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

Max O D G Baker1, Nirukshan Shanmugam1, Chi L L Pham1

  • 1Discipline of Pharmacology, School of Medical Sciences and Sydney Nano, University of Sydney, NSW, 2006, Australia.

Insights

Receptor-interacting protein kinase Homotypic Interaction Motif (RHIM) interactions are crucial for necroptosis, a cell death pathway. Pathogens target these RHIM interactions to evade immune responses and ensure survival.

Area of Science:

  • Molecular Biology
  • Immunology
  • Structural Biology

Background:

  • Receptor-interacting protein kinase Homotypic Interaction Motif (RHIM) mediates protein interactions in necroptosis, a programmed cell death pathway.
  • RHIM-based complexes can form functional amyloid structures, serving as signaling platforms.
  • RHIMs are found in immunity-related proteins across diverse organisms.

Purpose of the Study:

  • To review the structural and cell biology of RHIM:RHIM interactions in necroptosis.
  • To compare pathogen strategies for subverting RHIM interactions.
  • To explore similarities between RHIMs and other functional amyloids in immunity and cell death.

Main Methods:

  • Review of existing literature on RHIM structure, function, and interactions.
  • Comparative analysis of pathogen mechanisms targeting necroptosis.
  • Discussion of amyloid structures in the context of RHIM complexes.

Main Results:

  • RHIM:RHIM interactions are central to necroptosis activation.
  • Pathogens employ diverse strategies to inhibit RHIM interactions, facilitating infection.
  • RHIM complexes share characteristics with other functional amyloids involved in innate immunity.

Conclusions:

  • Understanding RHIM interactions is key to deciphering necroptosis regulation.
  • Pathogen manipulation of RHIMs highlights their importance in host-pathogen dynamics.
  • The amyloid nature of RHIM complexes offers insights into innate immune signaling.

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