Literature DB >> 2307143

Binding of Cu(II), Tb(III) and Fe(III) to chicken ovotransferrin. A kinetic study.

T Taniguchi1, K Ichimura, S Kawashima, T Yamamura, Y Tachi'iri, K Satake, H Kihara.   

Abstract

The kinetics of binding of Cu(II), Tb(III) and Fe(III) to ovotransferrin have been investigated using the stopped-flow technique. Rate constants for the second-order reaction, k+, were determined by monitoring the absorbance change upon formation of the metal-transferrin complex in time range of milliseconds to seconds. The N and C sites appeared to bind a particular metal ion with the same rate; thus, average formation rate constants k+ (average) were 2.4 x 10(4) M-1 s-1 and 8.3 x 10(4) M-1 s-1 for Cu(II) and Tb(III) respectively. Site preference (N site for Cu(II) and C site for Tb(III] is then mainly due to the difference in dissociation rate constant for the metals. Fe(III) binding from Fe-nitrilotriacetate complex to apo-ovotransferrin was found to be more rapid, giving an average formation rate constant k+ (average) of 5 x 10(5) M-1 s-1, which was followed by a slow increase in absorbance at 465 nm. This slow process has an apparent rate constant in the range 3 s-1 to 0.5 s-1, depending upon the degree of Fe(III) saturation. The variation in the rate of the second phase is thought to reflect the difference in the rate of a conformational change for monoferric and diferric ovotransferrins. Monoferric ovotransferrin changes its conformation more rapidly (3.4 s-1) than diferric ovotransferrin (0.52 s-1). A further absorbance decrease was observed over a period of several minutes; this could be assigned to release of NTA from the complex, as suggested by Honda et al. (1980).

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Year:  1990        PMID: 2307143     DOI: 10.1007/bf00185414

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


  19 in total

1.  THE SPECIFIC BINDING OF IRON(III) AND COPPER(II) TO TRANSFERRIN AND CONALBUMIN.

Authors:  R AASA; B G MALMSTROEM; P SALTMAN
Journal:  Biochim Biophys Acta       Date:  1963-09-24

2.  The denaturation of proteins. IV. Conalbumin and iron(III)-conalbumin in urea solution.

Authors:  A N GLAZER; H A McKENZIE
Journal:  Biochim Biophys Acta       Date:  1963-04-02

3.  Study of the nature of the metal-binding sites and estimate of the distance between the metal-binding sites in transferrin using trivalent lanthanide ions as fluorescent probes.

Authors:  C Ka Luk
Journal:  Biochemistry       Date:  1971-07-20       Impact factor: 3.162

4.  Ultraviolet difference spectrl studies of conalbumin complexes with transition metal ions.

Authors:  A T Tan; R C Woodworth
Journal:  Biochemistry       Date:  1969-09       Impact factor: 3.162

5.  The primary structure of hen ovotransferrin.

Authors:  J Williams; T C Elleman; I B Kingston; A G Wilkins; K A Kuhn
Journal:  Eur J Biochem       Date:  1982-02

6.  Evidence for the bilobal nature of diferric rabbit plasma transferrin.

Authors:  B Gorinsky; C Horsburgh; P F Lindley; D S Moss; M Parkar; J L Watson
Journal:  Nature       Date:  1979-09-13       Impact factor: 49.962

7.  Human transferrin: cDNA characterization and chromosomal localization.

Authors:  F Yang; J B Lum; J R McGill; C M Moore; S L Naylor; P H van Bragt; W D Baldwin; B H Bowman
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

8.  Facilitation of Fe(II) autoxidation by Fe(3) complexing agents.

Authors:  D C Harris; P Aisen
Journal:  Biochim Biophys Acta       Date:  1973-11-02

9.  Negative cooperativity of chicken ovotransferrin on Al(III)-binding.

Authors:  K Ichimura; H Kihara; T Yamamura; K Satake
Journal:  J Biochem       Date:  1989-07       Impact factor: 3.387

10.  The kinetics and mechanism of iron(3) exchange between chelates and transferrin. IV. The reaction of transferrin with iron(3) nitrilotriacetate.

Authors:  G W Bates; J Wernicke
Journal:  J Biol Chem       Date:  1971-06-10       Impact factor: 5.157

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  3 in total

1.  Heat-induced superaggregation of amphotericin B reduces its in vitro toxicity: a new way to improve its therapeutic index.

Authors:  F Gaboriau; M Chéron; C Petit; J Bolard
Journal:  Antimicrob Agents Chemother       Date:  1997-11       Impact factor: 5.191

2.  The removal of a disulfide bridge in CotA-laccase changes the slower motion dynamics involved in copper binding but has no effect on the thermodynamic stability.

Authors:  André T Fernandes; Manuela M Pereira; Catarina S Silva; Peter F Lindley; Isabel Bento; Eduardo Pinho Melo; Lígia O Martins
Journal:  J Biol Inorg Chem       Date:  2011-03-03       Impact factor: 3.358

3.  Effects of aggregation and solvent on the toxicity of amphotericin B to human erythrocytes.

Authors:  P Legrand; E A Romero; B E Cohen; J Bolard
Journal:  Antimicrob Agents Chemother       Date:  1992-11       Impact factor: 5.191

  3 in total

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