct fluorescent probes of the cholecystokinin (CCK) receptor by attaching acrylodan or a nitrobenzoxadiazole moiety to the amino terminus of a partial agonist CCK analogue. These two probes were able to bind to the CCK receptor specifically and with high affinity, and were able to elicit only submaximal intracellular calcium responses typical of partial agonists. The fluorescence characteristics of these probes were compared with those previously reported for structurally-related full agonist and antagonist probes. Like the previous probes, the partial agonist probes exhibited longer fluorescence lifetimes and increased anisotropy when bound to the receptor than when free in solution. The receptor-bound probes were not easily quenched by potassium iodide, suggesting that the fluorophores were protected from the extracellular aqueous milieu. The fluorescence characteristics of the partial agonist probes were quite similar to those of the analogous full agonist probes and quite distinct from the analogous antagonist probes. These data suggest that the partially activated conformational state of this receptor is more closely related to its fully active state than to its inactive state.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

Abbreviations

HPLC:

High performance liquid chromatography

NBD:

7-nitrobenz-2-oxa-1,3-diazole

CCK:

Cholecystokinin

CCKR:

Type A CCK receptor

CHO:

Chinese hamster ovary

KRH:

Krebs–Ringers-HEPES medium

aca:

Aminocaproic acid

OPE:

Gly-[(Nle28,31)CCK-26-32]-phenylethyl ester

Fura 2-AM:

Fura 2-acetoxymethyl ester

References

  1. Ji TH, Grossmann M, Ji I (1998) G protein-coupled receptors. I. Diversity of receptor-ligand interactions. J Biol Chem 273:17299–17302

    Article  PubMed  CAS  Google Scholar 

  2. Palczewski K, Kumasaka T, Hori T, Behnke CA, Motoshima H, Fox BA, Le Trong I, Teller DC, Okada T, Stenkamp RE, Yamamoto M, Miyano M (2000) Crystal structure of rhodopsin: A G protein-coupled receptor. Science 289:739–745

    Article  PubMed  CAS  Google Scholar 

  3. Hadac EM, Ji Z, Pinon DI, Henne RM, Lybrand TP, Miller LJ (1999) A peptide agonist acts by occupation of a monomeric G protein-coupled receptor: dual sites of covalent attachment to domains near TM1 and TM7 of the same molecule make biologically significant domain-swapped dimerization unlikely. J Med Chem 42:2105–2111

    Article  PubMed  CAS  Google Scholar 

  4. Dong M, Ding XQ, Pinon DI, Hadac EM, Oda RP, Landers JP, Miller LJ (1999) Structurally related peptide agonist, partial agonist, and antagonist occupy a similar binding pocket within the cholecystokinin receptor. Rapid analysis using fluorescent photoaffinity labeling probes and capillary electrophoresis. J Biol Chem 274:4778–4785

    Article  PubMed  CAS  Google Scholar 

  5. Ding XQ, Pinon DI, Furse KE, Lybrand TP, Miller LJ (2002) Refinement of the conformation of a critical region of charge–charge interaction between cholecystokinin and its receptor. Mol Pharmacol 61:1041–1052

    Article  PubMed  CAS  Google Scholar 

  6. Ji Z, Hadac EM, Henne RM, Patel SA, Lybrand TP, Miller LJ (1997) Direct identification of a distinct site of interaction between the carboxyl-terminal residue of cholecystokinin and the type A cholecystokinin receptor using photoaffinity labeling. J Biol Chem 272:24393–24401

    Article  PubMed  CAS  Google Scholar 

  7. Harikumar KG, Pinon DI, Wessels WS, Prendergast FG, Miller LJ (2002) Environment and mobility of a series of fluorescent reporters at the amino terminus of structurally related peptide agonists and antagonists bound to the cholecystokinin receptor. J Biol Chem 277:18552–18560

    Article  PubMed  CAS  Google Scholar 

  8. Harikumar KG, Clain J, Pinon DI, Dong M, Miller LJ (2005) Distinct molecular mechanisms for agonist peptide binding to types A and B cholecystokinin receptors demonstrated using fluorescence spectroscopy. J Biol Chem 280:1044–1050

    Article  PubMed  CAS  Google Scholar 

  9. Hadac EM, Pinon DI, Ji Z, Holicky EL, Henne RM, Lybrand TP, Miller LJ (1998) Direct identification of a second distinct site of contact between cholecystokinin and its receptor. J Biol Chem 273:12988–12993

    Article  PubMed  CAS  Google Scholar 

  10. Ding XQ, Dolu V, Hadac EM, Holicky EL, Pinon DI, Lybrand TP, Miller LJ (2001) Refinement of the structure of the ligand-occupied cholecystokinin receptor using a photolabile amino-terminal probe. J Biol Chem 276:4236–4244

    Article  PubMed  CAS  Google Scholar 

  11. Pearson RK, Miller LJ, Hadac EM, Powers SP (1987) Analysis of the carbohydrate composition of the pancreatic plasmalemmal glycoprotein affinity labeled by short probes for the cholecystokinin receptor. J Biol Chem 262:13850–13856

    PubMed  CAS  Google Scholar 

  12. Hadac EM, Ghanekar DV, Holicky EL, Pinon DI, Dougherty RW, Miller LJ (1996) Relationship between native and recombinant cholecystokinin receptors: role of differential glycosylation. Pancreas 13:130–139

    Article  PubMed  CAS  Google Scholar 

  13. Munson PJ, Rodbard D (1980) Ligand: a versatile computerized approach for characterization of ligand-binding systems. Anal Biochem 107:220–239

    Article  PubMed  CAS  Google Scholar 

  14. Ganguli SC, Park CG, Holtmann MH, Hadac EM, Kenakin TP, Miller LJ (1998) Protean effects of a natural peptide agonist of the G protein-coupled secretin receptor demonstrated by receptor mutagenesis. J Pharmacol Exp Ther 286:593–598

    PubMed  CAS  Google Scholar 

  15. Grynkiewicz G, Poenie M, Tsien RY (1985) A new generation of Ca2+ indicators with greatly improved fluorescence properties. J Biol Chem 260:3440–3450

    PubMed  CAS  Google Scholar 

  16. Beechem JM (1992) Global analysis of biochemical and biophysical data. Methods Enzymol 210:37–54

    Article  PubMed  CAS  Google Scholar 

  17. Harikumar KG, Miller LJ (2002) Applications of fluorescence in the characterization of the ligand-binding domain and activation of the cholecystokinin receptor. Pharmacol Toxicol 91:286–289

    Article  PubMed  CAS  Google Scholar 

  18. Ghanouni P, Gryczynski Z, Steenhuis JJ, Lee TW, Farrens DL, Lakowicz JR, Kobilka BK (2001) Functionally different agonists induce distinct conformations in the G protein coupling domain of the beta 2 adrenergic receptor. J Biol Chem 276:24433–24436

    Article  PubMed  CAS  Google Scholar 

  19. Harikumar KG, Pinon DI, Wessels WS, Dawson ES, Lybrand TP, Prendergast FG, Miller LJ (2004) Measurement of intermolecular distances for the natural agonist peptide docked at the cholecystokinin receptor expressed in situ using fluorescence resonance energy transfer. Mol Pharmacol 65:28–35

    Article  PubMed  CAS  Google Scholar 

  20. Farrens DL, Altenbach C, Yang K, Hubbell WL, Khorana HG (1996) Requirement of rigid-body motion of transmembrane helices for light activation of rhodopsin. Science 274:768–770

    Article  PubMed  CAS  Google Scholar 

  21. Gether U, Kobilka BK (1998) G protein-coupled receptors. II. Mechanism of agonist activation. J Biol Chem 273:17979–17982

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

The authors thank Peter J. Calahan and William S. Wessels for assisting in the biophysical studies, and Eileen Holicky for technical assistance in these studies. We thank Dr. Maoqing Dong for helpful discussions, and Dana Huether for secretarial assistance. This work was supported by National Institutes of Health grant DK32878 and the Fiterman Foundation.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Laurence J. Miller.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Harikumar, K.G., Pinon, D.I. & Miller, L.J. Fluorescence Characteristics of Hydrophobic Partial Agonist Probes of the Cholecystokinin Receptor. Biosci Rep 26, 89–100 (2006). https://doi.org/10.1007/s10540-006-9008-x

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10540-006-9008-x

Keywords

Navigation