RHIM-based protein:protein interactions in microbial defence against programmed cell death by necroptosis

Semin Cell Dev Biol. 2020 Mar:99:86-95. doi: 10.1016/j.semcdb.2018.05.004. Epub 2018 May 22.

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.

Keywords: Amyloid; Functional amyloid; Herpesvirus; Necroptosis; RHIM.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Apoptosis / immunology*
  • Humans
  • Immunity, Innate / immunology
  • Necroptosis / immunology*
  • Protein Binding
  • Receptor-Interacting Protein Serine-Threonine Kinases / immunology*
  • Receptor-Interacting Protein Serine-Threonine Kinases / metabolism

Substances

  • Receptor-Interacting Protein Serine-Threonine Kinases