Evidence map›Paper›PMID 36964156›Full record

ArticleNature communications2023

Transmembrane signaling by a synthetic receptor in artificial cells.

Ane Bretschneider Søgaard, Andreas Bøtker Pedersen, Kaja Borup Løvschall, Pere Monge, Josefine Hammer Jakobsen, Leila Džabbarova, Line Friis Nielsen, Sandra Stevanovic, Raoul Walther, Alexander N Zelikin

Open access · goldFull text read
In one paragraph

Article in Nature communications, 2023. 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
3.3field-weighted citation impact, top 7% 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, 35 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

10 authors at 1 institution in 1 country.

Ane Bretschneider Søgaard *Department of Chemistry, Aarhus University, Aarhus C, Denmark.ORCID 0000-0002-9603-8913
Andreas Bøtker Pedersen *Department of Chemistry, Aarhus University, Aarhus C, Denmark.ORCID 0000-0002-5481-5884
Kaja Borup LøvschallDepartment of Chemistry, Aarhus University, Aarhus C, Denmark.
Pere MongeDepartment of Chemistry, Aarhus University, Aarhus C, Denmark.
Josefine Hammer JakobsenDepartment of Chemistry, Aarhus University, Aarhus C, Denmark.
Leila DžabbarovaDepartment of Chemistry, Aarhus University, Aarhus C, Denmark.ORCID 0000-0001-5207-339X
Line Friis NielsenDepartment of Chemistry, Aarhus University, Aarhus C, Denmark.
Sandra StevanovicDepartment of Chemistry, Aarhus University, Aarhus C, Denmark.
Raoul WaltherDepartment of Chemistry, Aarhus University, Aarhus C, Denmark.ORCID 0000-0002-9833-6703
Alexander N ZelikinDepartment of Chemistry, Aarhus University, Aarhus C, Denmark. zelikin@chem.au.dk.ORCID 0000-0002-9864-321X
Aarhus University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Signal transduction across biological membranes is among the most important evolutionary achievements. Herein, for the design of artificial cells, we engineer fully synthetic receptors with the capacity of transmembrane signaling, using tools of chemistry. Our receptors exhibit similarity with their natural counterparts in having an exofacial ligand for signal capture, being membrane anchored, and featuring a releasable messenger molecule that performs enzyme activation as a downstream signaling event. The main difference from natural receptors is the mechanism of signal transduction, which is achieved using a self-immolative linker. The receptor scaffold is modular and can readily be re-designed to respond to diverse activation signals including biological or chemical stimuli. We demonstrate an artificial signaling cascade that achieves transmembrane enzyme activation, a hallmark of natural signaling receptors. Results of this work are relevant for engineering responsive artificial cells and interfacing them and/or biological counterparts in co-cultures.

Indexed as

Artificial CellsReceptors, ArtificialCarrier ProteinsCell MembraneProteinsSignal TransductionCarrier ProteinsProteinsReceptors, Artificial

Identifiers

PMID36964156
PMCPMC10039019
OpenAlexW4360826377

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read26
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.