Evidence map›Paper›PMID 39873636›Full record

ArticleBiochemistry2025

Carboxy-Amidated AamAP1-Lys has Superior Conformational Flexibility and Accelerated Killing of Gram-Negative Bacteria.

Rosalind J Van Wyk, June C Serem, Carel B Oosthuizen, Dorothy Semenya, Miruna Serian, Christian D Lorenz, A James Mason, Megan J Bester, Anabella R M Gaspar

Abstract read
In one paragraph

Article in Biochemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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

9 authors.

Rosalind J Van WykDepartment of Biochemistry, Genetics and Microbiology, Faculty of Natural and Agricultural Sciences, University of Pretoria, Pretoria 0002, South Africa.
June C SeremDepartment of Anatomy, Faculty of Health Sciences, University of Pretoria, Pretoria 0002, South Africa.
Carel B OosthuizenDrug Discovery and Development Centre (H3D), University of Cape Town, Cape Town 7701, South Africa.ORCID 0000-0003-0940-8099
Dorothy SemenyaInstitute of Pharmaceutical Science, School of Cancer & Pharmaceutical Sciences, King's College London, London SE1 9NH, United Kingdom.
Miruna SerianDepartment of Physics, Faculty of Natural, Mathematical and Engineering Sciences, King's College London, London WC2R 2LS, United Kingdom.
Christian D LorenzDepartment of Engineering, Faculty of Natural, Mathematical and Engineering Sciences, King's College London, London WC2R 2LS, United Kingdom.ORCID 0000-0003-1028-4804
A James MasonInstitute of Pharmaceutical Science, School of Cancer & Pharmaceutical Sciences, King's College London, London SE1 9NH, United Kingdom.ORCID 0000-0003-0411-602X
Megan J BesterDepartment of Anatomy, Faculty of Health Sciences, University of Pretoria, Pretoria 0002, South Africa.
Anabella R M GasparDepartment of Biochemistry, Genetics and Microbiology, Faculty of Natural and Agricultural Sciences, University of Pretoria, Pretoria 0002, South Africa.ORCID 0000-0003-2035-3084

Funding

Medical Research Council MC_PC_MR/T029552/1
6 · The paper itself

Abstract

C-terminal amidation of antimicrobial peptides (AMPs) is a frequent minor modification used to improve antibacterial potency, commonly ascribed to increased positive charge, protection from proteases, and a stabilized secondary structure. Although the activity of AMPs is primarily associated with the ability to penetrate bacterial membranes, hitherto the effect of amidation on this interaction has not been understood in detail. Here, we show that amidation of the scorpion-derived membranolytic peptide AamAP1-Lys produces a potent analog with faster bactericidal activity, increased membrane permeabilization, and greater Gram-negative membrane penetration associated with greater conformational flexibility. AamAP1-lys-NH

Indexed as

Acinetobacter baumanniiAnti-Bacterial AgentsAntimicrobial Cationic PeptidesAntimicrobial PeptidesEscherichia coliAnimalsBiofilmsCircular DichroismMicrobial Sensitivity TestsMolecular Dynamics SimulationProtein ConformationAnti-Bacterial AgentsAntimicrobial Cationic PeptidesAntimicrobial Peptides

Identifiers

PMID39873636
PMCPMC11840929

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.