Evidence map›Paper›PMID 37721709›Full record

ArticleACS applied materials & interfaces2023

Lipid-Functionalized Single-Walled Carbon Nanotubes as Probes for Screening Cell Wall Disruptors.

Nathaniel E Kallmyer, Sparsh Agarwal, Danielle Eeg, Rachel Khor, Nathan Roby, Alma Vela Ramirez, Andrew C Hillier, Nigel F Reuel

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2023. 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

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.

Nathaniel E KallmyerDepartment of Chemical and Biological Engineering, Iowa State University, Ames, Iowa 50011, United States.
Sparsh AgarwalDepartment of Chemical and Biological Engineering, Iowa State University, Ames, Iowa 50011, United States.
Danielle EegDepartment of Chemical and Biological Engineering, Iowa State University, Ames, Iowa 50011, United States.
Rachel KhorDepartment of Chemical and Biological Engineering, Iowa State University, Ames, Iowa 50011, United States.
Nathan RobyDepartment of Chemical and Biological Engineering, Iowa State University, Ames, Iowa 50011, United States.
Alma Vela RamirezDepartment of Chemical and Biological Engineering, Iowa State University, Ames, Iowa 50011, United States.
Andrew C HillierDepartment of Chemical and Biological Engineering, Iowa State University, Ames, Iowa 50011, United States.ORCID 0000-0002-2729-1368
Nigel F ReuelDepartment of Chemical and Biological Engineering, Iowa State University, Ames, Iowa 50011, United States.ORCID 0000-0003-3438-2919

Funding

Unsupervised optimization of protein therapeutics using closed-loop in vitro synthesis, nanosensing,and deep-learningR35GM138265 · NIGMS · IOWA STATE UNIVERSITY · PI Nigel F Reuel · 2020 to 2026
$2.3M
NIGMS NIH HHS R35 GM138265
6 · The paper itself

Abstract

Membrane-active molecules are of great importance to drug delivery and antimicrobials applications. While the ability to prototype new membrane-active molecules has improved greatly with the advent of automated chemistries and rapid biomolecule expression techniques, testing methods are still limited by throughput, cost, and modularity. Existing methods suffer from feasibility constraints of working with pathogenic living cells and by intrinsic limitations of model systems. Herein, we demonstrate an abiotic sensor that uses semiconducting single-walled carbon nanotubes (SWCNTs) as near-infrared fluorescent transducers to report membrane interactions. This sensor is composed of SWCNTs aqueously suspended in lipid, creating a cylindrical, bilayer corona; these SWCNT probes are very sensitive to solvent access (changes in permittivity) and thus report morphological changes to the lipid corona by modulation of fluorescent signals, where binding and disruption are reported as brightening and attenuation, respectively. This mechanism is first demonstrated with chemical and physical membrane-disruptive agents, including ethanol and sodium dodecyl sulfate, and application of electrical pulses. Known cell-penetrating and antimicrobial peptides are then used to demonstrate how the dynamic response of these sensors can be deconvoluted to evaluate different parallel mechanisms of interaction. Last, SWCNTs functionalized in several different bacterial lipopolysaccharides (

Indexed as

Cell WallNanotubes, CarbonEscherichia coliKlebsiella pneumoniaeLipopolysaccharidesPseudomonas aeruginosaLipopolysaccharidesNanotubes, Carboncell proxydisruptionmembranenanosensorscreening techniques

Identifiers

PMID37721709
PMCPMC11806933

What OpenQuestion holds

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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.