TNF receptors: Structure-function relationships and therapeutic targeting strategies

被引:5
作者
Lo, Chih Hung [1 ,2 ,3 ]
机构
[1] Nanyang Technol Univ, Lee Kong Chian Sch Med, Singapore 308232, Singapore
[2] Syracuse Univ, Dept Biol, Syracuse, NY 13244 USA
[3] Syracuse Univ, Interdisciplinary Neurosci Program, Syracuse, NY 13244 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2025年 / 1867卷 / 01期
关键词
TNF receptor; Receptor-ligand interaction; Receptor-receptor interaction; Conformational dynamics; Conformational states; FRET biosensor; Drug discovery; Antibody; Small molecule; Peptide; TUMOR-NECROSIS-FACTOR; LIGAND ASSEMBLY DOMAIN; SELECTIVE-INHIBITION; TRANSMEMBRANE DOMAIN; SMALL MOLECULES; ANTI-TNF; ALPHA; DEATH; BINDING; DISCOVERY;
D O I
10.1016/j.bbamem.2024.184394
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页数:10
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