Evidence map›Paper›PMID 37602460›Full record

ArticleACS applied materials & interfaces2023

Combinatorial Screening of Cationic Lipidoids Reveals How Molecular Conformation Affects Membrane-Targeting Antimicrobial Activity.

James Jennings, Dunja Ašćerić, Enrico Federico Semeraro, Karl Lohner, Nermina Malanovic, Georg Pabst

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. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Bactericidal Activity toAntibiotics (Basel, Switzerland) · 2023
    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

6 authors.

James JenningsInstitute of Molecular Biosciences, University of Graz, NAWI Graz, 8010 Graz, Austria.ORCID 0000-0003-1213-4607
Dunja AšćerićInstitute of Molecular Biosciences, University of Graz, NAWI Graz, 8010 Graz, Austria.
Enrico Federico SemeraroInstitute of Molecular Biosciences, University of Graz, NAWI Graz, 8010 Graz, Austria.ORCID 0000-0002-6096-1108
Karl LohnerInstitute of Molecular Biosciences, University of Graz, NAWI Graz, 8010 Graz, Austria.
Nermina MalanovicInstitute of Molecular Biosciences, University of Graz, NAWI Graz, 8010 Graz, Austria.
Georg PabstInstitute of Molecular Biosciences, University of Graz, NAWI Graz, 8010 Graz, Austria.ORCID 0000-0003-1967-1536

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The search for next-generation antibacterial compounds that overcome the development of resistance can be facilitated by identifying how to target the cell membrane of bacteria. Understanding the key molecular features that enable interactions with lipids and lead to membrane disruption is therefore crucial. Here, we employ a library of lipid-like compounds (lipidoids) comprising modular structures with tunable hydrophobic and hydrophilic architecture to shed light on how the chemical functionality and molecular shape of synthetic amphiphilic compounds determine their activity against bacterial membranes. Synthesized from combinations of 8 different polyamines as headgroups and 13 acrylates as tails, 104 different lipidoids are tested for activity against a model Gram-positive bacterial strain (

Indexed as

Anti-Bacterial AgentsCationsCell MembraneMembranesScattering, Small AngleX-Ray DiffractionAnti-Bacterial AgentsCationscombinatorial synthesislipidoidsmembrane-active compoundsquaternary ammonium compoundssmall-angle X-ray scattering

Identifiers

PMID37602460
PMCPMC10472336

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.