ArticlePolymer chemistry2018
Self-assembly of random co-polymers for selective binding and detection of peptides.
Article in Polymer chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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.
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Who cites it
6 citing papers in PubMed.
- Tuning Net Charge in Aliphatic Polycarbonates Alters Solubility and Protein Complexation Behavior.ACS omega · 2021Article
- Polymeric nanoassemblies for enrichment and detection of peptides and proteins in human breast milk.Analytical and bioanalytical chemistry · 2020Article
- Efficient enrichment of glycopeptides by supramolecular nanoassemblies that use proximity-assisted covalent binding.The Analyst · 2019Article
- Potential of Liquid Extraction Surface Analysis Mass Spectrometry (LESA-MS) for the Characterization of Polymer-Based Materials.Polymers · 2019Review
- Supramolecular Polymeric Assemblies for the Selective Depletion of Abundant Acidic Proteins in Serum.ACS applied materials & interfaces · 2018Article
- Improved mass spectrometric detection of acidic peptides by variations in the functional group pKThe Analyst · 2018Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
Amphiphilic random co-polymers, which form stable reverse micelle-type assemblies, have been designed and synthesized. We demonstrate that the reverse micelles, formed by these co-polymers are capable of selectively binding peptides through electrostatic interactions, indicating that these random polymers can self-organize into functionally selective materials. Moreover, these random co-polymers also enable the ordered co-crystallization of matrix and extracted guest molecules, giving rise to substantial signal enhancements during MALDI-MS detection. Together, these observations represent an excellent example of how random polymers can self-assemble into ordered, functional materials.
Identifiers
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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.