Evidence map›Paper›PMID 36651574›Full record

ArticleACS synthetic biology2023

Cell-Free Synthesis Goes Electric: Dual Optical and Electronic Biosensor via Direct Channel Integration into a Supported Membrane Electrode.

Zachary A Manzer, Surajit Ghosh, Arpita Roy, Miranda L Jacobs, Juliana Carten, Neha P Kamat, Susan Daniel

Abstract read
In one paragraph

Article in ACS synthetic biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Gene circuit-based sensors.Fundamental research · 2025
    Review
  4. Review
  5. 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

7 authors.

Zachary A ManzerR.F. School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, New York 14853, United States.ORCID 0000-0002-8225-8990
Surajit GhoshR.F. School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, New York 14853, United States.ORCID 0000-0003-1045-5191
Arpita RoyR.F. School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, New York 14853, United States.
Miranda L JacobsDepartment of Biomedical Engineering and Interdisciplinary Biological Sciences Program, Northwestern University, Evanston, Illinois 60208, United States.
Juliana CartenR.F. School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, New York 14853, United States.
Neha P KamatDepartment of Biomedical Engineering, Center for Synthetic Biology, Northwestern University, Evanston, Illinois 60208, United States.ORCID 0000-0001-9362-6106
Susan DanielR.F. School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, New York 14853, United States.ORCID 0000-0001-7773-0835

Funding

Training future leaders at the chemistry-biology interfaceT32GM138826 · NIGMS · CORNELL UNIVERSITY · PI Jeremy Baskin · 2021 to 2026
$2.6M
American Heart Association-American Stroke Association 20PRE35180215 - MIRANDA JACOBSNIGMS NIH HHS T32 GM138826
6 · The paper itself

Abstract

Assembling transmembrane proteins on organic electronic materials is one promising approach to couple biological functions to electrical readouts. A biosensing device produced in such a way would enable both the monitoring and regulation of physiological processes and the development of new analytical tools to identify drug targets and new protein functionalities. While transmembrane proteins can be interfaced with bioelectronics through supported lipid bilayers (SLBs), incorporating functional and oriented transmembrane proteins into these structures remains challenging. Here, we demonstrate that cell-free expression systems allow for the one-step integration of an ion channel into SLBs assembled on an organic conducting polymer, poly(3,4-ethylenedioxythiophene) polystyrenesulfonate (PEDOT:PSS). Using the large conductance mechanosensitive channel (MscL) as a model ion channel, we demonstrate that MscL adopts the correct orientation, remains mobile in the SLB, and is active on the polyelectrolyte surface using optical and electrical readouts. This work serves as an important illustration of a rapidly assembled bioelectronic platform with a diverse array of downstream applications, including electrochemical sensing, physiological regulation, and screening of transmembrane protein modulators.

Indexed as

Biosensing TechniquesLipid BilayersElectrodesElectronicsIon ChannelsMembrane ProteinsIon ChannelsLipid BilayersMembrane Proteinsbioelectroniccell-free protein synthesisdual-readoutmembrane proteinsupported lipid bilayer

Identifiers

PMID36651574
PMCPMC11364431

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Registered trials

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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.