Evidence map›Paper›PMID 33349334›Full record

ArticleeLife2020

Molecular rationale for antibody-mediated targeting of the hantavirus fusion glycoprotein.

Ilona Rissanen, Robert Stass, Stefanie A Krumm, Jeffrey Seow, Ruben Jg Hulswit, Guido C Paesen, Jussi Hepojoki, Olli Vapalahti, Åke Lundkvist, Olivier Reynard and 4 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.5field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 5 countries.

Ilona Rissanen *Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Robert Stass *Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Stefanie A KrummDepartment of Infectious Diseases, King's College London, Guy's Hospital, London, United Kingdom.
Jeffrey SeowDepartment of Infectious Diseases, King's College London, Guy's Hospital, London, United Kingdom.
Ruben Jg HulswitDivision of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Guido C PaesenDivision of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Jussi HepojokiInstitute of Veterinary Pathology, Vetsuisse Faculty, University of Zürich, Zürich, Switzerland.
Olli VapalahtiDepartments of Virology and Veterinary Biosciences, University of Helsinki and HUSLAB, Helsinki University Hospital, Helsinki, Finland.
Åke LundkvistZoonosis Science Center, Department of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.
Olivier ReynardCIRI, Centre International de Recherche en Infectiologie, INSERM U1111, CNRS UMR5308, Université Lyon, Lyon, France.
Viktor VolchkovCIRI, Centre International de Recherche en Infectiologie, INSERM U1111, CNRS UMR5308, Université Lyon, Lyon, France.
Katie J DooresDepartment of Infectious Diseases, King's College London, Guy's Hospital, London, United Kingdom.
Juha T HuiskonenDivision of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-0348-7323
Thomas A BowdenDivision of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-8066-8785
Centre for Human Genetics · GBGuy's Hospital · GBUniversité Claude Bernard Lyon 1 · FRUniversity of Helsinki · FIUppsala University · SE

Funding

Medical Research Council MR/K024426/1Medical Research Council MR/L009528/1Medical Research Council MR/N002091/1Medical Research Council MR/S007555/1Wellcome TrustWellcome Trust 060208/Z/00/ZWellcome Trust 093305/Z/10/ZWellcome Trust 203141/Z/16Z
6 · The paper itself

Abstract

The intricate lattice of Gn and Gc glycoprotein spike complexes on the hantavirus envelope facilitates host-cell entry and is the primary target of the neutralizing antibody-mediated immune response. Through study of a neutralizing monoclonal antibody termed mAb P-4G2, which neutralizes the zoonotic pathogen Puumala virus (PUUV), we provide a molecular-level basis for antibody-mediated targeting of the hantaviral glycoprotein lattice. Crystallographic analysis demonstrates that P-4G2 binds to a multi-domain site on PUUV Gc and may preclude fusogenic rearrangements of the glycoprotein that are required for host-cell entry. Furthermore, cryo-electron microscopy of PUUV-like particles in the presence of P-4G2 reveals a lattice-independent configuration of the Gc, demonstrating that P-4G2 perturbs the (Gn-Gc)

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralArvicolinaeHEK293 CellsHumansPuumala virusViral Fusion ProteinsAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralViral Fusion Proteinsglycoproteinhantavirusinfectious diseasemicrobiologymolecular biophysicsneutralizing antibodystructural biologystructureviral fusionvirus

Identifiers

PMID33349334
PMCPMC7755396
OpenAlexW3117476806

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.