Literature DB >> 446878

Competitive binding studies with glucocorticoid receptors from rat-thymus cells: differential temperature-dependence of steroid binding.

T R Jones, J C Sloman, P A Bell.   

Abstract

Competitive steroid-binding studies were performed with intact rat thymus cells and with cytosol preparations at different temperatures using [1,2-3H]dexamethasone as the labelled ligand. Steroids lacking a 17 alpha-hydroxyl group, such as corticosterone, were better able to compete with [1,2-3H]dexamethasone for binding to glucocorticoid receptors at 0 degrees C than compounds containing a 17 alpha-hydroxyl substituent, such as cortisol. At 37 degrees C the reverse was true. This temperature-dependent change in relative affinities appeared to be unrelated to steroid metabolism or receptor activation, and to depend only on the thermodynamic parameters of the steroid--receptor interaction. Relative biological activities for different steroids agree more closely with the relative affinities determined at 37 degrees C than with those determined at lower temperatures.

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Year:  1979        PMID: 446878     DOI: 10.1016/0303-7207(79)90078-9

Source DB:  PubMed          Journal:  Mol Cell Endocrinol        ISSN: 0303-7207            Impact factor:   4.102


  3 in total

1.  Thermodynamics of steroid binding to the human glucocorticoid receptor.

Authors:  P H Eliard; G G Rousseau
Journal:  Biochem J       Date:  1984-03-01       Impact factor: 3.857

2.  Glucocorticoid--receptor interactions. Studies of the negative co-operativity induced by steroid interactions with a secondary, hydrophobic, binding site.

Authors:  T R Jones; P A Bell
Journal:  Biochem J       Date:  1980-04-15       Impact factor: 3.857

3.  Glucocorticoid-receptor interactions. Discrimination between glucocorticoid agonists and antagonists by means of receptor-binding kinetics.

Authors:  T R Jones; P A Bell
Journal:  Biochem J       Date:  1982-06-15       Impact factor: 3.857

  3 in total

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