Evidence map›Paper›PMID 33651392›Full record

ArticleElectrophoresis2021

Online hyphenation of size-exclusion chromatography and gas-phase electrophoresis facilitates the characterization of protein aggregates.

Victor U Weiss, Natalia Denderz, Günter Allmaier, Martina Marchetti-Deschmann

Abstract read
In one paragraph

Article in Electrophoresis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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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

4 authors.

Victor U WeissInstitute for Chemical Technologies and Analytics, TU Wien (Vienna University of Technology), Vienna, Austria.ORCID 0000-0002-0056-6819
Natalia DenderzInstitute for Chemical Technologies and Analytics, TU Wien (Vienna University of Technology), Vienna, Austria.
Günter AllmaierInstitute for Chemical Technologies and Analytics, TU Wien (Vienna University of Technology), Vienna, Austria.ORCID 0000-0002-1438-9462
Martina Marchetti-DeschmannInstitute for Chemical Technologies and Analytics, TU Wien (Vienna University of Technology), Vienna, Austria.ORCID 0000-0002-8060-7851

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gas-phase electrophoresis yields size distributions of polydisperse, aerosolized analytes based on electrophoretic principles. Nanometer-sized, surface-dry, single-charged particles are separated in a high laminar sheath flow of particle-free air and an orthogonal tunable electric field. Additionally, nano Electrospray Gas-Phase Electrophoretic Mobility Molecular Analyzer (nES GEMMA) data are particle-number based. Therefore, small particles can be detected next to larger ones without a bias, for example, native proteins next to their aggregates. Analyte transition from the liquid to the gas phase is a method inherent prerequisite. In this context, nonvolatile sample buffers influence results. In the worst case, the (bio-)nanoparticle signal is lost due to an increased baseline and unspecific clustering of nonvolatile components. We present a novel online hyphenation of liquid chromatography and gas-phase electrophoresis, coupling a size-exclusion chromatography (SEC) column to an advanced nES GEMMA. Via this novel approach, it is possible to (i) separate analyte multimers already present in liquid phase from aggregates formed during the nES process, (ii) differentiate liquid phase and spray-induced multimers, and (iii) to remove nonvolatile buffer components online before SEC-nES GEMMA analysis. Due to these findings, SEC-nES GEMMA has the high potential to help to understand aggregation processes in biological buffers adding the benefit of actual size determination for noncovalent assemblies formed in solution. As detection and characterization of protein aggregation in large-scale pharmaceutical production or sizing of noncovalently bound proteins are findings directly related to technologically and biologically relevant situations, we proposed the presented method to be a valuable addition to LC-MS approaches.

Indexed as

Chromatography, GelElectrophoresisProtein AggregatesProteinsProtein AggregatesProteinsMacroIMSnES DMAnES GEMMAProtein aggregatesSize-exclusion chromatography

Identifiers

PMID33651392
PMCPMC8252587

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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.