Evidence map›Paper›PMID 39785238›Full record

ArticleAnalytical chemistry2025

Rational Modification of a Cross-Linker for Improved Flexible Protein Structure Modeling.

Iakovos Saridakis, Kish R Adoni, Thomas Leischner, Bogdan R Brutiu, Saad Shaaban, Giammarco Ferrari, Konstantinos Thalassinos, Nuno Maulide

Abstract read
In one paragraph

Article in Analytical chemistry, 2025. 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

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

2 citing papers in PubMed.

  1. Article
  2. Review
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.

Iakovos SaridakisInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Wien, Austria.ORCID 0000-0002-2690-5401
Kish R AdoniInstitute of Structural and Molecular Biology, Division of Biosciences, University College London, Darwin Building Room 101A, London WC1E 6BT, United Kingdom.ORCID 0000-0001-7390-501X
Thomas LeischnerInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Wien, Austria.
Bogdan R BrutiuInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Wien, Austria.ORCID 0000-0003-3952-8120
Saad ShaabanInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Wien, Austria.
Giammarco FerrariInstitute of Structural and Molecular Biology, Division of Biosciences, University College London, Darwin Building Room 101A, London WC1E 6BT, United Kingdom.
Konstantinos ThalassinosInstitute of Structural and Molecular Biology, Division of Biosciences, University College London, Darwin Building Room 101A, London WC1E 6BT, United Kingdom.ORCID 0000-0001-5072-8428
Nuno MaulideInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Wien, Austria.ORCID 0000-0003-3643-0718

Funding

Wellcome Trust
6 · The paper itself

Abstract

Chemical cross-linking/mass spectrometry (XL-MS) has emerged as a complementary tool for mapping interaction sites within protein networks as well as gaining moderate-resolution native structural insight with minimal interference. XL-MS technology mostly relies on chemoselective reactions (cross-linking) between protein residues and a linker. DSSO represents a versatile cross-linker for protein structure investigation and in-cell XL-MS. However, our assessment of its shelf life and batch purity revealed decomposition of DSSO in anhydrous solution via a retro-Michael reaction, which may reduce the active ingredient down to below 90%. To mitigate the occurrence of this degradative mechanism, we report the rational design and synthesis of DSSO-carbamate, which contains an inserted nitrogen atom in the DSSO backbone structure. This modification to DSSO yielded remarkably favorable stability against such decomposition, which translated to higher cross-link and monolink recovery when performing XL-MS on monomeric flexible proteins. Recently, XL-MS has been leveraged against AlphaFold2 and other protein structure prediction algorithms for improved prediction of flexible monomeric multiconformational proteins. To this end, we demonstrate that our novel cross-linker, termed DSSO-carbamate, generated more accurate protein structure predictions when combined with AlphaFold2, on account of its increased recovery of cross-links and monolinks, compared to DSSO. As such, DSSO-carbamate represents a useful addition to the XL-MS community, particularly for protein structure prediction.

Indexed as

CarbamatesCross-Linking ReagentsProteinsMass SpectrometryModels, MolecularProtein ConformationCarbamatesCross-Linking ReagentsProteins

Identifiers

PMID39785238
PMCPMC11755394

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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.