Doering T L, Raper J, Buxbaum L U, Adams S P, Gordon J I, Hart G W, Englund P T
Department of Biological Chemistry, Johns Hopkins Medical School, Baltimore, MD 21210.
Science. 1991 Jun 28;252(5014):1851-4. doi: 10.1126/science.1829548.
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.
布氏锥虫是导致非洲昏睡病的原生动物寄生虫,它通过抗原变异过程逃避宿主免疫反应。变异抗原,即变异表面糖蛋白(VSG),通过一种糖基磷脂酰肌醇(GPI)结构锚定在细胞表面,该结构仅含肉豆蔻酸(正十四烷酸)作为其唯一的脂肪酸成分。在无细胞系统和体内对含杂原子的肉豆蔻酸类似物的利用情况进行了研究。结果表明,脂肪酸掺入的特异性取决于链长而非疏水性。一种类似物,10 -(丙氧基)癸酸,对培养中的锥虫具有高度毒性,尽管它对哺乳动物细胞无毒。