PLoS Pathogens (Dec 2024)

Discovery of Nanosota-EB1 and -EB2 as Novel Nanobody Inhibitors Against Ebola Virus Infection.

  • Fan Bu,
  • Gang Ye,
  • Kimberly Morsheimer,
  • Alise Mendoza,
  • Hailey Turner-Hubbard,
  • Morgan Herbst,
  • Benjamin Spiller,
  • Brian E Wadzinski,
  • Brett Eaton,
  • Manu Anantpadma,
  • Ge Yang,
  • Bin Liu,
  • Robert Davey,
  • Fang Li

DOI
https://doi.org/10.1371/journal.ppat.1012817
Journal volume & issue
Vol. 20, no. 12
p. e1012817

Abstract

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The Ebola filovirus (EBOV) poses a serious threat to global health and national security. Nanobodies, a type of single-domain antibody, have demonstrated promising therapeutic potential. We identified two anti-EBOV nanobodies, Nanosota-EB1 and Nanosota-EB2, which specifically target the EBOV glycoprotein (GP). Cryo-EM and biochemical data revealed that Nanosota-EB1 binds to the glycan cap of GP1, preventing its protease cleavage, while Nanosota-EB2 binds to critical membrane-fusion elements in GP2, stabilizing it in the pre-fusion state. Nanosota-EB2 is a potent neutralizer of EBOV infection in vitro and offers excellent protection in a mouse model of EBOV challenge, while Nanosota-EB1 provides moderate neutralization and protection. Nanosota-EB1 and Nanosota-EB2 are the first nanobodies shown to inhibit authentic EBOV. Combined with our newly developed structure-guided in vitro evolution approach, they lay the foundation for nanobody-based therapies against EBOV and other viruses within the ebolavirus genus.