Evidence map›Paper›PMID 37509166›Full record

ReviewBiomolecules2023

A Frame-by-Frame Glance at Membrane Fusion Mechanisms: From Viral Infections to Fertilization.

Farshad C Azimi, Trevor T Dean, Karine Minari, Luis G M Basso, Tyler D R Vance, Vitor Hugo B Serrão

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. The SPARK complex forms the molecular basis of vertebrate fertilization.bioRxiv : the preprint server for biology · 2026
    Article
  3. Review
  4. Review
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  6. Review
  7. Review
  8. Article
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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

6 authors at 4 institutions in 3 countries.

Farshad C AzimiDepartment of Biochemistry, University of Toronto, Toronto, ON M5S 1A8, Canada.
Trevor T DeanPharmaceutical Sciences, University of Illinois Chicago, Chicago, IL 60612, USA.ORCID 0000-0002-3912-2828
Karine MinariBiomolecular Cryo-Electron Microscopy Facility, University of California-Santa Cruz, Santa Cruz, CA 95064, USA.
Luis G M BassoLaboratório de Ciências Físicas, Universidade Estadual do Norte Fluminense Darcy Ribeiro, Campos dos Goytacazes, Rio de Janeiro 28013-602, Brazil.ORCID 0000-0003-1277-1008
Tyler D R VanceDepartment of Laboratory Medicine and Pathobiology, Temerty Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada.
Vitor Hugo B SerrãoBiomolecular Cryo-Electron Microscopy Facility, University of California-Santa Cruz, Santa Cruz, CA 95064, USA.ORCID 0000-0002-9398-2941
University of California, Santa Cruz · USUniversity of Toronto · CAState University of Norte Fluminense · BRUniversity of Illinois Chicago · US

Funding

200 kV Field Emission Gun Transmission Electron Microscope for Cryo-electron MicroscopyS10OD025097 · OD · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI JURICA, MELISSA S · 2018 to 2018
$1.5M
NIH HHS S10OD02509NIH HHS S10 OD025097
6 · The paper itself

Abstract

Viral entry and fertilization are distinct biological processes that share a common mechanism: membrane fusion. In viral entry, enveloped viruses attach to the host cell membrane, triggering a series of conformational changes in the viral fusion proteins. This results in the exposure of a hydrophobic fusion peptide, which inserts into the host membrane and brings the viral and host membranes into close proximity. Subsequent structural rearrangements in opposing membranes lead to their fusion. Similarly, membrane fusion occurs when gametes merge during the fertilization process, though the exact mechanism remains unclear. Structural biology has played a pivotal role in elucidating the molecular mechanisms underlying membrane fusion. High-resolution structures of the viral and fertilization fusion-related proteins have provided valuable insights into the conformational changes that occur during this process. Understanding these mechanisms at a molecular level is essential for the development of antiviral therapeutics and tools to influence fertility. In this review, we will highlight the biological importance of membrane fusion and how protein structures have helped visualize both common elements and subtle divergences in the mechanisms behind fusion; in addition, we will examine the new tools that recent advances in structural biology provide researchers interested in a frame-by-frame understanding of membrane fusion.

Indexed as

Membrane FusionVirus DiseasesAntiviral AgentsFertilizationHumansViral Fusion ProteinsAntiviral AgentsViral Fusion Proteinscryo-electron microscopyfertilizationfusion mechanismmembrane fusionstructural biologyviruses

Identifiers

PMID37509166
PMCPMC10377500
OpenAlexW4384338532

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.