Literature DB >> 942376

Formation of monoferric ovotransferrins in the presence of chelates.

J W Donovan, R A Beardslee, K D Ross.   

Abstract

1. When ovotransferrin is partially saturated with iron, endotherms for apo-ovotransferrin, two monoferric ovotransferrins and Fe2-ovotransferrin are observed by differential scanning calorimetry. The relative sizes of the endotherms are changed in the presence of the iron-chelating agents nitrilotriacetic acid and ATP. 2. When iron is added as Fe(III)-nitrilotriacetate, at Fe-nitrilotriacetate: ovotransferrin ratios less than unity, the endotherm for Fe2-ovotransferrin is essentially absent. At Fe-nitrilotriacetate: ovotransferrin ratios of unity the only species present in solution in appreciable concentration as evidenced by their differential-scanning-calorimetry endotherms, are two monoferric ovotransferrins in approximately equal amounts. At Fe-nitrilotriacetate: ovotransferrin ratios greater than unity, the apo-ovotransferrin endotherm is absent, and the endotherms for the two monoferric ovotransferrins decrease in size as the endotherm for Fe2-ovotransferrin increases. 3. In the presence of nitrilotriacetate, binding of iron to the two sites of ovotransferrin is highly anti-co-operative, but essentially indiscriminate. When monoferric ovotransferrin is formed from apo-ovotransferrin, binding at one site is slightly favoured compared with binding at the other site, but once iron has been bound at either site, the binding affinity for iron at the unoccupied site is much decreased.

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Year:  1976        PMID: 942376      PMCID: PMC1172632          DOI: 10.1042/bj1530631

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  28 in total

1.  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

2.  Difference between the two iron-binding sites of transferrin.

Authors:  J V Princiotto; E J Zapolski
Journal:  Nature       Date:  1975-05-01       Impact factor: 49.962

3.  Half-of-the sites reactivity and negative co-operativity: the case of yeast glyceraldehyde 3-phosphate dehydrogenase.

Authors:  W B Stallcup; D E Koshland
Journal:  J Mol Biol       Date:  1973-10-15       Impact factor: 5.469

Review 4.  Half-site reactivity.

Authors:  F Seydoux; O P Malhotra; S A Bernhard
Journal:  CRC Crit Rev Biochem       Date:  1974-03

5.  A thermodynamic approach to the problem of stabilization of globular protein structure: a calorimetric study.

Authors:  P L Privalov; N N Khechinashvili
Journal:  J Mol Biol       Date:  1974-07-05       Impact factor: 5.469

6.  Thermal transitions of proteins.

Authors:  H B Bull; K Breese
Journal:  Arch Biochem Biophys       Date:  1973-06       Impact factor: 4.013

7.  Spectroscopic evidence for a difference between the iron-binding sites of conalbumin.

Authors:  P Aisen; G Lang; R C Woodworth
Journal:  J Biol Chem       Date:  1973-01-25       Impact factor: 5.157

8.  Bicarbonate and the binding of iron to transferrin.

Authors:  P Aisen; R Aasa; B G Malmström; T Vänngård
Journal:  J Biol Chem       Date:  1967-05-25       Impact factor: 5.157

9.  The formation of iron-binding fragments of hen ovotransferrin by limited proteolysis.

Authors:  J Williams
Journal:  Biochem J       Date:  1974-09       Impact factor: 3.857

10.  COMPOUNDS OF FERRIC IRON WITH ADENOSINE TRIPHOSPHATE AND OTHER NUCLEOSIDE PHOSPHATES.

Authors:  C R GOUCHER; J F TAYLOR
Journal:  J Biol Chem       Date:  1964-07       Impact factor: 5.157

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  1 in total

1.  The iron-binding properties of hen ovotransferrin.

Authors:  J Williams; R W Evans; K Moreton
Journal:  Biochem J       Date:  1978-08-01       Impact factor: 3.857

  1 in total

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