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Research ArticleArticle

Selective Abolishment of Pyrimidine Nucleoside Kinase Activity of Herpes Simplex Virus Type 1 Thymidine Kinase by Mutation of Alanine-167 to Tyrosine

Bart Degrève, Robert Esnouf, Erik De Clercq and Jan Balzarini
Molecular Pharmacology December 2000, 58 (6) 1326-1332; DOI: https://doi.org/10.1124/mol.58.6.1326
Bart Degrève
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Robert Esnouf
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Erik De Clercq
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Jan Balzarini
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Abstract

Herpes simplex virus type 1 (HSV-1) encodes a thymidine kinase (TK) that markedly differs from mammalian nucleoside kinases in terms of substrate specificity. It recognizes both pyrimidine 2′-deoxynucleosides and a variety of purine nucleoside analogs. Based on a computer modeling study and in an attempt to modify this specificity, an HSV-1 TK mutant enzyme containing an alanine-to-tyrosine mutation at amino acid position 167 was constructed. Compared with wild-type HSV-1 TK, the purified mutant HSV-1 TK(A167Y) enzyme was heavily compromised in phosphorylating pyrimidine nucleosides such as (E)-5-(2-bromovinyl)-2′-deoxyuridine and the natural substrate dThd, whereas its ability to phosphorylate the purine nucleoside analogs ganciclovir (GCV) and lobucavir was only reduced ∼2-fold. Moreover, a markedly decreased competition of natural pyrimidine nucleosides (i.e., thymidine) with purine nucleoside analogs for phosphorylation by HSV-1 TK(A167Y) was observed. Human osteosarcoma cells transduced with the wild-type HSV-1 TK gene were extremely sensitive to the cytostatic effects of antiherpetic pyrimidine [i.e., (E)-5-(2-bromovinyl)-2′-deoxyuridine] and purine (i.e., GCV) nucleoside analogs. Transduction with the HSV-1 TK(A167Y) gene sensitized the osteosarcoma cells to a variety of purine nucleoside analogs, whereas there was no measurable cytostatic activity of pyrimidine nucleoside analogs. The unique properties of the A167Y mutant HSV-1 TK may give this enzyme a therapeutic advantage in an in vivo setting due to the markedly reduced dThd competition with GCV for phosphorylation by the HSV-1 TK.

Footnotes

    • Received June 12, 2000.
    • Accepted September 7, 2000.
  • Send reprint requests to: Jan Balzarini, Rega Institute for Medical Research, Katholieke Universiteit Leuven, Minderbroedersstraat 10, B-3000 Leuven, Belgium. E-mail:jan.balzarini{at}rega.kuleuven.ac.be

  • This work was supported by Project 00/12 from the Flemish “Geconcerteerde Onderzoeksacties,” and the “Belgische Federatie tegen kanker.” Bart Degrève is the recipient of a fellowship from the “Belgische Federatie tegen kanker.”

  • The American Society for Pharmacology and Experimental Therapeutics
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Molecular Pharmacology: 58 (6)
Molecular Pharmacology
Vol. 58, Issue 6
1 Dec 2000
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Research ArticleArticle

Selective Abolishment of Pyrimidine Nucleoside Kinase Activity of Herpes Simplex Virus Type 1 Thymidine Kinase by Mutation of Alanine-167 to Tyrosine

Bart Degrève, Robert Esnouf, Erik De Clercq and Jan Balzarini
Molecular Pharmacology December 1, 2000, 58 (6) 1326-1332; DOI: https://doi.org/10.1124/mol.58.6.1326

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Research ArticleArticle

Selective Abolishment of Pyrimidine Nucleoside Kinase Activity of Herpes Simplex Virus Type 1 Thymidine Kinase by Mutation of Alanine-167 to Tyrosine

Bart Degrève, Robert Esnouf, Erik De Clercq and Jan Balzarini
Molecular Pharmacology December 1, 2000, 58 (6) 1326-1332; DOI: https://doi.org/10.1124/mol.58.6.1326
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