Literature DB >> 3193403

Apparent competitive inhibition of radioligand binding to receptors: experimental and theoretical considerations in the analysis of equilibrium binding data.

G Tomlinson1, M R Hnatowich.   

Abstract

Radioligand binding and displacement experiments are often interpreted in terms of simple competition between two ligands for occupancy of a single binding site on a receptor. Given our current understanding of the complexities of receptor structure and function, it is probable that more complex interactions occur in many cases. By analysis of a hypothetical two-site receptor model, we show that apparent competitive inhibition can arise in several ways, depending on the specificities of the two sites and the interactions between them. We show that binding experiments can in some cases be used to rule out certain models from among a group of apparently plausible ones, provided that experimental criteria are met which permit a meaningful statistical comparison of models to be made. Ideally, these should include: i) an independent study of ligand and inhibitor binding in the absence of each other; ii) carrying out saturation binding and displacement experiments over as wide a range of ligand and inhibitor concentrations as possible; iii) computerized curve-fitting and statistical analysis as a tool for model-testing. While practical limitations may restrict the attainment of such goals, a thorough study of the equilibrium binding properties of a particular receptor system provides the foundation for the design of more definitive experiments at the molecular level, upon which the proof of any binding model ultimately must rest.

Mesh:

Year:  1988        PMID: 3193403     DOI: 10.3109/10799898809049027

Source DB:  PubMed          Journal:  J Recept Res        ISSN: 0197-5110


  6 in total

1.  Experimental design and estimation of parameters in complex radioligand binding systems.

Authors:  C M Staschen; L D Homer
Journal:  J Pharmacokinet Biopharm       Date:  1996-12

2.  Differential recognition of snake venom proteins expressing specific Arg-Gly-Asp (RGD) sequence motifs by wild-type and variant integrin alphaIIbbeta3: further evidence for distinct sites of RGD ligand recognition exhibiting negative allostery.

Authors:  S Rahman; G Flynn; A Aitken; Y Patel; F Hussain; X Lu; J C Loftus; D French; E Wijelath; K Strand; G F Savidge
Journal:  Biochem J       Date:  2000-02-01       Impact factor: 3.857

3.  The integrin alpha IIb beta 3 contains distinct and interacting binding sites for snake-venom RGD (Arg-Gly-Asp) proteins. Evidence that the receptor-binding characteristics of snake-venom RGD proteins are related to the amino acid environment flanking the sequence RGD.

Authors:  S Rahman; X Lu; V V Kakkar; K S Authi
Journal:  Biochem J       Date:  1995-11-15       Impact factor: 3.857

4.  Reovirus type 3 binds to antagonist domains of the beta-adrenergic receptor.

Authors:  S T Donta; J D Shanley
Journal:  J Virol       Date:  1990-02       Impact factor: 5.103

5.  Regulation of human D(1), d(2(long)), d(2(short)), D(3) and D(4) dopamine receptors by amiloride and amiloride analogues.

Authors:  S R Hoare; M C Coldwell; D Armstrong; P G Strange
Journal:  Br J Pharmacol       Date:  2000-07       Impact factor: 8.739

6.  Divalent cation competition with [3H]saxitoxin binding to tetrodotoxin-resistant and -sensitive sodium channels. A two-site structural model of ion/toxin interaction.

Authors:  D D Doyle; Y Guo; S L Lustig; J Satin; R B Rogart; H A Fozzard
Journal:  J Gen Physiol       Date:  1993-02       Impact factor: 4.086

  6 in total

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