Evidence map›Paper›PMID 34163978›Full record

ArticleChemical science2021

Activating mechanosensitive channels embedded in droplet interface bilayers using membrane asymmetry.

Robert Strutt, James W Hindley, Jordan Gregg, Paula J Booth, John D Harling, Robert V Law, Mark S Friddin, Oscar Ces

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed, 28 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

8 authors at 3 institutions in 3 countries.

Robert StruttDepartment of Chemistry, Imperial College London, Molecular Sciences Research Hub Shepherd's Bush London W12 0BZ UK o.ces@imperial.ac.uk.ORCID https://orcid.org/0000-0003-0979-2000
James W HindleyDepartment of Chemistry, Imperial College London, Molecular Sciences Research Hub Shepherd's Bush London W12 0BZ UK o.ces@imperial.ac.uk.ORCID https://orcid.org/0000-0002-3392-4387
Jordan GreggDepartment of Chemistry, Imperial College London, Molecular Sciences Research Hub Shepherd's Bush London W12 0BZ UK o.ces@imperial.ac.uk.
Paula J BoothFabriCELL, Imperial College London, Molecular Sciences Research Hub Shepherd's Bush London W12 0BZ UK.
John D HarlingMedicinal Chemistry, GSK Gunnels Wood Road, Stevenage SG1 2NY UK.
Robert V LawDepartment of Chemistry, Imperial College London, Molecular Sciences Research Hub Shepherd's Bush London W12 0BZ UK o.ces@imperial.ac.uk.
Mark S FriddinDepartment of Chemistry, Imperial College London, Molecular Sciences Research Hub Shepherd's Bush London W12 0BZ UK o.ces@imperial.ac.uk.ORCID https://orcid.org/0000-0003-4421-8792
Oscar CesDepartment of Chemistry, Imperial College London, Molecular Sciences Research Hub Shepherd's Bush London W12 0BZ UK o.ces@imperial.ac.uk.ORCID https://orcid.org/0000-0002-6418-5644
Transnational Press LondonAge UK · GBWiCell · US

Funding

Wellcome Trust 214259
6 · The paper itself

Abstract

Droplet microcompartments linked by lipid bilayers show great promise in the construction of synthetic minimal tissues. Central to controlling the flow of information in these systems are membrane proteins, which can gate in response to specific stimuli in order to control the molecular flux between membrane separated compartments. This has been demonstrated with droplet interface bilayers (DIBs) using several different membrane proteins combined with electrical, mechanical, and/or chemical activators. Here we report the activation of the bacterial mechanosensitive channel of large conductance (MscL) in a dioleoylphosphatidylcholine:dioleoylphosphatidylglycerol DIB by controlling membrane asymmetry. We show using electrical measurements that the incorporation of lysophosphatidylcholine (LPC) into one of the bilayer leaflets triggers MscL gating in a concentration-dependent manner, with partial and full activation observed at 10 and 15 mol% LPC respectively. Our findings could inspire the design of new minimal tissues where flux pathways are dynamically defined by lipid composition.

Identifiers

PMID34163978
PMCPMC8179348
OpenAlexW3120762599

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.