Institute of Microbiology, Bulgarian Academy of Sciences, 1113, Sofia, Bulgaria.
Sorbonne Universités, UPMC Univ Paris 06, UMR_S 1138, Centre de Recherche des Cordeliers, 75006, Paris, France.
Sci Rep. 2017 Jun 19;7(1):3767. doi: 10.1038/s41598-017-03942-z.
The density and distribution pattern of epitopes at the surface of pathogens have a profound impact on immune responses. Although multiple lines of evidence highlight the significance of antigen surface density for antibody binding, a quantitative description of its effect on recognition mechanisms is missing. Here, we analyzed binding kinetics and thermodynamics of six HIV-1 neutralizing antibodies as a function of the surface density of envelope glycoprotein gp120. Antibodies that recognize gp120 with low to moderate binding affinity displayed the most pronounced sensitivity to variation in antigen density, with qualitative and substantial quantitative changes in the energetics of the binding process as revealed by non-equilibrium and equilibrium thermodynamic analyses. In contrast, the recognition of gp120 by the antibodies with the highest affinity was considerably less influenced by variations in antigen density. These data suggest that a lower affinity of antibodies permits higher dynamics during the antigen recognition process, which may have considerable functional repercussions. These findings contribute to a better understanding of the mechanisms of antigen recognition by antibodies. They are also of importance for apprehending the impact of antigen topology on immune-defense functions of antibodies.
病原体表面表位的密度和分布模式对免疫反应有深远的影响。尽管有多项证据强调了抗原表面密度对抗体结合的重要性,但对于其对识别机制的影响还缺乏定量描述。在这里,我们分析了六种 HIV-1 中和抗体作为包膜糖蛋白 gp120 表面密度函数的结合动力学和热力学。与抗原密度变化相比,识别 gp120 具有低至中等结合亲和力的抗体表现出最显著的敏感性,通过非平衡和平衡热力学分析揭示了结合过程的能量学的定性和实质性的定量变化。相比之下,与亲和力最高的抗体对 gp120 的识别受抗原密度变化的影响要小得多。这些数据表明,抗体的亲和力较低允许在抗原识别过程中具有更高的动力学,这可能具有相当大的功能影响。这些发现有助于更好地理解抗体对抗原识别的机制。它们对于理解抗原拓扑结构对抗体免疫防御功能的影响也很重要。