Evidence map›Paper›PMID 40026451›Full record

ArticleMacromolecules2025

Presenting Antimicrobial Peptides on Poly(ethylene glycol): Star-Shaped vs Comb-Like Architectures.

Zixian Cui, Elliot A Brna, Matthew A Crawford, Puthayalai Treerat, Mobina Alimadad, Molly A Hughes, Rachel A Letteri

Abstract read
In one paragraph

Article in Macromolecules, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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.

Zixian CuiDepartment of Chemical Engineering, University of Virginia, Charlottesville, Virginia 22903, United States.
Elliot A BrnaDepartment of Chemical Engineering, University of Virginia, Charlottesville, Virginia 22903, United States.
Matthew A CrawfordDivision of Infectious Diseases & International Health, Department of Medicine, University of Virginia, Charlottesville, Virginia 22908, United States.ORCID https://orcid.org/0000-0003-0404-0061
Puthayalai TreeratDivision of Infectious Diseases & International Health, Department of Medicine, University of Virginia, Charlottesville, Virginia 22908, United States.
Mobina AlimadadDepartment of Chemical Engineering, University of Virginia, Charlottesville, Virginia 22903, United States.ORCID https://orcid.org/0009-0006-1231-2951
Molly A HughesDivision of Infectious Diseases & International Health, Department of Medicine, University of Virginia, Charlottesville, Virginia 22908, United States.
Rachel A LetteriDepartment of Chemical Engineering, University of Virginia, Charlottesville, Virginia 22903, United States.ORCID https://orcid.org/0000-0002-2919-203X

Funding

A unique strategy for reshaping the antibiotics model: chemokine-inspired therapeutics for targeting the host and pathogen to counter infections caused by multidrug-resistant bacteriaR01AI150941 · NIAID · UNIVERSITY OF VIRGINIA · PI HUGHES, MOLLY A · 2020 to 2024
$3.1M
Optimizing therapeutic peptide presentation within polymersR35GM147424 · NIGMS · UNIVERSITY OF VIRGINIA · PI Rachel Letteri · 2022 to 2026
$1.8M
NIAID NIH HHS R01 AI150941NIGMS NIH HHS R35 GM147424
6 · The paper itself

Abstract

Conjugating antimicrobial peptides (AMPs) to nonlinear polymers is a promising strategy to overcome the translational challenges of AMPs toward treating infections caused by antibiotic-resistant bacteria. Nonlinear polymers, and therefore conjugates, can be prepared with various architectures (e.g., star-shaped, comb-like, hyperbranched, etc.), however, the effects of polymer architecture on antimicrobial performance and related properties, like size and morphology in solution and secondary structure, are not yet well-understood. Here, we compare conjugates of the human chemokine-derived AMP stapled P9 with poly(ethylene glycol) (PEG) prepared in two of the major nonlinear architectures: star-shaped and comb-like. At comparable molecular weights and compositions (peptide wt %), comb-like conjugates afford increased helicity, solubility, antimicrobial activity, and proteolytic stability compared to star-shaped analogs. We then leveraged the expansive design space of comb-like architectures to prepare conjugates with different backbone lengths and PEG side chain lengths, with shorter PEG side chains leading to increased helicity, yet potentially less shielding from proteolytic degradation and the longest backbone lengths furnishing the most potent antimicrobial activity. Both comb-like and star-shaped conjugates display high zeta potential, indicating that the cationic AMPs were accessible for electrostatic interactions with bacterial membranes. Yet, the comb-like conjugates showed a higher fraction of unimolecular structures indicative of a lower propensity for supramolecular assembly that could be encumbering the desired AMP-bacteria interactions in the star-shaped conjugates. Together, our work shows comb-like AMP-polymer conjugates to outperform analogous star-shaped conjugates, while adding design flexibility to access an expansive range of monomer chemistries, monomer distributions, and backbone lengths to modulate performance-determining properties and ultimately furnish an effective suite of AMP-polymer materials as alternatives to conventional antibiotics for combatting bacterial infections.

Identifiers

PMID40026451
PMCPMC11867009

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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.