ArticleSmall (Weinheim an der Bergstrasse, Germany)2025
Colloidal Crystallization of Virus-Like Particles with Polycations.
Article in Small (Weinheim an der Bergstrasse, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Colloidal Crystallization of Virus-Like Particles with Polycations.Small (Weinheim an der Bergstrasse, Germany) · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
Virus-like particles (VLPs) are protein nanocages capable of encapsulating or attaching guest molecules. Unlike viruses, they do not replicate in cells, making them promising candidates for advanced biomaterial design, particularly for biomedical applications such as drug delivery. However, the mechanisms governing VLPs self-assembly into highly ordered suprastructures with enhanced functionality remain largely unexplored. This study investigates the development of pH-responsive biomaterials using the icosahedral Acinetobacter phage coat protein AP205 VLPs, which has a diameter of ≈28 nm. Small-angle X-ray scattering, dynamic light scattering, and zeta-potential measurements reveal that AP205 VLPs self-assemble with the polycation poly[2-(methacryloyloxy)ethyl] trimethylammonium chloride (pMETAC) into highly ordered suprastructures. The structural organization is strongly influenced by composition, pH, and ionic strength. The findings provide insights into the directional interactions governing VLPs self-assembly with polycations and can guide the design of advanced, tunable VLP-based biomaterials.
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Registered trials
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.