Evidence map›Paper›PMID 41893725›Full record

ArticleProteomes2026

Comparison of the Trapping Efficiency for Tryptic Peptides on Particle-Packed and Micro-Pillar Trap Columns for Proteomics Analyses.

Jadranka Miletić Vukajlović, Bojana Ilić, Bella Bruszel, Tanja Panić-Janković, Goran Mitulović

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Article in Proteomes, 2026. 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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5 · Who and what money

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5 authors.

Jadranka Miletić VukajlovićDepartment of Physical Chemistry, Vinča Institute of Nuclear Sciences, National Institute of the Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0002-9873-1906
Bojana IlićDepartment of Physical Chemistry, Vinča Institute of Nuclear Sciences, National Institute of the Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0003-4271-4370
Bella BruszelInstitute of Science and Technology, 3400 Klosterneuburg, Austria.ORCID 0000-0001-5154-4735
Tanja Panić-JankovićKlinik Landstrasse, Zentrallaboratorium mit Blutbank, Juchgasse 25, 1030 Vienna, Austria.ORCID 0000-0001-6569-4398
Goran MitulovićDepartment of Laboratory Medicine, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0003-1964-3965

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLow-volume trapping columns are essential for sample enrichment, desalting, and injection profile focusing on nano-LC-MS-based proteomics. They enable higher sample loading, improve chromatographic performance, and protect the analytical column by removing salts and contaminants. Recently, monolithic trap columns with micropillar architecture have emerged as alternatives to conventionally packed traps. This study compares the performance of a packed and a micropillar monolithic trap column for the analysis of tryptic peptides.

methodsA tryptic digest of HeLa cell lysate was analyzed under identical LC-MS conditions using both trap types. Peptides were detected at 214 nm and analyzed by nano-ESI on a Q Exactive Plus Orbitrap. Data were searched against the human UniProt database (February 2023) using FragPipe v20.0, and statistical evaluation of MaxLFQ intensities was performed in Perseus using Welch's

resultsOver 2500 proteins were identified with both setups. The packed trap column yielded more total peptides, particularly those with post-translational modifications and higher hydrophilicity, whereas the monolithic column favored peptides of intermediate hydrophobicity. Chromatographic profiles confirmed a slight reduction in the trapping efficiency of hydrophilic peptides by the monolithic trap.

conclusionsTrap column design significantly influences peptide recovery and proteome coverage.

Indexed as

high-performance liquid chromatographypeptide identificationproteomicstrap columns

Identifiers

PMID41893725
PMCPMC13030385

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