变构控制克服了靶向SARS-CoV-2刺突蛋白保守结合表位的中和抗体的空间限制:用多模态计算方法探索结合、变构和免疫逃逸的交叉点。

IF 4.8 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Biomolecules Pub Date : 2025-09-18 DOI:10.3390/biom15091340
Mohammed Alshahrani, Vedant Parikh, Brandon Foley, Gennady Verkhivker
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引用次数: 0

摘要

了解广泛反应性中和SARS-CoV-2刺突蛋白抗体所采用的多层机制的原子基础,而不直接阻断受体的参与,仍然是冠状病毒免疫学的重要挑战。第4类抗体代表了一个有趣的案例:它们靶向受体结合域上一个高度保守的隐式表位,但在不同亚群F1 (CR3022, EY6A, COVA1-16), F2 (DH1047)和F3 (S2X259)中表现出不同的中和效力。这种变异的分子基础尚未完全了解。本研究采用多模态计算方法,结合原子和粗粒度分子动力学模拟、结合自由能计算、突变扫描和动态网络分析,阐明这些抗体如何与SARS-CoV-2刺突蛋白的受体结合域(RBD)结合并影响其功能。我们的研究结果表明,中和效果来自于直接界面相互作用和变构效应的相互作用。F1组抗体(CR3022, EY6A, COVA1-16)主要通过经典的变质作用,通过远程效应调节RBD环区域的柔韧性,间接干扰ACE2受体结合。F2组抗体DH1047代表了一种中间机制,结合了部分位阻(通过结合ace2关键残基T376、R408、V503和y508)和显着的变构影响,通过将表位连接到受体界面的局部通信途径促进。F3组抗体S2X259通过与ACE2直接竞争和局部变构稳定的协同机制实现有效中和,尽管可能增加逃逸脆弱性。动态网络分析在RBD核心中发现了一个保守的“变弹性环”,作为远距离信号传播的结构支架,抗体特异性扩展调节与ACE2接口的通信。这些发现支持了一个模型,即第4类中和策略是通过外周变构连接的细化而不是表位的重新设计而进化的。本研究为理解第4类抗体中和活性和免疫逃逸的原子基础建立了一个强大的计算框架,强调了结合能量学、构象动力学和变构调节如何相互作用,从而控制了它们对抗SARS-CoV-2的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Allosteric Control Overcomes Steric Limitations for Neutralizing Antibodies Targeting Conserved Binding Epitopes of the SARS-CoV-2 Spike Protein: Exploring the Intersection of Binding, Allostery, and Immune Escape with a Multimodal Computational Approach.

Understanding the atomistic basis of multi-layer mechanisms employed by broadly reactive neutralizing antibodies of the SARS-CoV-2 spike protein without directly blocking receptor engagement remains an important challenge in coronavirus immunology. Class 4 antibodies represent an intriguing case: they target a deeply conserved, cryptic epitope on the receptor-binding domain yet exhibit variable neutralization potency across subgroups F1 (CR3022, EY6A, COVA1-16), F2 (DH1047), and F3 (S2X259). The molecular basis for this variability is not fully understood. Here, we employed a multi-modal computational approach integrating atomistic and coarse-grained molecular dynamics simulations, binding free energy calculations, mutational scanning, and dynamic network analysis to elucidate how these antibodies engage the receptor-binding domain (RBD) of the SARS-CoV-2 spike protein and influence its function. Our results reveal that neutralization efficacy arises from the interplay of direct interfacial interactions and allosteric effects. Group F1 antibodies (CR3022, EY6A, COVA1-16) primarily operate via classic allostery, modulating flexibility in RBD loop regions to indirectly interfere with the ACE2 receptor binding through long-range effects. Group F2 antibody DH1047 represents an intermediate mechanism, combining partial steric hindrance-through engagement of ACE2-critical residues T376, R408, V503, and Y508-with significant allosteric influence, facilitated by localized communication pathways linking the epitope to the receptor interface. Group F3 antibody S2X259 achieves potent neutralization through a synergistic mechanism involving direct competition with ACE2 and localized allosteric stabilization, albeit with potentially increased escape vulnerability. Dynamic network analysis identified a conserved "allosteric ring" within the RBD core that serves as a structural scaffold for long-range signal propagation, with antibody-specific extensions modulating communication to the ACE2 interface. These findings support a model where Class 4 neutralization strategies evolve through the refinement of peripheral allosteric connections rather than epitope redesign. This study establishes a robust computational framework for understanding the atomistic basis of neutralization activity and immune escape for Class 4 antibodies, highlighting how the interplay of binding energetics, conformational dynamics, and allosteric modulation governs their effectiveness against SARS-CoV-2.

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来源期刊
Biomolecules
Biomolecules Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
9.40
自引率
3.60%
发文量
1640
审稿时长
18.28 days
期刊介绍: Biomolecules (ISSN 2218-273X) is an international, peer-reviewed open access journal focusing on biogenic substances and their biological functions, structures, interactions with other molecules, and their microenvironment as well as biological systems. Biomolecules publishes reviews, regular research papers and short communications.  Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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