Evidence map›Paper›PMID 33619482›Full record

ArticlebioRxiv : the preprint server for biology2021

Delivery of recombinant SARS-CoV-2 envelope protein into human cells.

James M Hutchison, Ricardo Capone, Dustin D Luu, Arina Hadziselimovic, Wade D Van Horn, Charles R Sanders

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

James M HutchisonChemical and Physical Biology Graduate Program, Vanderbilt University, Nashville, TN, 37240 USA.ORCID 0000-0002-5529-3248
Ricardo CaponeCenter for Structural Biology, Vanderbilt University, Nashville, TN, 37240 USA.ORCID 0000-0002-7327-9837
Dustin D LuuSchool of Molecular Sciences, Arizona State University,Tempe, AZ 85287 USA.ORCID 0000-0003-3464-160X
Arina HadziselimovicCenter for Structural Biology, Vanderbilt University, Nashville, TN, 37240 USA.
Wade D Van HornSchool of Molecular Sciences, Arizona State University,Tempe, AZ 85287 USA.ORCID 0000-0002-2493-5578
Charles R SandersCenter for Structural Biology, Vanderbilt University, Nashville, TN, 37240 USA.ORCID 0000-0003-2046-2862

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ALVIN C POWERS · 2012 to 2026
$29.3M
Shop Module CoreP30EY008126 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI David J. Calkins · 1989 to 2026
$19.6M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Roles of Cholesterol and Membrane Nanodomains in the Amyloidogenic PathwayRF1AG056147 · NIA · VANDERBILT UNIVERSITY · PI KENWORTHY, ANNE K, SANDERS, CHARLES R · 2017 to 2017
$3.6M
PIRT Family Modulation of TRPM8R01GM112077 · NIGMS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI VAN HORN, WADE D. · 2015 to 2019
$1.5M
Impact of Cholesterol and Lipid Rafts on C99 Structure and ProcessingF31AG061984 · NIA · VANDERBILT UNIVERSITY · PI HUTCHISON, JAMES M · 2019 to 2020
$60k
NCI NIH HHS P30 CA068485NEI NIH HHS P30 EY008126NIA NIH HHS F31 AG061984NIA NIH HHS RF1 AG056147NIDDK NIH HHS P30 DK020593NIDDK NIH HHS P30 DK058404NIDDK NIH HHS U24 DK059637NIGMS NIH HHS R01 GM112077
6 · The paper itself

Abstract

SARS-CoV-2 envelope protein (S2-E) is a conserved membrane protein that is essential to coronavirus assembly and budding. Here, we describe the recombinant expression and purification of S2-E into amphipol-class amphipathic polymer solutions. The physical properties of amphipols underpin their ability to solubilize and stabilize membrane proteins without disrupting membranes. Amphipol delivery of S2-E to pre-formed planar bilayers results in spontaneous membrane integration and formation of viroporin ion channels. Amphipol delivery of the S2-E protein to human cells results in membrane integration followed by retrograde trafficking to a location adjacent to the endoplasmic reticulum-to-Golgi intermediate compartment (ERGIC) and the Golgi, which are the sites of coronavirus replication. Delivery of S2-E to cells enables both chemical biological approaches for future studies of SARS-CoV-2 pathogenesis and development of "Trojan Horse" anti-viral therapies. This work also establishes a paradigm for amphipol-mediated delivery of membrane proteins to cells.

Identifiers

PMID33619482
PMCPMC7899446

What OpenQuestion holds

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LicenceCC BY-NC
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.