Evidence map›Paper›PMID 38055723›Full record

ArticlePLoS pathogens2023

Regulation of Ebola GP conformation and membrane binding by the chemical environment of the late endosome.

Aastha Jain, Ramesh Govindan, Alex R Berkman, Jeremy Luban, Marco A Díaz-Salinas, Natasha D Durham, James B Munro

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 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
2.7field-weighted citation impact, top 9% 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, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Aastha JainDepartment of Microbiology and Physiological Systems, UMass Chan Medical School, Worcester, Massachusetts, United States of America.
Ramesh GovindanDepartment of Microbiology and Physiological Systems, UMass Chan Medical School, Worcester, Massachusetts, United States of America.
Alex R BerkmanDepartment of Microbiology and Physiological Systems, UMass Chan Medical School, Worcester, Massachusetts, United States of America.
Jeremy LubanProgram in Molecular Medicine, UMass Chan Medical School, Worcester, Massachusetts, United States of America.
Marco A Díaz-SalinasDepartment of Microbiology and Physiological Systems, UMass Chan Medical School, Worcester, Massachusetts, United States of America.
Natasha D DurhamDepartment of Microbiology and Physiological Systems, UMass Chan Medical School, Worcester, Massachusetts, United States of America.
James B MunroDepartment of Microbiology and Physiological Systems, UMass Chan Medical School, Worcester, Massachusetts, United States of America.ORCID 0000-0001-7634-4633
University of Massachusetts Chan Medical School · USTufts University · US

Funding

Insight into the Ebola virus glycoprotein fusion mechanism gleaned from the 2013-2016 epidemic GP-A82V variantR01AI148784 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LUBAN, JEREMY · 2020 to 2024
$4.1M
Dynamics and mechanisms of filovirus envelop glycoproteinsR01AI174645 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI James B Munro · 2022 to 2026
$3.9M
Biophysical studies of viral membrane fusion proteinsR01GM143773 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI MUNRO, JAMES B, SOMASUNDARAN, MOHAN · 2022 to 2025
$2.1M
NIAID NIH HHS R01 AI148784NIAID NIH HHS R01 AI174645NIGMS NIH HHS R01 GM143773
6 · The paper itself

Abstract

Interaction between the Ebola virus envelope glycoprotein (GP) and the endosomal membrane is an essential step during virus entry into the cell. Acidic pH and Ca2+ have been implicated in mediating the GP-membrane interaction. However, the molecular mechanism by which these environmental factors regulate the conformational changes that enable engagement of GP with the target membrane is unknown. Here, we apply fluorescence correlation spectroscopy (FCS) and single-molecule Förster resonance energy transfer (smFRET) imaging to elucidate how the acidic pH, Ca2+ and anionic phospholipids in the late endosome promote GP-membrane interaction, thereby facilitating virus entry. We find that bis(monoacylglycero)phosphate (BMP), which is specific to the late endosome, is especially critical in determining the Ca2+-dependence of the GP-membrane interaction. Molecular dynamics (MD) simulations suggested residues in GP that sense pH and induce conformational changes that make the fusion loop available for insertion into the membrane. We similarly confirm residues in the fusion loop that mediate GP's interaction with Ca2+, which likely promotes local conformational changes in the fusion loop and mediates electrostatic interactions with the anionic phospholipids. Collectively, our results provide a mechanistic understanding of how the environment of the late endosome regulates the timing and efficiency of virus entry.

Indexed as

EbolavirusHemorrhagic Fever, EbolaCalciumEndosomesHumansHydrogen-Ion ConcentrationMembrane FusionProtein ConformationViral Envelope ProteinsVirus InternalizationCalciumViral Envelope Proteins

Identifiers

PMID38055723
PMCPMC10727438
OpenAlexW4389371704

What OpenQuestion holds

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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.