Evidence map›Paper›PMID 38785532›Full record

ArticleCurrent issues in molecular biology2024

Effect of the 35 nm and 70 nm Size Exclusion Chromatography (SEC) Column and Plasma Storage Time on Separated Extracellular Vesicles.

Bernadett György, Krisztina Pálóczi, Mirjam Balbisi, Lilla Turiák, László Drahos, Tamás Visnovitz, Erika Koltai, Zsolt Radák

Abstract read
In one paragraph

Article in Current issues in molecular biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

8 authors.

Bernadett GyörgyResearch Centre for Molecular Exercise Science, Hungarian University of Sport Science, Alkotás u. 42-48, 1123 Budapest, Hungary.ORCID 0000-0002-3787-7338
Krisztina PálócziDepartment of Genetics, Cell and Immunobiology, Semmelweis University, Üllői út 26, 1085 Budapest, Hungary.ORCID 0000-0001-7065-3582
Mirjam BalbisiResearch Centre for Natural Sciences, Institute of Organic Chemistry, Magyar Tudósok Körútja 2, 1117 Budapest, Hungary.ORCID 0000-0002-6917-6974
Lilla TuriákResearch Centre for Natural Sciences, Institute of Organic Chemistry, Magyar Tudósok Körútja 2, 1117 Budapest, Hungary.ORCID 0000-0002-2139-8156
László DrahosResearch Centre for Natural Sciences, Institute of Organic Chemistry, Magyar Tudósok Körútja 2, 1117 Budapest, Hungary.ORCID 0000-0001-9589-6652
Tamás VisnovitzDepartment of Genetics, Cell and Immunobiology, Semmelweis University, Üllői út 26, 1085 Budapest, Hungary.ORCID 0000-0002-7962-5083
Erika KoltaiResearch Centre for Molecular Exercise Science, Hungarian University of Sport Science, Alkotás u. 42-48, 1123 Budapest, Hungary.
Zsolt RadákResearch Centre for Molecular Exercise Science, Hungarian University of Sport Science, Alkotás u. 42-48, 1123 Budapest, Hungary.ORCID 0000-0003-1297-6804

Funding

EU's Horizon 2020 Research and Innovation Programme No. 739593Hungarian National Research, Development and Innovation Office 2019-2.1.7-ERA-NET-2021-00015Hungarian National Research, Development and Innovation Office NVKP_16-1-2016-0004Hungarian National Research, Development and Innovation Office TKP2021-EGA-23Hungarian National Research, Development and Innovation Office TKP2021-EGA-37Hungarian National Research, Development and Innovation Office VEKOP-2.3.2-16-2016-00002Hungarian National Research, Development and Innovation Office VEKOP-2.3.3-15-2017-00016National Cardiovascular Laboratory Program RRF-2.3.1-21-2022-00003National Science and Research Foundation OTKA 142192Semmelweis Innovation Fund STIA 2020 KFI
6 · The paper itself

Abstract

The technical difficulty of separating extracellular vesicles (EVs) from plasma proteins in human blood presents a significant hurdle in EV research, particularly during nano ultra-high-performance liquid chromatography-tandem mass spectrometric (UHPLC-MS/MS) analysis, where detecting "vesicular" proteins among abundant plasma proteins is challenging. Standardisation is a pressing issue in EV research, prompting collaborative global efforts to address it. While the MISEV guidelines offer valuable recommendations, unanswered questions remain, particularly regarding sample storage. We compared size exclusion chromatography (SEC) columns with pore sizes of 35 nm and 70 nm to identify fractions with minimal contaminating proteins and the highest concentration of small EVs (sEVs). Following column selection, we explored potential differences in the quality and quantity of sEVs isolated from platelet-free plasma (PFP) after long-term storage at -80 °C (>2.5 years) compared to freshly drawn blood. Our methodologically rigorous study indicates that prolonged storage, under correct storage and processing conditions, does not compromise sEV quality. Both columns effectively isolated vesicles, with the 70 nm column exhibiting a higher abundance of "vesicular" proteins. We propose a relatively rapid and moderately efficient protocol for obtaining a comparatively pure sEV fraction from plasma, facilitating sEV processing in clinical trials.

Indexed as

extracellular vesicleshuman plasmamass spectrometrysize exclusion chromatographystorage time

Identifiers

PMID38785532
PMCPMC11120626

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Registered trials

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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.