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秀丽隐杆线虫野生型和突变型TK1激酶的纯化与特性分析

Purification and characterization of wild-type and mutant TK1 type kinases from Caenorhabditis elegans.

作者信息

Skovgaard T, Munch-Petersen B

机构信息

Department of Life Sciences and Chemistry, Roskilde University, Roskilde, Denmark.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2006;25(9-11):1165-9. doi: 10.1080/15257770600894410.

Abstract

Caenorhabditis elegans has a single deoxynucleoside kinase-like gene. The sequence is similar to that of human TK1, but besides accepting thymidine as a substrate, the C. elegans TK1 (CeTK1) also phosphorylates deoxyguanosine. In contrast to human TK1, the CeTK1 exclusively exists as a dimer with a molecular mass of approximately 60 kDa, even if incubated with ATP. Incubation with ATP induces a transition into a more active enzyme with a higher kcat but unchanged Km. This activation only occurs at an enzyme concentration in the incubation buffer of 0.5 micro g/ml (8.42 nM) or higher. C-terminal deletion of the enzyme results in lower catalytic efficiency and stability.

摘要

秀丽隐杆线虫有一个单一的脱氧核苷激酶样基因。其序列与人类胸苷激酶1(TK1)的序列相似,但除了将胸苷作为底物外,秀丽隐杆线虫的TK1(CeTK1)还能使脱氧鸟苷磷酸化。与人类TK1不同,CeTK1仅以分子量约为60 kDa的二聚体形式存在,即使与ATP一起孵育也是如此。与ATP一起孵育会诱导其转变为一种活性更高的酶,具有更高的催化常数(kcat)但米氏常数(Km)不变。这种激活仅在孵育缓冲液中酶浓度为0.5μg/ml(8.42 nM)或更高时发生。该酶的C末端缺失会导致催化效率和稳定性降低。

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