Evidence map›Paper›PMID 31295948›Full record

ArticleMolecules (Basel, Switzerland)2019

Concentration Effects in the Interaction of Monoclonal Antibodies (mAbs) with their Immediate Environment Characterized by EPR Spectroscopy.

Haleh H Haeri, Jacob Blaffert, Florian A Schöffmann, Michaela Blech, Josef Hartl, Patrick Garidel, Dariush Hinderberger

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 30% of its field
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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Probing the YMolecules (Basel, Switzerland) · 2020
    Article
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

7 authors at 2 institutions in 1 country.

Haleh H HaeriInstitute of Chemistry, Martin Luther University Halle-Wittenberg, D06120 Halle (Saale), Germany.
Jacob BlaffertInstitute of Chemistry, Martin Luther University Halle-Wittenberg, D06120 Halle (Saale), Germany.
Florian A SchöffmannInstitute of Chemistry, Martin Luther University Halle-Wittenberg, D06120 Halle (Saale), Germany.
Michaela BlechBoehringer Ingelheim Pharma GmbH & Co. KG, Protein Science, D88397 Biberach/Riss, Germany.
Josef HartlInstitute of Chemistry, Martin Luther University Halle-Wittenberg, D06120 Halle (Saale), Germany.
Patrick GaridelInstitute of Chemistry, Martin Luther University Halle-Wittenberg, D06120 Halle (Saale), Germany.
Dariush HinderbergerInstitute of Chemistry, Martin Luther University Halle-Wittenberg, D06120 Halle (Saale), Germany. dariush.hinderberger@chemie.uni-halle.de.
Martin Luther University Halle-Wittenberg · DEBoehringer Ingelheim (Germany) · DE

Funding

European Regional Development Fund ERDF grant ZS/2016/06/79740
6 · The paper itself

Abstract

Monoclonal antibodies (mAbs) are often needed and applied in high concentration solutions, >100 mg/mL. Due to close intermolecular distances between mAbs at high concentrations (~10-20 nm at 200 mg/mL), intermolecular interactions between mAbs and mAbs and solvent/co-solute molecules become non-negligible. Here, EPR spectroscopy is used to study the high-concentration solutions of mAbs and their effect on co-solvated small molecules, using EPR "spin probing" assay in aqueous and buffered solutions. Such, information regarding the surrounding environments of mAbs at high concentrations were obtained and comparisons between EPR-obtained micro-viscosities (rotational correlation times) and macroscopic viscosities measured by rheology were possible. In comparison with highly viscous systems like glycerol-water mixtures, it was found that up to concentrations of 50 mg/mL, the mAb-spin probe systems have similar trends in their macro- (rheology) and micro-viscosities (EPR), whereas at very high concentrations they deviate strongly. The charged spin probes sense an almost unchanged aqueous solution even at very high concentrations, which in turn indicates the existence of large solvent regions that despite their proximity to large mAbs essentially offer pure water reservoirs for co-solvated charged molecules. In contrast, in buffered solutions, amphiphilic spin probes like TEMPO interact with the mAb network, due to slight charge screening. The application of EPR spectroscopy in the present work has enabled us to observe and discriminate between electrostatic and hydrophobic kinds of interactions and depict the potential underlying mechanisms of network formation at high concentrations of mAbs. These findings could be of importance as well for the development of liquid-liquid phase separations often observed in highly concentrated protein solutions.

Indexed as

Electron Spin Resonance SpectroscopyAlgorithmsAntibodies, MonoclonalGlycerolKineticsModels, ChemicalSolubilitySolventsViscosityAntibodies, MonoclonalGlycerolSolventsESR/EPR spectroscopyfluid interfacemonoclonal antibody (mAb)nitroxide spin probesprotein networksolvation

Identifiers

PMID31295948
PMCPMC6680867
OpenAlexW2961318503

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.