tetano
Editor, Senior Moderator
Nat Commun
. 2025 Jun 3;16(1):5150.
doi: 10.1038/s41467-025-60406-z. Unveiling the structural spectrum of SARS-CoV-2 fusion by in situ cryo-ET
Caner Akıl[SUP] #[/SUP][SUP] 1 2 [/SUP], Jialu Xu[SUP] #[/SUP][SUP] 2 [/SUP], Juan Shen[SUP] 2 [/SUP], Peijun Zhang[SUP] 3 4 5 [/SUP]
Affiliations
SARS-CoV-2 entry into host cells is mediated by the spike protein, which drives membrane fusion. While cryo-EM reveals stable prefusion and postfusion conformations of the spike, the transient fusion intermediate states during the fusion process remain poorly understood. Here, we design a near-native viral fusion system that recapitulates SARS-CoV-2 entry and use cryo-electron tomography (cryo-ET) to capture fusion intermediates leading to complete fusion. The spike protein undergoes extensive structural rearrangements, progressing through extended, partially folded, and fully folded intermediates prior to fusion-pore formation, a process that depends on protease cleavage and is inhibited by the WS6 S2 antibody. Upon interaction with ACE2 receptor dimer, spikes cluster at membrane interfaces and following S2' cleavage concurrently transition to postfusion conformations encircling the hemifusion and initial fusion pores in a distinct conical arrangement. S2' cleavage is indispensable for advancing fusion intermediates to the fully folded postfusion state, culminating in membrane integration. Subtomogram averaging reveals that the WS6 S2 antibody binds to the spike's stem-helix, crosslinks and clusters prefusion spikes, as well as inhibits refolding of fusion intermediates. These findings elucidate the entire process of spike-mediated fusion and SARS-CoV-2 entry, highlighting the neutralizing mechanism of S2-targeting antibodies.
. 2025 Jun 3;16(1):5150.
doi: 10.1038/s41467-025-60406-z. Unveiling the structural spectrum of SARS-CoV-2 fusion by in situ cryo-ET
Caner Akıl[SUP] #[/SUP][SUP] 1 2 [/SUP], Jialu Xu[SUP] #[/SUP][SUP] 2 [/SUP], Juan Shen[SUP] 2 [/SUP], Peijun Zhang[SUP] 3 4 5 [/SUP]
Affiliations
- PMID: 40461447
- PMCID: PMC12134289
- DOI: 10.1038/s41467-025-60406-z
SARS-CoV-2 entry into host cells is mediated by the spike protein, which drives membrane fusion. While cryo-EM reveals stable prefusion and postfusion conformations of the spike, the transient fusion intermediate states during the fusion process remain poorly understood. Here, we design a near-native viral fusion system that recapitulates SARS-CoV-2 entry and use cryo-electron tomography (cryo-ET) to capture fusion intermediates leading to complete fusion. The spike protein undergoes extensive structural rearrangements, progressing through extended, partially folded, and fully folded intermediates prior to fusion-pore formation, a process that depends on protease cleavage and is inhibited by the WS6 S2 antibody. Upon interaction with ACE2 receptor dimer, spikes cluster at membrane interfaces and following S2' cleavage concurrently transition to postfusion conformations encircling the hemifusion and initial fusion pores in a distinct conical arrangement. S2' cleavage is indispensable for advancing fusion intermediates to the fully folded postfusion state, culminating in membrane integration. Subtomogram averaging reveals that the WS6 S2 antibody binds to the spike's stem-helix, crosslinks and clusters prefusion spikes, as well as inhibits refolding of fusion intermediates. These findings elucidate the entire process of spike-mediated fusion and SARS-CoV-2 entry, highlighting the neutralizing mechanism of S2-targeting antibodies.