Specificity of receptor-ligand interactions and their effect on dimerisation as observed by electrospray mass spectrometry: bile acids form stable adducts to the RXRα

• Published in: Journal of mass spectrometry. Vol. 40; no. 11; pp. 1448 - 1461
• Main Authors: Lengqvist, Johan, Mata de Urquiza, Alexander, Perlmann, Thomas, Sjövall, Jan, Griffiths, William J.
• Format: Journal Article
• Language: English
• Published: Chichester, UK John Wiley & Sons, Ltd 01.11.2005; Wiley
• Subjects: bile acids; Biological and medical sciences; Cell receptors; Cell structures and functions; electrospray ionization mass spectrometry; Fundamental and applied biological sciences. Psychology; lipids; Miscellaneous; Molecular and cellular biology; non-covalent complexes; nuclear receptor; Steroid; Stoichiometry; Agonist; Nuclear receptor; lipids; Ligand; Molecular interaction; Docosahexaenoic acid; Electrospray; bile acids; Bile acid; Dimerization; Molecular adduct; Ligand binding; Non covalent bond; electrospray ionization mass spectrometry; Stability; non-covalent complexes; RXRα retinoid receptor; Biological fixation; Analysis method; Medium effect; Affinity; Gas phase; Mass spectrometry
• ISSN: 1076-5174; 1096-9888
• DOI: 10.1002/jms.925

Electrospray (ES) mass spectrometry data is presented showing that agonist binding to the nuclear receptor (NR), retinoid X receptor α (RXRα), is competitive. The competitive nature of agonist binding can be used to discriminate between the specific and non‐specific binding of small lipophilic molecules to NRs. Further, data is presented which show that high‐affinity ligand binding to the RXRα ligand‐binding domain (LBD) stabilises the domain homodimer. The results indicate that homodimerisation, a functional property of the receptor associated with the binding of agonist ligands, could be used to discriminate between specific and non‐specific binding events. Additionally, we report on the remarkable stability of the gas‐phase complex between the RXRα LBD protein and endogenous bile acids. Protein–bile acid interactions in the gas phase were found to be surprisingly strong, withstanding ‘in‐source’ fragmentation in the ES interface, and, in the case of taurocholic acid (TCA) and lithocholic acid‐3‐sulphate (LCA‐3‐sulphate), collision‐induced dissociation within the collision cell of a tandem mass spectrometer. Bile acids were found to be inactive towards RXRα in transfection assays, and have not been reported to be ligands for the RXRα, although lithocholic acid (LCA) has been found to be a competitor in the photoaffinity labelling of RXRβ with 9‐cis‐retinoic acid (9‐cis‐RA). The observation of strong RXRα‐bile acid non‐covalent complexes in ES mass spectrometry highlight the danger of extrapolating gas‐phase binding data to the solution phase and further to a possible biological activity, particularly when surface‐active compounds such as bile acids are involved. The introduction of a competitive ligand‐binding experiment can alleviate this problem and allow the differentiation between specific and non‐specific binding. Copyright © 2005 John Wiley & Sons, Ltd.