AN ANALOG OF MYRISTIC ACID WITH SELECTIVE TOXICITY FOR AFRICAN TRYPANOSOMES

被引:73
作者
DOERING, TL
RAPER, J
BUXBAUM, LU
ADAMS, SP
GORDON, JI
HART, GW
ENGLUND, PT
机构
[1] MONSANTO CO,ST LOUIS,MO 64167
[2] WASHINGTON UNIV,SCH MED,DEPT MOLEC BIOL & PHARMACOL,ST LOUIS,MO 63110
关键词
D O I
10.1126/science.1829548
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Trypanosoma brucei, the protozoan parasite responsible for African sleeping sickness, evades the host immune response through the process of antigenic variation. The variant antigen, known as the variant surface glycoprotein (VSG), is anchored to the cell surface by a glycosyl phosphatidylinositol (GPI) structure that contains myristate (n-tetradecanoate) as its only fatty acid component. The utilization of heteroatom-containing analogs of myristate was studied both in a cell-free system and in vivo. Results indicated that the specificity of fatty acid incorporation depends on chain length rather than on hydrophobicity. One analog, 10-(propoxy)decanoic acid, was highly toxic to trypanosomes in culture although it is nontoxic to mammalian cells.
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页码:1851 / 1854
页数:4
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