Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore 308232, Singapore; Department of Biology, Syracuse University, NY 13244, USA; Interdisciplinary Neuroscience Program, Syracuse University, NY 13244, USA.
Biochim Biophys Acta Biomembr. 2025 Jan;1867(1):184394. doi: 10.1016/j.bbamem.2024.184394. Epub 2024 Oct 22.
Tumor necrosis factor receptors (TNFR1 and TNFR2) play key roles in mediating inflammatory response and cell death signaling, which are associated with autoimmune disorders, neurodegenerative diseases, and cancers. The structure-function relationships of TNF receptors and their ligands determine the activation or inhibition of downstream signaling pathways. Available crystal structures have provided critical insights into the therapeutic targeting strategies of TNF receptors and their signaling networks. In this review, we discuss the potential of targeting receptor-ligand and receptor-receptor interactions in a competitive manner as well as perturbing receptor conformational dynamics through an allosteric mechanism to modulate TNF receptor signaling. We propose that conformational states of TNF receptors can act as a molecular switch in determining their functions and are important therapeutic targets. The knowledge of the structure-function relationships of TNF receptors can be applied to translational high-throughput drug screening and design of novel receptor-specific modulators with enhanced pharmacological properties.
肿瘤坏死因子受体(TNFR1 和 TNFR2)在介导炎症反应和细胞死亡信号转导中发挥着关键作用,这些反应和信号转导与自身免疫性疾病、神经退行性疾病和癌症有关。TNF 受体及其配体的结构-功能关系决定了下游信号通路的激活或抑制。现有的晶体结构为 TNF 受体及其信号网络的治疗靶向策略提供了重要的见解。在这篇综述中,我们讨论了以竞争性方式靶向受体-配体和受体-受体相互作用的潜力,以及通过变构机制干扰受体构象动力学来调节 TNF 受体信号转导的潜力。我们提出,TNF 受体的构象状态可以作为决定其功能的分子开关,是重要的治疗靶点。TNF 受体的结构-功能关系的知识可应用于转化高通量药物筛选和设计具有增强的药理学性质的新型受体特异性调节剂。