Evidence map›Paper›PMID 31624123›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Topological analysis of the gp41 MPER on lipid bilayers relevant to the metastable HIV-1 envelope prefusion state.

Yi Wang, Pavanjeet Kaur, Zhen-Yu J Sun, Mostafa A Elbahnasawy, Zahra Hayati, Zhi-Song Qiao, Nhat N Bui, Camila Chile, Mahmoud L Nasr, Gerhard Wagner and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. 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
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

16 citing papers in PubMed, 27 citations in OpenAlex.

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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

14 authors at 4 institutions in 1 country.

Yi WangLaboratory of Immunobiology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115.
Pavanjeet KaurNational High Magnetic Field Laboratory, Florida State University, Tallahassee, FL 32306.
Zhen-Yu J SunDepartment of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.
Mostafa A ElbahnasawyLaboratory of Immunobiology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115.
Zahra HayatiNational High Magnetic Field Laboratory, Florida State University, Tallahassee, FL 32306.
Zhi-Song QiaoLaboratory of Immunobiology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115.
Nhat N BuiNational High Magnetic Field Laboratory, Florida State University, Tallahassee, FL 32306.
Camila ChileLaboratory of Immunobiology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115.
Mahmoud L NasrDepartment of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.
Gerhard WagnerDepartment of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.
Jia-Huai WangLaboratory of Immunobiology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115.
Likai SongNational High Magnetic Field Laboratory, Florida State University, Tallahassee, FL 32306.
Ellis L ReinherzLaboratory of Immunobiology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115; ellis_reinherz@dfci.harvard.edu Mikyung_Kim@dfci.harvard.edu.
Mikyung KimLaboratory of Immunobiology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115; ellis_reinherz@dfci.harvard.edu Mikyung_Kim@dfci.harvard.edu.
Harvard University · USDana-Farber Cancer Institute · USFlorida State University · USNational High Magnetic Field Laboratory · US

Funding

Targeting Immunogenicity to the MPER Hinge and C-helix for BNAb ElicitationP01AI126901 · NIAID · DANA-FARBER CANCER INST · PI IRVINE, DARRELL J · 2016 to 2020
$9.2M
Approaches to inducing broadly neutralizing antibodies with immunogens mimicking steric occlusion of the MPER as configured on the HIV-1virion surfaceR01AI145509 · NIAID · DANA-FARBER CANCER INST · PI KIM, MIKYUNG · 2019 to 2022
$1.8M
Function of the HIV Membrane in Viral InfectionR03AI122860 · NIAID · FLORIDA STATE UNIVERSITY · PI SONG, LIKAI · 2016 to 2017
$152k
NIAID NIH HHS P01 AI126901NIAID NIH HHS R01 AI145509NIAID NIH HHS R03 AI122860
6 · The paper itself

Abstract

The membrane proximal external region (MPER) of HIV-1 envelope glycoprotein (gp) 41 is an attractive vaccine target for elicitation of broadly neutralizing antibodies (bNAbs) by vaccination. However, current details regarding the quaternary structural organization of the MPER within the native prefusion trimer [(gp120/41)

Indexed as

Antibodies, NeutralizingCell MembraneHIV-1HIV AntibodiesHIV Envelope Protein gp41HIV InfectionsHumansLipid BilayersProtein DomainsAntibodies, NeutralizingHIV AntibodiesHIV Envelope Protein gp41Lipid BilayersEnvHIV-1MPERnanodiscstransmembrane domains

Identifiers

PMID31624123
PMCPMC6842640
OpenAlexW2980804624

What OpenQuestion holds

Textmetadata
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.