Gurale Bharat P, He Yun, Cui Xikai, Dinh Hieu, Dhawane Abasaheb N, Lucchi Naomi W, Udhayakumar Venkatachalam, Iyer Suri S
Department of Chemistry, Center for Diagnostics and Therapeutics, Georgia State University, 788 Petit Science Center , 161 Jesse Hill Jr. Drive, Atlanta, Georgia 30302, United States.
Atlanta Research and Education Foundation , Atlanta, Georgia 30329, United States.
Bioconjug Chem. 2016 Dec 21;27(12):2886-2899. doi: 10.1021/acs.bioconjchem.6b00542. Epub 2016 Dec 1.
A large number of proteins in malaria parasites are anchored using glycophosphatidylinositols (GPIs) with lipid tails. These GPIs are structurally distinct from human GPIs. Plasmodium falciparum GPIs have been considered as potential vaccine candidates because these molecules are involved in inducing inflammatory responses in human hosts, and natural anti-GPI antibody responses have been shown to be associated with protection against severe disease. GPIs can also be considered as targets for rapid diagnostic tests. Because isolation of native GPIs in large quantities is challenging, development of synthetic GPI molecules can facilitate further exploration of GPI molecules for diagnostics. Here, we report synthesis and immunological characterization of a panel of malaria-specific GPI analogues. A total of three GPI analogues were chemically synthesized and conjugated to a carrier protein to immunize and generate antibodies in rabbits. The rabbit immune sera showed reactivity with synthetic GPIs and native GPIs extracted from P. falciparum parasite, as determined by Luminex and ELISA methods.
疟原虫中的大量蛋白质通过带有脂质尾巴的糖基磷脂酰肌醇(GPI)进行锚定。这些GPI在结构上与人类GPI不同。恶性疟原虫的GPI被认为是潜在的疫苗候选物,因为这些分子参与在人类宿主中诱导炎症反应,并且天然抗GPI抗体反应已被证明与预防严重疾病有关。GPI也可被视为快速诊断测试的靶点。由于大量分离天然GPI具有挑战性,合成GPI分子的开发可以促进对用于诊断的GPI分子的进一步探索。在此,我们报告了一组疟疾特异性GPI类似物的合成及免疫学特性。总共化学合成了三种GPI类似物,并将其与载体蛋白偶联,用于免疫兔子并产生抗体。通过Luminex和ELISA方法测定,兔免疫血清与合成GPI以及从恶性疟原虫中提取的天然GPI具有反应性。