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碘珠表面标记的马来布鲁线虫微丝蚴主要抗原的免疫化学特性及生物合成

Immunochemical characterization and biosynthesis of major antigens of iodo-bead surface-labeled Brugia malayi microfilariae.

作者信息

Egwang T G, Kazura J W

出版信息

Mol Biochem Parasitol. 1987 Jan 15;22(2-3):159-68. doi: 10.1016/0166-6851(87)90046-6.

Abstract

The objectives of the present study were to identify and characterize biochemically the major antigens of Brugia malayi microfilariae, a filarial parasite that infects humans. IgG antibodies in sera of mice which had cleared parasites from the bloodstream reacted with 30, 55, 94 and 150 kDa molecules of living microfilariae radioiodinated by the Iodo-bead method. Sera of humans infected with the related filariae Wuchereria bancrofti, Loa loa or Onchocerca volvulus immunoprecipitated molecules of similar size as well as two additional proteins of 22 and 43 kDa. Sera of uninfected North Americans or mice infected with Trichinella spiralis or Schistosoma mansoni did not recognize these radioiodinated antigens. Experiments to examine the possible surface localization and metabolism of these antigens showed that they were removed from intact parasites exposed to chymotrypsin or trypsin and that immunogenic molecules of 30, 55, and 150 kDa were released into excretory-secretory products by viable microfilariae. [35S]Methionine biosynthetically labeled polypeptide antigens of 22, 30, 35 and 150 kDa were detected by antibody reacted with intact microfilariae and/or their excretion products. Antigens of 30, 55, and 150 kDa appear to be glycoproteins as they bound wheat germ agglutinin and were biosynthetically labeled with [14C]N-acetyl-D-glucosamine. These data suggest that the surface of B. malayi microfilariae is a dynamic structure which synthesizes and sheds antigens.

摘要

本研究的目的是对马来布鲁线虫微丝蚴(一种感染人类的丝虫寄生虫)的主要抗原进行生化鉴定和特性分析。已清除血液中寄生虫的小鼠血清中的IgG抗体与通过碘珠法放射性碘化的活微丝蚴的30、55、94和150 kDa分子发生反应。感染相关丝虫班氏吴策线虫、罗阿丝虫或盘尾丝虫的人类血清免疫沉淀出大小相似的分子以及另外两种22和43 kDa的蛋白质。未感染的北美人群或感染旋毛虫或曼氏血吸虫的小鼠血清未识别这些放射性碘化抗原。检测这些抗原可能的表面定位和代谢的实验表明,它们可从暴露于胰凝乳蛋白酶或胰蛋白酶的完整寄生虫中去除,并且30、55和150 kDa的免疫原性分子可由活微丝蚴释放到排泄-分泌产物中。通过与完整微丝蚴和/或其排泄产物反应的抗体检测到了22、30、35和150 kDa的[35S]蛋氨酸生物合成标记的多肽抗原。30、55和150 kDa的抗原似乎是糖蛋白,因为它们与麦胚凝集素结合并被[14C]N-乙酰-D-葡萄糖胺生物合成标记。这些数据表明,马来布鲁线虫微丝蚴的表面是一个动态结构,可合成并释放抗原。

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