Evidence map›Paper›PMID 38751636›Full record

ArticleACS pharmacology & translational science2024

Innovative Reversed-Phase Chromatography Platform Approach for the Fast and Accurate Characterization of Membrane Vesicles' Protein Patterns.

Luca Nompari, Salvatore Sanna Coccone, Gian Luca Sardone, Alessio Corrado, Stefania Berti, Massimiliano Biagini, Michele Rovini, Claudia Magagnoli, Simona Cianetti, Serena Orlandini and 2 more

Abstract read
In one paragraph

Article in ACS pharmacology & translational science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Luca NompariGSK, Technical Research and Development (TRD), Via Fiorentina 1, 53100 Siena, Italy.
Salvatore Sanna CocconeGSK, Technical Research and Development (TRD), Via Fiorentina 1, 53100 Siena, Italy.
Gian Luca SardoneGSK, Technical Research and Development (TRD), Via Fiorentina 1, 53100 Siena, Italy.
Alessio CorradoGSK, Technical Research and Development (TRD), Via Fiorentina 1, 53100 Siena, Italy.
Stefania BertiGSK, Technical Research and Development (TRD), Via Fiorentina 1, 53100 Siena, Italy.
Massimiliano BiaginiGSK, Technical Research and Development (TRD), Via Fiorentina 1, 53100 Siena, Italy.
Michele RoviniGSK, Technical Research and Development (TRD), Via Fiorentina 1, 53100 Siena, Italy.
Claudia MagagnoliGSK, Technical Research and Development (TRD), Via Fiorentina 1, 53100 Siena, Italy.
Simona CianettiGSK, Technical Research and Development (TRD), Via Fiorentina 1, 53100 Siena, Italy.
Serena OrlandiniDepartment of Chemistry "U. Schiff″, University of Florence, Via U. Schiff 6, Sesto Fiorentino 50019, Florence, Italy.
Sandra FurlanettoDepartment of Chemistry "U. Schiff″, University of Florence, Via U. Schiff 6, Sesto Fiorentino 50019, Florence, Italy.
Riccardo De RiccoGSK, Technical Research and Development (TRD), Via Fiorentina 1, 53100 Siena, Italy.ORCID https://orcid.org/0000-0003-2387-7780

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Outer membrane vesicles (OMVs) have been widely explored to develop vaccine candidates for bacterial pathogens due to their ability to combine adjuvant properties with immunogenic activity. OMV expresses a variety of proteins and carbohydrate antigens on their surfaces. For this reason, there is an analytical need to thoroughly characterize the species expressed at their surface: we here present a simple and accurate reversed-phase ultrahigh-performance liquid chromatography (RP-UPLC) method developed according to quality by design principles. This work provides an analytical alternative to the classical sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) characterization. The higher selectivity and sensitivity of the RP-UHPLC assay allow for the identification of additional protein species with respect to SDS-PAGE and facilitate its precise relative abundance quantification. According to validation results, the assay showed high accuracy, linearity, precision, repeatability, and a limit of quantification of 1% for less abundant proteins. This performance paves the way for improved production campaign consistency while also being analytically simple (no sample pretreatment required), making it suitable for routine quality control testing. In addition, the applicability of the assay to a wider range of vesicle classes (GMMA) was demonstrated.

Identifiers

PMID38751636
PMCPMC11091982

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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.