Evidence map›Paper›PMID 39005468›Full record

ArticlebioRxiv : the preprint server for biology2024

Quantification and site-specific analysis of co-occupied N- and O-glycopeptides.

Joann Chongsaritsinsuk, Valentina Rangel-Angarita, Keira E Mahoney, Taryn M Lucas, Olivia M Enny, Mitchelle Katemauswa, Stacy A Malaker

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Joann ChongsaritsinsukDepartment of Chemistry, Yale University, New Haven, CT.ORCID 0000-0003-0562-2987
Valentina Rangel-AngaritaDepartment of Chemistry, Yale University, New Haven, CT.ORCID 0000-0003-3632-6160
Keira E MahoneyDepartment of Chemistry, Yale University, New Haven, CT.ORCID 0000-0003-4561-9838
Taryn M LucasDepartment of Chemistry, Yale University, New Haven, CT.ORCID 0000-0002-1697-0939
Olivia M EnnyDepartment of Chemistry, Yale University, New Haven, CT.
Mitchelle KatemauswaDepartment of Chemistry, Yale University, New Haven, CT.
Stacy A MalakerDepartment of Chemistry, Yale University, New Haven, CT.ORCID 0000-0003-2382-5067

Funding

PREDOCTORAL PROGRAM IN BIOPHYSICST32GM008283 · NIGMS · YALE UNIVERSITY · PI XIONG, YONG · 1988 to 2022
$10.5M
Toward understanding the role of altered glycosylation in cancerR35GM147039 · NIGMS · YALE UNIVERSITY · PI Stacy Alyse Malaker · 2022 to 2026
$2.0M
NIGMS NIH HHS R35 GM147039NIGMS NIH HHS T32 GM008283
6 · The paper itself

Abstract

Protein glycosylation is a complex post-translational modification that is generally classified as N- or O-linked. Site-specific analysis of glycopeptides is accomplished with a variety of fragmentation methods, depending on the type of glycosylation being investigated and the instrumentation available. For instance, collisional dissociation methods are frequently used for N-glycoproteomic analysis with the assumption that one N-sequon exists per tryptic peptide. Alternatively, electron-based methods are indispensable for O-glycosite localization. However, the presence of simultaneously N- and O-glycosylated peptides could suggest the necessity of electron-based fragmentation methods for N-glycoproteomics, which is not commonly performed. Thus, we quantified the prevalence of N- and O-glycopeptides in mucins and other glycoproteins. A much higher frequency of co-occupancy within mucins was detected whereas only a negligible occurrence occurred within non-mucin glycoproteins. This was demonstrated from analyses of recombinant and/or purified proteins, as well as more complex samples. Where co-occupancy occurred, O-glycosites were frequently localized to the Ser/Thr within the N-sequon. Additionally, we found that O-glycans in close proximity to the occupied Asn were predominantly unelaborated core 1 structures, while those further away were more extended. Overall, we demonstrate electron-based methods are required for robust site-specific analysis of mucins, wherein co-occupancy is more prevalent. Conversely, collisional methods are generally sufficient for analyses of other types of glycoproteins.

Indexed as

co-occupancyfragmentationglycoproteomicsmucinsN-glycosylationO-glycosylation

Identifiers

PMID39005468
PMCPMC11245114

What OpenQuestion holds

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LicenceCC BY
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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.