McConville M J, Collidge T A, Ferguson M A, Schneider P
Department of Biochemistry, University of Dundee, United Kingdom.
J Biol Chem. 1993 Jul 25;268(21):15595-604.
Most macromolecules at the cell surface of parasitic protozoa of the genus Leishmania, including the major surface glycoproteins and a complex lipophosphoglycan (LPG), are attached to the plasma membrane via glycosyl-phosphatidylinositol (GPI) anchors. Free glycoinositol phospholipids (GIPLs) which are not linked to protein or phosphoglycan have also been found. In this study, we show that L. mexicana promastigotes synthesize two distinct GIPL lineages, comprising at least 10 glycolipid species. These structures were characterized using a combination of gas-liquid chromatography-mass spectrometry, methylation linkage analysis, and chemical and exoglycosidase sequencing. The major lineage contains GIPLs with the glycan structures Man alpha 1-3Man alpha 1-4GlcN (iM2), Man alpha 1-6(Man alpha 1-3)Man alpha 1-4GlcN (iM3), and Man alpha 1-2Man alpha 1-6(Man alpha 1-3)Man alpha 1-4GlcN (iM4), which are linked to alkylacyl-PI containing predominantly C16:0 and C18:0 fatty acids and C18:0 alkyl chains (referred to as the hybrid type GIPLs). A proportion of the iM3 and iM4 species (32 and 4%, respectively) are substituted with an ethanolamine-phosphate residue. The location of this residue on the core glucosamine residue was inferred from the results of methylation analyses and alpha-mannosidase digestion. The minor GIPL lineage contains GIPLs with the same glycan sequences as the glycolipid anchor of LPG (referred to as the type-2 GIPLs). The alkylacyl-PI or lyso-alkyl-PI lipid moieties of these GIPLs differ from those of the hybrid type GIPLs and from the main pool of alkylacyl-PI in containing significant levels of C24:0 and C26:0 alkyl chains. The most polar of these GIPLs, LPGp, has the properties expected of a biosynthetic precursor to the LPG, having the structure, [formula: see text] Finally, the GPI anchors of the major promastigote proteins were found to contain the glycan sequence Man alpha 1-2Man alpha 1-6Man alpha 1-4GlcN, and an alkylacyl-PI lipid moiety which was highly enriched for C24:0 or C26:0 alkyl chains. These data suggest that L. mexicana promastigotes contain three distinct pathways of GPI biosynthesis. The possibility that the distinct alkyl chain compositions of the different GPI glycolipids reflects the subcellular compartmentalization of different GPI biosynthetic pathways is discussed.
利什曼原虫属寄生原生动物细胞表面的大多数大分子,包括主要表面糖蛋白和复杂的脂磷壁酸(LPG),都是通过糖基磷脂酰肌醇(GPI)锚定连接到质膜上的。也发现了未与蛋白质或磷酸聚糖相连的游离糖肌醇磷脂(GIPL)。在本研究中,我们表明墨西哥利什曼原鞭毛体合成了两个不同的GIPL谱系,包括至少10种糖脂种类。使用气相色谱-质谱联用、甲基化连接分析以及化学和外切糖苷酶测序相结合的方法对这些结构进行了表征。主要谱系包含具有Manα1-3Manα1-4GlcN(iM2)、Manα1-6(Manα1-3)Manα1-4GlcN(iM3)和Manα1-2Manα1-6(Manα1-3)Manα1-4GlcN(iM4)糖链结构的GIPL,它们与主要含有C16:0和C18:0脂肪酸以及C18:0烷基链的烷基酰基-PI相连(称为杂合型GIPL)。一部分iM3和iM4种类(分别为32%和4%)被磷酸乙醇胺残基取代。根据甲基化分析和α-甘露糖苷酶消化的结果推断该残基在核心葡糖胺残基上的位置。次要GIPL谱系包含与LPG糖脂锚具有相同糖链序列的GIPL(称为2型GIPL)。这些GIPL的烷基酰基-PI或溶血烷基酰基-PI脂质部分与杂合型GIPL以及烷基酰基-PI的主要库不同,含有大量的C24:0和C26:0烷基链。这些GIPL中极性最大的LPGp具有LPG生物合成前体所预期的性质,其结构为[化学式:见正文]。最后,发现主要前鞭毛体蛋白的GPI锚包含糖链序列Manα1-2Manα1-6Manα1-4GlcN,以及高度富集C24:0或C26:0烷基链的烷基酰基-PI脂质部分。这些数据表明墨西哥利什曼原鞭毛体包含三种不同的GPI生物合成途径。讨论了不同GPI糖脂的不同烷基链组成反映不同GPI生物合成途径的亚细胞区室化的可能性。