Abstract
Fusion peptides within the coronavirus (CoV) Spike glycoprotein interact with host membranes and contribute to the structural rearrangements required for membrane fusion. Here, we investigated the upstream fusion peptide (FPu) from severe acute respiratory syndrome (SARS)-CoV and the conserved internal fusion peptide (IFP) of SARS-CoV/SARS-CoV-2 in zwitterionic and anionic lysolipid micelles using steady-state and time-resolved fluorescence, circular dichroism (CD), electron spin resonance (ESR), and molecular dynamics (MD) simulations. Both peptides strongly associated with the micellar phase, with IFP displaying higher partition coefficients and a clearer preference for negatively charged micelles. FPu exhibited pronounced environment-sensitive fluorescence changes, whereas CD revealed greater α-helical propensity for IFP and higher conformational heterogeneity for FPu. ESR showed that both peptides restricted spin-probe rotational dynamics, with broader and stronger effects in anionic micelles, particularly under acidic pH. MD simulations further indicated dynamic micelle-bound topologies in which central peptide regions were preferentially lipid-associated and less solvent-exposed, while terminal regions remained more flexible. Together, the results demonstrate that peptide affinity, conformation, bound-state topology, and perturbation of micellar dynamics are related but non-equivalent properties, highlighting the importance of membrane composition and environmental conditions in modulating coronavirus fusion-peptide interactions.
Funding Information
  • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (001)
  • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (88887.197686/2025-00)
  • Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro (200.177/2023)
  • Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro (210.094/2022)
  • Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro (211.860/2021)
  • Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro (204.310/2025)
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico (408417/2024-2)
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico (309476/2025-9)
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico (312339/2025-9)
  • Fundação de Amparo à Pesquisa do Estado de São Paulo (2025/26818-7)
  • Fundação de Amparo à Pesquisa do Estado de São Paulo (2023/04532-9)
  • Fundação de Amparo à Pesquisa do Estado de São Paulo (2021/06706-9)
  • Deutsche Forschungsgemeinschaf (SO2132/1-1)
  • Ministry of Science, Energy, Climate Protection, and Environment of the State Saxony-Anhalt
  • Universidade Estadual do Norte Fluminense Darcy Ribeiro (PAPIC UENF/PROPPG Call 05/2024)

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