Kumar Pranav, Kothari Hema, Singh Neeloo
Drug Target Discovery and Development Division, Central Drug Research Institute, Lucknow, India.
Protein Expr Purif. 2004 Dec;38(2):228-36. doi: 10.1016/j.pep.2004.08.015.
Pteridine reductase 1 (PTR1) is part of a novel metabolic pathway in Leishmania associated with folate metabolism. Its main function is to salvage pterins but a second one is to reduce folates. The novelty and possible uniqueness of the pathway in which PTR1 is involved opens the possibility of developing specific inhibitors, which in combination with dihydrofolate reductase inhibitors could be highly effective against Leishmania. In order to increase our understanding of this putative important chemotherapeutic target, we present here the cloning, overexpression and purification of this enzyme from a clinical isolate of Leishmania donovani causing kala azar in India. This recombinant enzyme will set the basis for inhibition studies as well as for structure-function relationships.
蝶啶还原酶1(PTR1)是利什曼原虫中与叶酸代谢相关的一条新代谢途径的一部分。其主要功能是挽救蝶呤,但第二个功能是还原叶酸。PTR1所参与的这条途径的新颖性及可能的独特性为开发特异性抑制剂提供了可能性,这些抑制剂与二氢叶酸还原酶抑制剂联合使用可能对利什曼原虫具有高效性。为了增进我们对这个假定的重要化疗靶点的了解,我们在此展示了从印度一株引起黑热病的杜氏利什曼原虫临床分离株中克隆、过表达及纯化该酶的过程。这种重组酶将为抑制研究以及结构 - 功能关系研究奠定基础。