Literature DB >> 10981810

Reactivation and refolding of reassociated dimers of rabbit muscle creatine kinase.

Y D Park1, K Huang, H M Zhou.   

Abstract

Creatine kinase (ATP:creatine N-phosphotransferase, EC 2.7.3.2) is a good model for studying dissociation and reassociation during unfolding and refolding. This study compares self-reassociated CK dimers and CK dimers that contain hybrid dimers under proper conditions. Creatine kinase forms a monomer when denatured in 6 M urea for 1 h which will very quickly form a dimer when the denaturant is diluted under suitable conditions. After modification by DTNB, CK was denatured in 6 M urea to form a modified CK monomer. Dimerization of this modified subunit of CK occurred upon dilution into a suitable buffer containing DTT. Therefore, three different types of reassociated CK dimers including a hybrid dimer can be made from two different CK monomers in the proper conditions. The CK monomers are from a urea-denatured monomer of DTNB-modified CK and from an unmodified urea dissociated monomer. Equal enzyme concentration ratios of these two monomers were mixed in the presence of urea, then diluted into the proper buffer to form the three types of reassociated CK dimers including the hybrid dimer. Reassociated CK dimers including all three different types recover about 75% activity following a two-phase course (k1 = 4.88 x 10(-3) s(-1), k2 = 0.68 x 10(-3) s(-1)). Intrinsic fluorescence spectra of the three different CK monomers which were dissociated in 6 M urea, dissociated in 6 M urea after DTNB modification, and a mixture of the first two dissociated enzymes were studied in the presence of the denaturant urea. The three monomers had different fluorescence intensities and emission maxima. The intrinsic fluorescence maximum intensity changes of the reassociated CK dimers were also studied. The refolding processes also follow biphasic kinetics (k1 = 3.28 x 10(-)3 s(-1), k2 = 0.11 x 10(-3) S(-1)) after dilution in the proper solutions. Tsou's method [Tsou (1988), Adv. Enzymol. Rel. Areas Mol. Biol. 61, 381-436] was also used to measure the kinetic reactivation rate constants for the different three types of reassociated CK dimers, with different kinetic reactivation rate constants observed for each type. CK dissociation and reassociation schemes are suggested based on the results.

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Year:  2000        PMID: 10981810     DOI: 10.1023/a:1007051619017

Source DB:  PubMed          Journal:  J Protein Chem        ISSN: 0277-8033


  24 in total

1.  Reactivation and refolding of a partially folded creatine kinase modified by 5,5'-dithio-bis(2-nitrobenzoic acid).

Authors:  Y Yang; Y D Park; T W Yu; H M Zhou
Journal:  Biochem Biophys Res Commun       Date:  1999-06-07       Impact factor: 3.575

2.  Is the subunit the minimal function unit of creatine kinase?

Authors:  X C Wang; H M Zhou; Z X Wang; C L Tsou
Journal:  Biochim Biophys Acta       Date:  1990-07-06

3.  The presence of reactive SH groups in the enzymatically active dicyano derivative of creatine kinase.

Authors:  H M Zhou; C L Tsou
Journal:  Biochim Biophys Acta       Date:  1987-01-30

4.  Comparison of activity and conformation changes during refolding of urea-denatured creatine kinase.

Authors:  H M Zhou; C L Tsou
Journal:  Biochim Biophys Acta       Date:  1986-01-17

Review 5.  Kinetics of substrate reaction during irreversible modification of enzyme activity.

Authors:  C L Tsou
Journal:  Adv Enzymol Relat Areas Mol Biol       Date:  1988

6.  Comparison of the rates of inactivation and conformational changes of creatine kinase during urea denaturation.

Authors:  Q Z Yao; M Tian; C L Tsou
Journal:  Biochemistry       Date:  1984-06-05       Impact factor: 3.162

7.  Changes in circular dichroism and exposure of buried thiol groups during denaturation of rabbit muscle creatine kinase.

Authors:  Q Z Yao; S J Liang; M Tian; C L Zou
Journal:  Sci Sin B       Date:  1985-05

8.  Studies on adenosine triphosphate transphophorylases. V. Studies on the polypeptide chains of the crystalline adenosine triphosphate-creatine transphosphorylase from rabbit skeletal muscle.

Authors:  R H Yue; R H Palmieri; O E Olson; S A Kuby
Journal:  Biochemistry       Date:  1967-10       Impact factor: 3.162

9.  The comparative enzymology of creatine kinases. II. Physical and chemical properties.

Authors:  D M Dawson; H M Eppenberger; N O Kaplan
Journal:  J Biol Chem       Date:  1967-01-25       Impact factor: 5.157

10.  Rabbit muscle creatine phosphokinase. CDNA cloning, primary structure and detection of human homologues.

Authors:  S Putney; W Herlihy; N Royal; H Pang; H V Aposhian; L Pickering; R Belagaje; K Biemann; D Page; S Kuby
Journal:  J Biol Chem       Date:  1984-12-10       Impact factor: 5.157

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  1 in total

1.  Reactivation kinetics of guanidine hydrochloride-denatured creatine kinase measured using the substrate reaction.

Authors:  Y D Park; Z F Cao; H M Zhou
Journal:  J Protein Chem       Date:  2001-01
  1 in total

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