Grupo de Ciencias Básicas Médicas, Facultad de Medicina, Universidad de los Andes, Bogotá, D.C., Colombia.
Acta Trop. 2012 Sep;123(3):224-9. doi: 10.1016/j.actatropica.2012.05.015. Epub 2012 Jun 8.
KMP-11 is a highly conserved protein of Trypanosoma cruzi implicated in parasite's motility. Here we show that K1, a peptide derived from KMP-11, induced polyclonal antibodies capable of decreasing T. cruzi infection in vitro. Rabbit sera rose against K1 peptide showed recognition of the recombinant protein by ELISA and Western blot and also of the native protein in both epimastigotes and trypomastigotes as evaluated by immunofluorescence test and flow cytometry. Invasion assays showed a significant reduction of trypomastigotes infection of eukaryotic cells when parasites were pre-incubated with anti-K1 rabbit serum. Computational modeling predicted that the K1 sequence conserved its α-helical configuration into the protein, and some of the amino acid residues appear accessible for recognition by antibodies in vivo. Taken together, these results support the idea that the K1 peptide induces antibodies than can have a potential role in protective immunity in Chagas disease.
KMP-11 是一种高度保守的克氏锥虫蛋白,与寄生虫的运动有关。在这里,我们表明,源自 KMP-11 的肽 K1 诱导多克隆抗体,能够降低体外的克氏锥虫感染。针对 K1 肽的兔血清通过 ELISA 和 Western blot 识别重组蛋白,也通过免疫荧光试验和流式细胞术识别原生质体和锥虫体中的天然蛋白。入侵试验表明,当寄生虫用抗 K1 兔血清预先孵育时,真核细胞中锥虫的感染显著减少。计算建模预测 K1 序列在蛋白质中保持其α-螺旋构象,并且一些氨基酸残基在体内似乎可被抗体识别。总之,这些结果支持这样一种观点,即 K1 肽诱导的抗体可能在恰加斯病的保护性免疫中发挥作用。