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抗原密度对 IgG 抗体结合机制的影响。

Impact of Antigen Density on the Binding Mechanism of IgG Antibodies.

机构信息

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.

出版信息

Sci Rep. 2017 Jun 19;7(1):3767. doi: 10.1038/s41598-017-03942-z.

DOI:10.1038/s41598-017-03942-z
PMID:28630473
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5476644/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd3/5476644/c92787ae7e3b/41598_2017_3942_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd3/5476644/30b2aae8348d/41598_2017_3942_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd3/5476644/057d8d8ce103/41598_2017_3942_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd3/5476644/bb396ef7a0a3/41598_2017_3942_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd3/5476644/8ddfcf05c29f/41598_2017_3942_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd3/5476644/c92787ae7e3b/41598_2017_3942_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd3/5476644/30b2aae8348d/41598_2017_3942_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd3/5476644/057d8d8ce103/41598_2017_3942_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd3/5476644/bb396ef7a0a3/41598_2017_3942_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd3/5476644/8ddfcf05c29f/41598_2017_3942_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd3/5476644/c92787ae7e3b/41598_2017_3942_Fig5_HTML.jpg

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J Immunol. 2016 Sep 1;197(5):1762-75. doi: 10.4049/jimmunol.1600648. Epub 2016 Jul 29.
2
Simulation and Theory of Antibody Binding to Crowded Antigen-Covered Surfaces.抗体与拥挤抗原覆盖表面结合的模拟与理论
PLoS Comput Biol. 2016 Mar 11;12(3):e1004752. doi: 10.1371/journal.pcbi.1004752. eCollection 2016 Mar.
3
A Novel Platform for the Potentiation of Therapeutic Antibodies Based on Antigen-Dependent Formation of IgG Hexamers at the Cell Surface.
Cell Rep Med. 2024 Nov 19;5(11):101800. doi: 10.1016/j.xcrm.2024.101800. Epub 2024 Oct 25.
4
A new silicon phthalocyanine dye induces pyroptosis in prostate cancer cells during photoimmunotherapy.一种新型硅酞菁染料在光免疫治疗过程中可诱导前列腺癌细胞发生焦亡。
Bioact Mater. 2024 Aug 16;41:537-552. doi: 10.1016/j.bioactmat.2024.07.025. eCollection 2024 Nov.
5
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JACS Au. 2024 Jul 31;4(8):2792-2810. doi: 10.1021/jacsau.4c00568. eCollection 2024 Aug 26.
6
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Biochim Biophys Acta Gen Subj. 2023 Nov;1867(11):130448. doi: 10.1016/j.bbagen.2023.130448. Epub 2023 Aug 29.
7
Cholera intoxication of human enteroids reveals interplay between decoy and functional glycoconjugate ligands.人类类器官的霍乱毒素中毒揭示了诱饵和功能性糖缀合物配体之间的相互作用。
Glycobiology. 2023 Oct 30;33(10):801-816. doi: 10.1093/glycob/cwad069.
8
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9
Modelling ligand depletion for simultaneous affinity and binding site quantification on cells and tissue.对细胞和组织上的配体消耗进行建模,以同时进行亲和力和结合位定量分析。
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10
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Protein Sci. 2022 Nov;31(11):e4447. doi: 10.1002/pro.4447.
一种基于细胞表面IgG六聚体的抗原依赖性形成来增强治疗性抗体的新型平台。
PLoS Biol. 2016 Jan 6;14(1):e1002344. doi: 10.1371/journal.pbio.1002344. eCollection 2016 Jan.
4
Complement System Part I - Molecular Mechanisms of Activation and Regulation.补体系统 第一部分——激活与调节的分子机制
Front Immunol. 2015 Jun 2;6:262. doi: 10.3389/fimmu.2015.00262. eCollection 2015.
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6
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7
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Nature. 2013 Apr 25;496(7446):469-76. doi: 10.1038/nature12053. Epub 2013 Apr 3.