Alphaviral Capsid Proteins Inhibit Stress Granule Assembly via Competitive RNA Binding With G3BP1

Adv Sci (Weinh). 2026 Apr;13(20):e17009. doi: 10.1002/advs.202517009. Epub 2026 Jan 27.

Abstract

Viral infection is one of the conditions that induce stress granule (SG) formation, a cellular defense mechanism that exerts antiviral effects. To counteract this host response, viruses have evolved a broad spectrum of strategies to inhibit SG formation. However, the molecular mechanisms underlying SG inhibition remain poorly understood. The nucleocapsid proteins play a critical role in virus replication and host interaction. Here, using Semliki Forest Virus (SFV) as a model, we uncover the function of the alphavirus nucleocapsid in SG inhibition. This inhibitory function depends on oligomerization mediated by an N-terminal α-helix and with a positively charged intrinsically disordered region (IDR). We show that SFV capsid directly competes with G3BP1 for RNA binding, thereby disrupting G3BP1-RNA liquid-liquid phase separation (LLPS) in vitro and SG assembly in cells. This mechanism is conserved across the alphavirus family but is not shared by the nucleocapsid of SARS-CoV-2 or other endemic viruses examined. Notably, expression of a peptide from SFV capsid is sufficient to inhibit SG formation induced by Amyotrophic Lateral Sclerosis (ALS)-associated mutations, suggesting potential therapeutic applications. Our findings reveal mechanistic insight into SG modulation by the viral capsid protein and provide a possible bioengineering tool for probing SG dynamics in health and disease.

Keywords: G3BP1; alphavirus capsid; biomolecular condensates; phase separation; stress granule.

MeSH terms

  • Alphavirus / metabolism
  • Animals
  • Capsid Proteins* / genetics
  • Capsid Proteins* / metabolism
  • DNA Helicases / metabolism
  • Humans
  • Poly-ADP-Ribose Binding Proteins* / genetics
  • Poly-ADP-Ribose Binding Proteins* / metabolism
  • RNA Helicases* / metabolism
  • RNA Recognition Motif Proteins* / genetics
  • RNA Recognition Motif Proteins* / metabolism
  • SARS-CoV-2 / metabolism
  • Semliki forest virus* / genetics
  • Semliki forest virus* / metabolism
  • Stress Granules* / metabolism
  • Virus Replication

Substances

  • RNA Recognition Motif Proteins
  • G3BP1 protein, human
  • Poly-ADP-Ribose Binding Proteins
  • Capsid Proteins
  • RNA Helicases
  • DNA Helicases