Evidence map›Paper›PMID 39720905›Full record

ArticleProtein science : a publication of the Protein Society2025

In situ characterization of amine-forming enzymes shows altered oligomeric state.

Adam A Caparco, Bettina R Bommarius, Laurine Ducrot, Julie A Champion, Carine Vergne-Vaxelaire, Andreas S Bommarius

Abstract read
In one paragraph

Article in Protein science : a publication of the Protein Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. In situ characterization of amine-forming enzymes shows altered oligomeric state.Protein science : a publication of the Protein Society · 2025
    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

6 authors.

Adam A CaparcoSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia, USA.ORCID 0000-0002-8545-8349
Bettina R BommariusSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia, USA.ORCID 0000-0002-1283-0218
Laurine DucrotGénomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS, Univ Evry, Université Paris-Saclay, Evry, France.ORCID 0000-0002-6423-4573
Julie A ChampionSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia, USA.ORCID 0000-0002-0260-9392
Carine Vergne-VaxelaireGénomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS, Univ Evry, Université Paris-Saclay, Evry, France.ORCID 0000-0002-1202-8110
Andreas S BommariusSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia, USA.ORCID 0000-0003-4658-1675

Funding

Commissariat à l'énergie atomique et aux énergies alternatives (CEA, France)Conseil National de la Recherche ScientifiqueNSF-CBET 1512848NSF I/UCRC 1540017University of Evry Paris-Saclay (France)
6 · The paper itself

Abstract

Enzyme stability can be measured in a number of ways, including melting temperature, activity retention, and size analysis. However, these measurements are often conducted in an idealized storage buffer and not in the relevant enzymatic reaction media. Particularly for reactions that occur in alkaline, volatile, and high ionic strength media, typical analyses using differential scanning calorimetry, light scattering, and sodium dodecyl-sulfate polyacrylamide gel electrophoresis are not satisfactory to track the stability of these enzymes. In this work, we monitor the stability of engineered and native dehydrogenases that require a high amount of ammonia for their reaction to occur. We demonstrate the benefits of analyzing these enzymes in their reaction buffer, uncovering trends that were not observable in the typical phosphate storage buffer. This work provides a framework for analyzing the stability of many other enzymes whose reaction media is not suitable for traditional techniques. We introduce several strategies for measuring the melting temperature, oligomeric state, and activity of these enzymes in their reaction media. Further, we have identified opportunities for integration of computational tools into this workflow to engineer enzymes more effectively for solvent tolerance and improved stability.

Indexed as

Enzyme StabilityAminesAmmoniaProtein MultimerizationAminesAmmoniaamine dehydrogenasebiophysical characterizationin situ characterizationprotein engineering

Identifiers

PMID39720905
PMCPMC11669115

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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.