Evidence map›Paper›PMID 33514075›Full record

ArticleJournal of proteome research2021

Enhancing Open Modification Searches via a Combined Approach Facilitated by Ursgal.

Stefan Schulze, Aime Bienfait Igiraneza, Manuel Kösters, Johannes Leufken, Sebastian A Leidel, Benjamin A Garcia, Christian Fufezan, Mechthild Pohlschroder

Abstract read
In one paragraph

Article in Journal of proteome research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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

8 authors.

Stefan SchulzeDepartment of Biology, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States.ORCID 0000-0002-4771-7987
Aime Bienfait IgiranezaDepartment of Biology, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States.
Manuel KöstersDepartment of Chemistry and Biochemistry, University of Bern, 3012 Bern, Switzerland.ORCID 0000-0002-5257-719X
Johannes LeufkenDepartment of Chemistry and Biochemistry, University of Bern, 3012 Bern, Switzerland.ORCID 0000-0001-6343-2431
Sebastian A LeidelDepartment of Chemistry and Biochemistry, University of Bern, 3012 Bern, Switzerland.
Benjamin A GarciaDepartment of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States.ORCID 0000-0002-2306-1207
Christian FufezanInstitute of Pharmacy and Molecular Biotechnology, Heidelberg University, 69120 Heidelberg, Germany.
Mechthild PohlschroderDepartment of Biology, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States.ORCID 0000-0001-7729-1342

Funding

Shared Resources Core 2: Quantitative Proteomics CoreP01CA196539 · NCI · ROCKEFELLER UNIVERSITY · PI MUIR, TOM · 2015 to 2024
$17.6M
Viral modulation of epitranscriptomic mechanismsR01AI118891 · NIAID · WASHINGTON UNIVERSITY · PI GARCIA, BENJAMIN A, WEITZMAN, MATTHEW D. · 2015 to 2025
$5.4M
A Mass Spectrometry Approach to the Genetic and Epigenetic Mechanisms Controlling Neuronal IdentityR01NS111997 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI DAHMANE, NADIA, GARCIA, BENJAMIN A · 2020 to 2024
$2.6M
NCI NIH HHS P01 CA196539NIAID NIH HHS R01 AI118891NINDS NIH HHS R01 NS111997
6 · The paper itself

Abstract

The identification of peptide sequences and their post-translational modifications (PTMs) is a crucial step in the analysis of bottom-up proteomics data. The recent development of open modification search (OMS) engines allows virtually all PTMs to be searched for. This not only increases the number of spectra that can be matched to peptides but also greatly advances the understanding of the biological roles of PTMs through the identification, and the thereby facilitated quantification, of peptidoforms (peptide sequences and their potential PTMs). Whereas the benefits of combining results from multiple protein database search engines have been previously established, similar approaches for OMS results have been missing so far. Here we compare and combine results from three different OMS engines, demonstrating an increase in peptide spectrum matches of 8-18%. The unification of search results furthermore allows for the combined downstream processing of search results, including the mapping to potential PTMs. Finally, we test for the ability of OMS engines to identify glycosylated peptides. The implementation of these engines in the Python framework Ursgal facilitates the straightforward application of the OMS with unified parameters and results files, thereby enabling yet unmatched high-throughput, large-scale data analysis.

Indexed as

AlgorithmsSoftwareDatabases, ProteinProtein Processing, Post-TranslationalProteomicsSearch Enginebioinformaticsglycosylationopen modification searchpost-translational modificationsproteomicspython

Identifiers

PMID33514075
PMCPMC8259620

What OpenQuestion holds

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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.