Evidence map›Paper›PMID 35887325›Full record

ArticleInternational journal of molecular sciences2022

Improving the Therapeutic Index of Smp24, a Venom-Derived Antimicrobial Peptide: Increased Activity against Gram-Negative Bacteria.

Kirstie M Rawson, Melissa M Lacey, Peter N Strong, Keith Miller

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 13 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

4 authors at 1 institution in 1 country.

Kirstie M RawsonBiomolecular Sciences Research Centre, Department of Biosciences and Chemistry, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, UK.
Melissa M LaceyBiomolecular Sciences Research Centre, Department of Biosciences and Chemistry, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, UK.
Peter N StrongBiomolecular Sciences Research Centre, Department of Biosciences and Chemistry, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, UK.
Keith MillerBiomolecular Sciences Research Centre, Department of Biosciences and Chemistry, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, UK.ORCID 0000-0001-8633-6952
Sheffield Hallam University · GB

Funding

Sheffield Hallam University VC Scholarship
6 · The paper itself

Abstract

Antimicrobial peptides (AMPs) are naturally occurring compounds which possess a rapid killing mechanism and low resistance potential. Consequently, they are being viewed as potential alternatives to traditional antibiotics. One of the major factors limiting further development of AMPs is off-target toxicity. Enhancements to antimicrobial peptides which can maximise antimicrobial activity whilst reducing mammalian cytotoxicity would make these peptides more attractive as future pharmaceuticals. We have previously characterised Smp24, an AMP derived from the venom of the scorpion

Indexed as

Anti-Infective AgentsScorpion VenomsAnimalsAnti-Bacterial AgentsAntimicrobial Cationic PeptidesAntimicrobial PeptidesGram-Negative BacteriaHemolysisMammalsMicrobial Sensitivity TestsScorpionsTherapeutic IndexAnti-Bacterial AgentsAnti-Infective AgentsAntimicrobial Cationic PeptidesAntimicrobial PeptidesScorpion Venomsantimicrobial peptidepeptide modificationscorpion venom

Identifiers

PMID35887325
PMCPMC9320964
OpenAlexW4286210657

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.