Evidence map›Paper›PMID 37925629›Full record

ArticleMacromolecular bioscience2024

Cell Free Expression in Proteinosomes Prepared from Native Protein-PNIPAAm Conjugates.

Mengfei Gao, Dishi Wang, Michaela Wilsch-Bräuninger, Weihua Leng, Jonathan Schulte, Nina Morgner, Dietmar Appelhans, T-Y Dora Tang

Abstract read
In one paragraph

Article in Macromolecular bioscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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.

Mengfei GaoMax Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307, Dresden, Germany.
Dishi WangLeibniz-Institut für Polymerforschung Dresden e.V. Hohe Strasse 6, 01069, Dresden, Germany.
Michaela Wilsch-BräuningerMax Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307, Dresden, Germany.
Weihua LengMax Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307, Dresden, Germany.
Jonathan SchulteGoethe Universität Frankfurt, Institute of physical and theoretical chemistry, Max-von-Lauestrasse 13, 60438, Frankfurt am Main, Germany.
Nina MorgnerGoethe Universität Frankfurt, Institute of physical and theoretical chemistry, Max-von-Lauestrasse 13, 60438, Frankfurt am Main, Germany.
Dietmar AppelhansLeibniz-Institut für Polymerforschung Dresden e.V. Hohe Strasse 6, 01069, Dresden, Germany.
T-Y Dora TangMax Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307, Dresden, Germany.ORCID https://orcid.org/0000-0001-9030-6991

Funding

Deutsche Forschungsgemeinschaft 426191805Deutsche Forschungsgemeinschaft EXC-1056Deutsche Forschungsgemeinschaft EXC-2068 - 390729961Deutsche Forschungsgemeinschaft ProjectIDFederal Ministry of Education and ResearchLOEWEMax-Planck-GesellschaftMax Planck Society and the MPI-CBGMPG and MaxSynBio ConsortiumVolkswagen Foundation 92857Volkswagen Stiftung
6 · The paper itself

Abstract

Towards the goal of building synthetic cells from the bottom-up, the establishment of micrometer-sized compartments that contain and support cell free transcription and translation that couple cellular structure to function is of critical importance. Proteinosomes, formed from crosslinked cationized protein-polymer conjugates offer a promising solution to membrane-bound compartmentalization with an open, semi-permeable membrane. Critically, to date, there has been no demonstration of cell free transcription and translation within water-in-water proteinosomes. Herein, a novel approach to generate proteinosomes that can support cell free transcription and translation is presented. This approach generates proteinosomes directly from native protein-polymer (BSA-PNIPAAm) conjugates. These native proteinosomes offer an excellent alternative as a synthetic cell chassis to other membrane bound compartments. Significantly, the native proteinosomes are stable under high salt conditions that enables the ability to support cell free transcription and translation and offer enhanced protein expression compared to proteinosomes prepared from traditional methodologies. Furthermore, the integration of native proteinosomes into higher order synthetic cellular architectures with membrane free compartments such as liposomes is demonstrated. The integration of bioinspired architectural elements with the central dogma is an essential building block for realizing minimal synthetic cells and is key for exploiting artificial cells in real-world applications.

Indexed as

Artificial CellsProteinsAcrylic ResinsWaterAcrylic Resinspoly-N-isopropylacrylamideProteinsWatercell free expressioncompartmentalisationproteinosomessynthetic cells

Identifiers

PMID37925629
PMCPMC13420749

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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.