Literature DB >> 3816697

Fluorescence of 3-keto-steroids in aqueous solution. Probes for steroid-protein interactions.

M Kempfle, R Müller, R Palluk, K A Zachariasse.   

Abstract

The physiologically important 3-keto-steroids are non-fluorescent or only weakly fluorescent in protic as well as in aprotic solvents. In contrast, the 4,6,8(14)-triene-3-one steroids are highly fluorescent in aqueous solution but they do not appreciably fluoresce in other solvents. Evidence is presented that the introduction of double bonds into the skeleton of the 3-keto-steroids leads to a decrease of the energy of the lowest pi-pi* state, bringing this level into the neighbourhood of the non-fluorescent n-pi* state. As a consequence, for two states of approximately the same energy, relatively small perturbations such as those due to solvent interactions, protein binding and micelle formation, will then determine whether a system will fluoresce (pi-pi* state lowest) or not (n-pi* state lowest). When the fluorescent 3-keto-steroids, having three conjugated double bonds, bind to proteins, the fluorescence intensity becomes almost zero, making these compounds useful as probes for steroid-protein interactions. This quenching of the fluorescence is explained by a decrease in energy of the n-pi* state relative to the pi-pi* state of th steroids due to hydrophobic interactions with the proteins.

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Year:  1986        PMID: 3816697     DOI: 10.1007/bf00260400

Source DB:  PubMed          Journal:  Eur Biophys J        ISSN: 0175-7571            Impact factor:   1.733


  4 in total

1.  Kinetic studies in bile acid micelles.

Authors:  M Chen; M Grätzel; J K Thomas
Journal:  J Am Chem Soc       Date:  1975-04-16       Impact factor: 15.419

Review 2.  Fluorescent sterols: probe molecules of membrane structure and function.

Authors:  F Schroeder
Journal:  Prog Lipid Res       Date:  1984       Impact factor: 16.195

Review 3.  [Binding of progesterone and other steroid hormones to serum proteins: 3d Adolf Butenandt lecture].

Authors:  U Westphal
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1978-04

4.  Biosynthesis of ergosta-4,6,8(14),22-tetraen-3-one. In vivo incorporation of a 1,4-dioxide.

Authors:  J D White; S I Taylor
Journal:  J Am Chem Soc       Date:  1970-09-23       Impact factor: 15.419

  4 in total

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