Zhou Wei, Brisson Dustin
University of Pennsylvania, 3451 Walnut Street, Philadelphia, PA 19104, United States.
University of Pennsylvania, 3451 Walnut Street, Philadelphia, PA 19104, United States.
Microbes Infect. 2017 Apr-May;19(4-5):267-276. doi: 10.1016/j.micinf.2017.01.001. Epub 2017 Jan 10.
Many parasites have evolved antigenic variation systems that alter surface proteins in order to evade recognition by presently expressed antibodies and subsequent death. Although the amino acid positions in antigens to which antibodies most commonly target are expected to be the most variable, this assumption has not been investigated. Using the vls antigenic variation system of Borrelia burgdorferi as a model, we first investigated this assumption computationally and then developed a sensitive immunoassay to experimentally validate the computational results. There was a strong correlation between variability at an amino acid position and each of the computational metrics associated with antibody reactivity. However, empirical measures of antibody reactivity were not consistently greater at the variable amino acid positions than at the invariant amino acid positions. The inconsistent experimental support for this hypothesis suggests that the biological effect of variability at an amino acid position is obfuscated by other factors.
许多寄生虫已经进化出抗原变异系统,该系统通过改变表面蛋白来逃避当前表达的抗体的识别以及随后的死亡。尽管预计抗体最常靶向的抗原中的氨基酸位置是最可变的,但这一假设尚未得到研究。我们以伯氏疏螺旋体的可变淋巴细胞特异性(vls)抗原变异系统为模型,首先通过计算研究了这一假设,然后开发了一种灵敏的免疫测定法来实验验证计算结果。氨基酸位置的变异性与每个与抗体反应性相关的计算指标之间存在很强的相关性。然而,抗体反应性的实证测量在可变氨基酸位置并不总是比在不变氨基酸位置更高。对这一假设的实验支持不一致,这表明氨基酸位置变异性的生物学效应被其他因素掩盖了。