Skip to main content
Log in

Purification and characterization of the carboxyl-domain of human hexokinase type III expressed as fusion protein

  • Published:
Molecular and Cellular Biochemistry Aims and scope Submit manuscript

Abstract

In mammalian tissues hexokinase (ATP:D-hexose 6-phosphotransferase, EC 2.7.1.1) exists as four isoenzymes encoded by distinct genes. These proteins are homologous and are organized in two homologous domains, with the exception of hexokinase type IV which has only one. This organization is believed to be the result of a duplication and tandem fusion event involving the gene encoding for the ancestral hexokinase. In this study we cloned the carboxyl-domain of human hexokinase type III and expressed it in Escherichia coli as a glutathione S-transferase fusion protein, using the pGEX-2T expression vector. The recombinant protein showed catalytic activity. A comparative study of the kinetic properties of the expressed carboxyl-domain and the enzyme partially purified from human lymphocytes is also shown. The results now allow a better understanding of the role of the carboxyl-domain in determining the catalytic properties of the enzyme.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

SSPE:

0.15 mol/l NaCl/ 10 mmol/l Na-phosphate/ 1 mmol/l EDTA pH 7.4

Denhardt's:

0.02 g/l BSA Fractions V/ 0.02 g/l Ficoll 400/ 0.02 g/l polyvinylpyrollidone

SSC:

0.15 mol/l NaCl/ 15 mmol/l Na3-citrate pH 7.0

IPTG:

isopropyl β-D-thiogalactopyranoside

PMSF:

phenylmethylsulfonyl fluoride

Glc-6-P:

glucose 6-phosphate

PAGE:

polyacrylamide gel electrophoresis

References

  1. Wilson JE: Regulation of mammalian hexokinase activity. In E. Beitner (ed.). Regulation of Carbohydrate Metabolism. CRC Press, Boca Raton, FL, 1984, vol I, pp 45–85

    Google Scholar 

  2. Schwab DA, Wilson JE: The complete amino acid sequence of the catalytic domain of rat brain hexokinase, deduced from the cloned cDNA. J Biol Chem 263: 3220–3224, 1988

    Google Scholar 

  3. Nishi S, Seino S, Bell GI: Human hexokinase: sequence of amino- and carboxyl-terminal halves are homologous. Biochem Biophys Res Commun 157: 937–943, 1988

    Google Scholar 

  4. Andreone TL, Printz RL, Pilkis SJ, Magnuson MA, Granner DK: The amino acid sequence of rat liver glucokinase deduced from cloned cDNA. J Biol Chem 264: 363–369, 1989

    Google Scholar 

  5. Schwab DA, Wilson JE: Complete amino acid sequence of rat brain hexokinase, deduced from the cloned cDNA, and proposed structure of a mammalian hexokinase. Proc Natl Acad Sci USA 86: 2563–2567, 1989

    Google Scholar 

  6. Arora KK, Fanciulli M, Pedersen L: Glucose phosphorylation in tumor cells. Cloning, sequencing, and overexpression in active form of a fulllength cDNA enconding a mitochondrial bindable form of hexokinase. J Biol Chem 265: 6481–6488, 1990

    Google Scholar 

  7. Schwab DA, Wilson JE: Complete amino acid sequence of the type III isozyme of rat hexokinase, deduced from the cloned cDNA. Arch Biochem Biophys 285: 365–370, 1991

    Google Scholar 

  8. Thelen AP, Wilson JE: Complete amino acid sequence of the type II isozyme of rat hexokinase, deduced from the cloned cDNA: comparison with a hexokinase from Novikoff ascite tumor. Arch Biochem Biophys 286: 645–651, 1991

    Google Scholar 

  9. Deeb SS, Malkki M, Laakso M: Human hexokinase II: sequence and homology to other hexokinases. Biochem Biophys Res Commun 197: 98–74, 1993

    Google Scholar 

  10. Schirch DM, Wilson JE: Rat brain hexokinase: location of the substrate hexose binding site in a structural domain at the C-terminus of the enzyme. Arch Biochem Biophys 254: 385–396, 1987

    Google Scholar 

  11. White TK, Wilson JE: Rat brain hexokinase: location of the allosteric regulatory site in a structural domain at the N-termnous of the enzyme. Arch Biochem Biophys 259: 402–411, 1987

    Google Scholar 

  12. White TK, Wilson JE: Isolation and characterization of the discrete N- and C-terminal halves of rat brain hexokinase: retention of full catalytic activity in the isolated C-terminal half. Arch Biochem Biophys 274: 375–393, 1989

    Google Scholar 

  13. Arora KK, Filburn CR, Pedersen PL: Structure/function relationships in hexokinase. Site directed mutational analyses and characterization of overexpressed fagments implicate different functions for the N- and C-terminal halves of the enzyme. J Biol Chem 268: 18259–18266, 1993

    Google Scholar 

  14. Heumann S, Falkenbcrg F, Pfleiderer G: Purification and immunological characterization of the human hexokinase isoenzymes I and III (ATP-D-hexose 6-phosphotranferase EC 2.7.1.1). 334: 328–342, 1974

    Google Scholar 

  15. Stocchi V, Magnani M, Novelli G, Dacha M, Fornaini G: Pig red blood cell hexokinase: evidence for the presence of hexokinase types II and III, and their purification and characterization. Arch Biochem Biophys 226: 365–376, 1983

    Google Scholar 

  16. Radojkovic J, Ureta T: Hexokinase isoenzymes from the Novikoff hepatoma. Purification, kinetic and structural characterization, with emphasis on hexokinase C. Biochem J 242: 895–903, 1987

    Google Scholar 

  17. Magnani M, Stocchi V, Serafini N, Piatti E, Dacha M, Fornaini G: Pig red blood cell hexokinase: regulatory characteristics and possible physiological role. Arch Biochem Biophys 226: 377–387, 1983

    Google Scholar 

  18. Stocchi V, Masat L, Biagiarelli B, Piccoli G, Palma F, Cucchiarini L, Dacha M: Preparative purification of pig red blood cell hexokinase type III using a new efficient chromatographic support. Prep Biochem 22: 41–51, 1992

    Google Scholar 

  19. Preller A, Wilson JE: Localization of the type III isozyme of hexokinase at the nuclear periphery. Arch Biochem Biophys 294: 482–492, 1992

    Google Scholar 

  20. Maniatis T, Fritsch EF, Sambrook J: Chris Noland: Molecular Cloning, a Laboratory Manual. Cold Spring, Harbor, NY, 2nd edition, 1989

  21. Sanger F, Coulson AR, Barrel BG, Smith AJH, Roe BA: Cloning in single-stranded bacteriophage as an aid to rapid DNA sequencing. J Mol Biol 143: 161–178, 1980

    Google Scholar 

  22. Smith DB, Johnson KS: Single-step purification of polypeptides expressed inEsherichia coli as fusions with glutathione S-transferase. Gene 67: 31–40, 1988

    Google Scholar 

  23. Vandenbroeck K, Martens E, D'Andrea S, Billiau A: Refolding an single-step purification of porcine interferon-y fromEscherichia coli inclusion bodies. E J Biochem 215: 481–486, 1993

    Google Scholar 

  24. Stocchi V, Masat L, Biagiarelli B, Accorsi A, Piccoli G, Palma F, Cucchiarini L, Dacha M: High resolutions of multiple forms of red blood cell enzymes using a Toyopearl DEAE 650 S. Prep Biochem 22: 11–40, 1992

    Google Scholar 

  25. Frangioni JV, Benjamin GN: Solubilization and purification of enzymatically active glutathione S-transferare (pGEX) fusion protein. Anal Biochem 210: 179–187, 1993

    Google Scholar 

  26. Guan KL, Dixon JE: Eukaryotic proteins expressed inEscherichia coli: an improved thrombin cleavage and purification procedure of fusion proteins with glutathione S-transferase. Anal Biochem 192: 262–267, 1991

    Google Scholar 

  27. Magnani M, Bianchi M, Casabianca A, Stocchi V, Daniele A, Altruda F, Ferrone M, Silengo L: A recombinant human ‘mini’-hexokinase is catalytically active and regulate by hexose 6-phosphates. Biochem J 285: 193–199, 1992

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Palma, F., Agostini, D., Mason, P. et al. Purification and characterization of the carboxyl-domain of human hexokinase type III expressed as fusion protein. Mol Cell Biochem 155, 23–29 (1996). https://doi.org/10.1007/BF00714329

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00714329

Key words

Navigation