The inositol pyrophosphate synthesis pathway in Trypanosoma brucei is linked to polyphosphate synthesis in acidocalcisomes

被引:25
作者
Cordeiro, Ciro D. [1 ,2 ]
Saiardi, Adolfo [3 ]
Docampo, Roberto [1 ,2 ]
机构
[1] Univ Georgia, Dept Cellular Biol, Athens, GA 30602 USA
[2] Univ Georgia, Ctr Trop & Emerging Global Dis, Athens, GA 30602 USA
[3] UCL, MRC, Lab Mol Cell Biol, Gower St, London WC1E 6BT, England
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
HEXAKISPHOSPHATE KINASE 1; EUKARYOTIC PHOSPHATE HOMEOSTASIS; BLOOD-STREAM FORMS; DIPHOSPHOINOSITOL POLYPHOSPHATES; HYPEROSMOTIC STRESS; PHOSPHOLIPASE-C; TELOMERE LENGTH; HUMAN HOMOLOG; CELL-DEATH; IN-VIVO;
D O I
10.1111/mmi.13766
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
Inositol pyrophosphates are novel signaling molecules possessing high-energy pyrophosphate bonds and involved in a number of biological functions. Here, we report the correct identification and characterization of the kinases involved in the inositol pyrophosphate biosynthetic pathway in Trypanosoma brucei: inositol polyphosphate multikinase (TbIPMK), inositol pentakisphosphate 2-kinase (TbIP5K) and inositol hexakisphosphate kinase (TbIP6K). TbIP5K and TbIP6K were not identifiable by sequence alone and their activities were validated by enzymatic assays with the recombinant proteins or by their complementation of yeast mutants. We also analyzed T. brucei extracts for the presence of inositol phosphates using polyacrylamide gel electrophoresis and high-performance liquid chromatography. Interestingly, we could detect inositol phosphate (IP), inositol 4,5-bisphosphate (IP2), inositol 1,4,5-trisphosphate (IP3), and inositol hexakisphosphate (IP6) in T. brucei different stages. Bloodstream forms unable to produce inositol pyrophosphates, due to downregulation of TbIPMK expression by conditional knockout, have reduced levels of polyphosphate and altered acidocalcisomes. Our study links the inositol pyrophosphate pathway to the synthesis of polyphosphate in acidocalcisomes, and may lead to better understanding of these organisms and provide new targets for drug discovery.
引用
收藏
页码:319 / 333
页数:15
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