Literature DB >> 2432039

[Spectroscopic and thermodynamic investigations on the binding of azure B to chondroitin sulfate and the structure of the metachromatic dye complex].

D Hüglin, W Seiffert, H W Zimmermann.   

Abstract

The binding of azur B to chondroitin sulfate (CHS) was investigated using absorption spectroscopy. In aqueous solutions it is possible to distinguish three different dye species with absorption bands at 646, 597, and 555 nm. They are assigned to monomers, dimers, and higher aggregates of azure B, which become bound to CHS as the dye concentration (CD) increases. The short-wavelength band (555 nm) causes metachromasia in stained histological materials. When saturation occurs, the metachromatic azure B-CHS complex has a 1:1 composition, i.e., each anionic SO-4 and COO(-)-binding site of CHS binds one dye cation. The composition of the saturated metachromatic complex was determined by spectrophotometric and conductometric titration of CHS with azure B, while the SO-4 and COO- content of CHS was determined by conductometric titration of CHS-acid with NaOH. The binding isotherm of azure B to CHS was determined using gelpermeation chromatography. The isotherm can be described by the model of cooperative binding of ligands to linear biopolymers. We found good agreement between theoretical predictions and experimental findings in the range of 0 less than r less than 0.8 (r = the fraction of occupied binding sites). Using a Schwarz plot, we determined the binding constants of nucleation (Kn = 2.5 X 10(3) M-1) and aggregation (Kq = 1.2 X 10(5) M-1), as well as the cooperativity parameter (q = 50), T = 295 K. With increasing CD, the strong cooperativity of the dye binding favors the formation of metachromatic aggregates rather than monomers and dimers. From the temperature dependence of Kq we evaluated the standard binding enthalpy (delta Hoq = -20.0 kJ mol-1) and entropy (delta Soq = 29.7 JK-1 mol-1) of the cooperative dye binding. The binding was found to be strongly exothermic and accompanied by a thermodynamically favorable entropy increase, this being typical of hydrophobic interactions. Solid azure B-CHS complexes were prepared according to a special dialytic technique and were studied using a microspectrophotometer equipped with a polarizer and an analyzer. The metachromatic 1:1 complex has a broad, intense absorption band whose main peak occurs at 560 nm. This corresponds with the maximum of the metachromatic dye complex in aqueous solution, i.e. 555 nm. The CHS chains of the azure B-CHS complex can be mechanically aligned in a preferred direction (k). We were able to prepare excellently orientated and very fine dye-CHS films which were birefringent and dichroic - the more birefringent, the better the mechanical orientation.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1986        PMID: 2432039     DOI: 10.1007/bf00492348

Source DB:  PubMed          Journal:  Histochemistry        ISSN: 0301-5564


  25 in total

1.  THE CONFORMATION OF HYALURONIC ACID AND CHONDROITIN SULFATE C: THE METACHROMATIC REACTION.

Authors:  M D SCHOENBERG; R D MOORE
Journal:  Biochim Biophys Acta       Date:  1964-03-02

2.  The azure dyes: their purification and physicochemical properties. II. Purification of azure B.

Authors:  W Löhr; N Grubhoffer; I Sohmer; D Wittekind
Journal:  Stain Technol       Date:  1975-05

3.  The azure dyes: their purification and physicochemical properties. I. Purification of azure A.

Authors:  W Löhr; I Sohmer; D Wittekind
Journal:  Stain Technol       Date:  1974-11

4.  Aggregation of cationic dyes on acid polysaccharides. I. Spectrophotometric titration with acridine orange and other metachromatic dyes.

Authors:  A L Stone; D F Bradley
Journal:  Biochim Biophys Acta       Date:  1967-10-09

5.  [Romanowsky dyes and romanowsky-Giemsa effect. 1. Azure B, purity and content of dye samples, association (author's transl)].

Authors:  E Zipfel; J R Grezes; W Seiffert; H W Zimmermann
Journal:  Histochemistry       Date:  1981

6.  A standardized Romanowsky stain prepared from purified dyes.

Authors:  P N Marshall; S A Bentley; S M Lewis
Journal:  J Clin Pathol       Date:  1975-11       Impact factor: 3.411

7.  Batch variations in commercial dyes employed for Romanowsky-type staining: a thin-layer chromatographic study.

Authors:  P N Marshall; S M Lewis
Journal:  Stain Technol       Date:  1974-11

8.  An evaluation of some commerical Romanowsky stains.

Authors:  P N Marshall; S A Bentley; S M Lewis
Journal:  J Clin Pathol       Date:  1975-08       Impact factor: 3.411

9.  Fractionation of proteoglycans from bovine corneal stroma.

Authors:  I Axelsson; D Heinegård
Journal:  Biochem J       Date:  1975-03       Impact factor: 3.857

10.  Details of glycosaminoglycan conformations and intermolecular interactions.

Authors:  S Arnott; W T Winter
Journal:  Fed Proc       Date:  1977-01
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  5 in total

Review 1.  Standardization of reagents and methods used in cytological and histological practice with emphasis on dyes, stains and chromogenic reagents.

Authors:  H O Lyon; A P De Leenheer; R W Horobin; W E Lambert; E K Schulte; B Van Liedekerke; D H Wittekind
Journal:  Histochem J       Date:  1994-07

2.  [Romanowsky dyes and the Romanowsky-Giemsa effect. 4. Binding of azure B to DNA].

Authors:  R Müller-Walz; H W Zimmermann
Journal:  Histochemistry       Date:  1987

3.  Romanowsky dyes and Romanowsky-Giemsa effect. 5. Structural investigations of the purple DNA-AB-EY dye complexes of Romanowsky-Giemsa staining.

Authors:  K Friedrich; W Seiffert; H W Zimmermann
Journal:  Histochemistry       Date:  1990

4.  Experimental mucopolysaccharidosis: preservation and ultrastructural visualization of intralysosomal glycosaminoglycans by use of the cationic dyes cuprolinic blue and toluidine blue.

Authors:  R Lüllmann-Rauch
Journal:  Histochemistry       Date:  1989

5.  [Model investigations on the structure of the purple dye complex of Giemsa staining].

Authors:  K Friedrich; D Hüglin; W Seiffert; H W Zimmermann
Journal:  Histochemistry       Date:  1989
  5 in total

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