Evidence map›Paper›PMID 42542529›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Generation of High-Quality Succinyl Spectral Libraries for Improved Proteome-Wide Succinylome Analysis Using Data-Independent Acquisition.

Alice Zhang, Birgit Schilling, Joanna Bons

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Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

3 authors.

Alice ZhangBuck Institute for Research on Aging, 8001 Redwood Blvd, Novato, CA, 94945, USA.
Birgit SchillingBuck Institute for Research on Aging, 8001 Redwood Blvd, Novato, CA, 94945, USA. bschilling@buckinstitute.org.
Joanna BonsBuck Institute for Research on Aging, 8001 Redwood Blvd, Novato, CA, 94945, USA. JBons@buckinstitute.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein posttranslational modifications (PTMs) are crucial and dynamic modulators of protein functions, interactions, and localizations, as well as biological pathways and cellular signaling. Lysine succinylation analysis remains challenging, but sophisticated workflows combining succinylated peptide enrichments and quantitative mass spectrometry approaches have revolutionized proteome-wide succinylome analysis. The implementation of data-independent acquisition (DIA)-mass spectrometry has greatly advanced the detection of low-abundance succinylated peptides, succinylome coverage, identification reproducibility, and quantification accuracy. However, the complexity of DIA data requires dedicated data processing algorithms and tools, which typically rely on spectral libraries. These reference libraries can be generated from experimental data-dependent acquisition (DDA) acquisitions of representative study samples submitted to DDA database search engines for confident succinylated peptide identification and precise PTM site localization. Here, we describe how to build DDA PTM spectral libraries using various software tools, specifically Spectronaut, SpectroMine, and MSFragger. The generated libraries were imported into Skyline for the analysis of previously published DIA succinylome data of Sirtuin-5 knocked-out vs wild-type mouse brains in order to accurately quantify and visualize PTM-containing peptides.

Indexed as

Protein Processing, Post-TranslationalProteomeProteomicsSuccinic AcidAnimalsDatabases, ProteinMicePeptide LibraryPeptidesSoftwareTandem Mass SpectrometryPeptide LibraryPeptidesProteomeSuccinic AcidData-dependent acquisitionData-independent acquisitionPosttranslational modificationsQuantitative proteomicsSpectral librarySuccinylation

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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.