4.8 Article

Structural basis for antibody-mediated neutralization of Lassa virus

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SCIENCE
卷 356, 期 6341, 页码 923-+

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AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.aam7260

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资金

  1. NIH [1U19AI109762-01, R21 AI116112, T32 GM007491, HHSN272200900049C]
  2. Investigators in Pathogenesis of Infectious Diseases award from the Burroughs Wellcome Fund
  3. U.S. Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences [DE-AC02-76SF00515]
  4. DOE Office of Biological and Environmental Research
  5. National Institute of General Medical Sciences (NIGMS), NIH [P41GM103393]
  6. DOE Office of Science [DE-AC02-06CH11357]

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The arenavirus Lassa causes severe hemorrhagic fever and a significant disease burden in West Africa every year. The glycoprotein, GPC, is the sole antigen expressed on the viral surface and the critical target for antibody-mediated neutralization. Here we present the crystal structure of the trimeric, prefusion ectodomain of Lassa GP bound to a neutralizing antibody from a human survivor at 3.2-angstrom resolution. The antibody extensively anchors two monomers together at the base of the trimer, and biochemical analysis suggests that it neutralizes by inhibiting conformational changes required for entry. This work illuminates pH-driven conformational changes in both receptor-binding and fusion subunits of Lassa virus, illustrates the unique assembly of the arenavirus glycoprotein spike, and provides a much-needed template for vaccine design against these threats to global health.

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