Thiol metabolism of the trypanosomatids as potential drug targets

被引:20
作者
Steenkamp, DJ [1 ]
机构
[1] Univ Cape Town, Fac Hlth Sci, Div Chem Pathol, ZA-7935 Observatory, South Africa
关键词
glutathionylspermidine; leishmania; ovothiol A; trypanosoma; trypanothione; trypanothione reductase;
D O I
10.1080/15216540212649
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Trypanosomatids produce significant amounts of four major low molecular mass thiols, trypanothione, glutathionylspermidine, glutathione, and ovothiol A. Of these, only glutathione is present in cells of the host. All four low molecular mass thiols are directly or indirectly maintained in a reduced state by trypanothione reductase. Available evidence, from gene disruption studies, indicate that this is an essential enzyme. Attempts to exploit trypanothione reductase as a chemotherapeutic target lead to the design of competitive and irreversible inhibitors of the enzyme. A promising route involves the design of redox cyclers interacting specifically with trypanothione reductase as subversive substrates. Progress in studies on the biosynthesis of ovothiol A is summarized.
引用
收藏
页码:243 / 248
页数:6
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