Evidence map›Paper›PMID 40352538›Full record

ArticleACS omega2025

Affinity on Demand: A One-Pot Method for Synthesis and Sample Enrichment Using TentaGel-Functionalized Resins.

Michalina Zawadzka, Wojciech Gil, Andrzej Konieczny, Kornelia Krakowska-Jura, Monika Kijewska, Piotr Stefanowicz

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Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

6 authors.

Michalina ZawadzkaFaculty of Chemistry, University of Wrocław, Joliot-Curie 14, Wrocław 50-383, Poland.ORCID https://orcid.org/0000-0003-3185-8934
Wojciech GilFaculty of Chemistry, University of Wrocław, Joliot-Curie 14, Wrocław 50-383, Poland.
Andrzej KoniecznyDepartment of Nephrology and Transplantation Medicine, Wrocław Medical University, Borowska 213, Wrocław 50-556, Poland.
Kornelia Krakowska-JuraDepartment of Nephrology and Transplantation Medicine, Wrocław Medical University, Borowska 213, Wrocław 50-556, Poland.
Monika KijewskaFaculty of Chemistry, University of Wrocław, Joliot-Curie 14, Wrocław 50-383, Poland.ORCID https://orcid.org/0000-0001-6227-7169
Piotr StefanowiczFaculty of Chemistry, University of Wrocław, Joliot-Curie 14, Wrocław 50-383, Poland.ORCID https://orcid.org/0000-0001-9581-2359

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein glycation is a nonenzymatic reaction that results in the formation of early glycation products, commonly referred to as Amadori products, which play an important role in diabetes complications. In proteomic research, the analysis of glycated peptides is very challenging due to the low amount of analyte in a biological sample. One of the methods to overcome this is selective enrichment of the sample in the desired analyte. A method for synthesizing functionalized resins with phenylboronic acids has been developed, which allows for the incorporation of different linkers and a variable number of phenylboronic acid moieties, as well as the use of any solid support. Furthermore, the resins are prepared for use in sample enrichment following the completion of the synthesis process and demonstrate a high affinity for glycated peptides. The highest-affinity resin (4PhB-3Lys-TGR) was applied to artificially glycated albumin hydrolyzate and patient serum, and, in addition, it was used in conjunction with a biological sample (i.e., milk) for the selective enrichment of glycated peptides. The bioinformatics analysis provided results that confirmed the high coverage of protein sequences identified in the complex samples based on glycated peptides. This paper presents a novel, fast, simple, and cost-effective one-pot method for the synthesis of functionalized resins, along with a selective method for the enrichment of samples with glycated peptides. We believe that the presented approach is general and, with necessary modifications, could be applied for affinity-based isolation not only of Amadori products but also of carbonyl compounds, thiols, compounds with chelating properties, and others.

Identifiers

PMID40352538
PMCPMC12060058

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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.