Driscoll Paul C
Division of Molecular Structure, Medical Research Council, National Institute for Medical Research, London, United Kingdom.
Methods Enzymol. 2014;545:201-42. doi: 10.1016/B978-0-12-801430-1.00009-3.
This chapter describes reports of the structural characterization of death ligands and death receptors (DRs) from the tumor necrosis factor (TNF) and TNF receptor families. The review discusses the interactions of these proteins with agonist ligands, inhibitors, and downstream signaling molecules. Though historically labeled as being implicated in programmed cell death, the function of these proteins extends to nonapoptotic pathways. The review highlights, from a structural biology perspective, the complexity of DR signaling and the ongoing challenge to discern the precise mechanisms that occur at the point of DR activation, including how the degree to which the receptors are induced to cluster may be related to the nature of the impact upon the cell. The potential for posttranslational modification and receptor internalization to play roles in DR signaling is briefly discussed.
本章描述了来自肿瘤坏死因子(TNF)和TNF受体家族的死亡配体和死亡受体(DRs)的结构特征报告。该综述讨论了这些蛋白质与激动剂配体、抑制剂和下游信号分子的相互作用。尽管这些蛋白质在历史上被标记为与程序性细胞死亡有关,但其功能已扩展到非凋亡途径。该综述从结构生物学的角度强调了DR信号传导的复杂性,以及在识别DR激活时发生的精确机制方面持续存在的挑战,包括受体被诱导聚集的程度如何可能与对细胞的影响性质相关。还简要讨论了翻译后修饰和受体内化在DR信号传导中发挥作用的可能性。