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调节胸苷激酶2活性的线粒体因子的鉴定与表征

Identification and characterization of mitochondrial factors modulating thymidine kinase 2 activity.

作者信息

Sun R, Eriksson S, Wang L

机构信息

Department of Anatomy, Section of Veterinary Medical Biochemistry, SLU, The Biomedical Centre, Uppsala, Sweden.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2010 Jun;29(4-6):382-5. doi: 10.1080/15257771003741018.

Abstract

Thymidine kinase 2 (TK2) is one of four deoxynucleoside kinases (dNKs) in humans and plays a crucial role in the initial phosphorylation of pyrimidine nucleosides in the salvage pathway in mitochondria. Nucleoside analogues, like AZT, are substrates of TK2 and induced mitochondrial toxicity in long-term therapy. We found that AZT and FLT inhibited dThd phosphorylation but stimulated dCyd phosphorylation catalyzed by TK2. However, mitochondrial phosphorylation of both dThd and dCyd was inhibited by AZT and FLT. Here a preliminary identification and characterization of mitochondrial factors is reported.

摘要

胸苷激酶2(TK2)是人类四种脱氧核苷激酶(dNKs)之一,在挽救途径中线粒体嘧啶核苷的初始磷酸化过程中起关键作用。核苷类似物,如齐多夫定(AZT),是TK2的底物,在长期治疗中会诱导线粒体毒性。我们发现AZT和氟达拉滨(FLT)抑制胸苷(dThd)磷酸化,但刺激TK2催化的胞苷(dCyd)磷酸化。然而,AZT和FLT均抑制dThd和dCyd的线粒体磷酸化。本文报道了线粒体因子的初步鉴定和表征。

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