Biochemistry and Diseases Research Group, Facultad de Medicina, Universidad de Cartagena, Cartagena, 130015, Colombia.
Grupo de Investigaciones Biomédicas-GIB, Universidad de San Buenaventura, Cartagena, 130010, Colombia.
Parasitol Res. 2021 May;120(5):1789-1797. doi: 10.1007/s00436-021-07135-6. Epub 2021 Apr 2.
Invasion of Plasmodium into the red blood cell involves the interactions of a substantial number of proteins, with red cell membrane proteins as the most involved throughout the process from entry to exit. The objective of this work was to identify proteins of the human erythrocyte membrane capable of generating an antigenic response to P. falciparum and P. vivax infection, with the goal of searching for new molecular targets of interest with an immunological origin to prevent Plasmodium infection. To identify these proteins, an immunoproteomic technique was carried out in four stages: protein separation (electrophoresis), detection of antigenic proteins (western blotting), identification of proteins of interest (mass spectrometry), and interpretation of the data (bioinformatic analysis). Four proteins were identified from extracts of membrane proteins from erythrocytes infected with P. falciparum: Spectrin, Ankyrin-1, Band 3 and band 4.2, and a single protein was identified from erythrocytes infected with P. vivax: Band 3. These results demonstrate that modifications in the red blood cell membrane during infection with P. falciparum and P. vivax can generate an immune response, altering proteins of great structural and functional importance.
疟原虫侵入红细胞涉及大量蛋白质的相互作用,在从进入到退出的整个过程中,红细胞膜蛋白的参与最多。这项工作的目的是鉴定能够对恶性疟原虫和间日疟原虫感染产生抗原反应的人红细胞膜蛋白,以寻找具有免疫起源的新的、感兴趣的分子靶标来预防疟原虫感染。为了鉴定这些蛋白质,我们在四个阶段进行了免疫蛋白质组学技术:蛋白质分离(电泳)、抗原蛋白检测(western blot)、感兴趣蛋白鉴定(质谱)和数据解释(生物信息学分析)。从感染恶性疟原虫和间日疟原虫的红细胞膜蛋白提取物中鉴定出 4 种蛋白:血影蛋白、锚蛋白-1、带 3 和带 4.2,从感染间日疟原虫的红细胞中鉴定出 1 种蛋白:带 3。这些结果表明,恶性疟原虫和间日疟原虫感染期间红细胞膜的改变可以产生免疫反应,改变具有重要结构和功能的蛋白质。