RHIM-based protein:protein interactions in microbial defence against programmed cell death by necroptosis. (March 2020)

• Record Type: Journal Article
• Authors: Baker, Max O.D.G.; Shanmugam, Nirukshan; Pham, Chi L.L.; Strange, Merryn; Steain, Megan; Sunde, Margaret
• Is Part Of: Seminars in cell & developmental biology. Volume 99(2020)
• Page Start: 86
• Page End: 95
• Publication Date: 2020-03
• Subjects: Necroptosis -- Amyloid -- RHIM -- Herpesvirus -- Functional amyloid; Cytology -- Periodicals; Developmental biology -- Periodicals; 571.6
• DOI: 10.1016/j.semcdb.2018.05.004
• Languages: English
• ISSNs: 1084-9521

Abstract

Abstract: The Receptor-interacting protein kinase Homotypic Interaction Motif (RHIM) is an amino acid sequence that mediates multiple protein:protein interactions in the mammalian programmed cell death pathway known as necroptosis. At least one key RHIM-based complex has been shown to have a functional amyloid fibril structure, which provides a stable hetero-oligomeric platform for downstream signaling. RHIMs and related motifs are present in immunity-related proteins across nature, from viruses to fungi to metazoans. Necroptosis is a hallmark feature of cellular clearance of infection. For this reason, numerous pathogens, including viruses and bacteria, have developed varied methods to modulate necroptosis, focusing on inhibiting RHIM:RHIM interactions, and thus their downstream cell death effects. This review will discuss current understanding of RHIM:RHIM interactions in normal cellular activation of necroptosis, from a structural and cell biology perspective. It will compare the mechanisms by which pathogens subvert these interactions in order to maintain their replicative and infective cycles and consider the similarities between RHIMs and other functional amyloid-forming proteins associated with cell death and innate immunity. It will discuss the implications of the heteromeric nature and structure of RHIM-based amyloid complexes in the context of other functional amyloids.