Evidence map›Paper›PMID 42399233›Full record

ArticleNature communications2026

High-sensitive glycomics using seGRAP-mass spectrometry uncovers a conserved N-glycome in single human oocytes.

Nafisa Tursumamat, Qiannan Liu, Jihong Lu, Shuhong Guo, Shuangshuang Du, Shengyang Liu, Shuye Wu, Heming Li, Peng Wu, Bin Li and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2026. 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

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

11 authors.

Nafisa TursumamatEngineering Research Center of Cell & Therapeutic Antibody, Ministry of Education, Shanghai Key Laboratory for Antibody-Drug Conjugates with Innovative Target, School of Pharmaceutical Sciences, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240, China.
Qiannan LiuEngineering Research Center of Cell & Therapeutic Antibody, Ministry of Education, Shanghai Key Laboratory for Antibody-Drug Conjugates with Innovative Target, School of Pharmaceutical Sciences, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240, China.
Jihong LuEngineering Research Center of Cell & Therapeutic Antibody, Ministry of Education, Shanghai Key Laboratory for Antibody-Drug Conjugates with Innovative Target, School of Pharmaceutical Sciences, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240, China.
Shuhong GuoEngineering Research Center of Cell & Therapeutic Antibody, Ministry of Education, Shanghai Key Laboratory for Antibody-Drug Conjugates with Innovative Target, School of Pharmaceutical Sciences, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240, China.
Shuangshuang DuDepartment of Assisted Reproduction, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200011, China.
Shengyang LiuEngineering Research Center of Cell & Therapeutic Antibody, Ministry of Education, Shanghai Key Laboratory for Antibody-Drug Conjugates with Innovative Target, School of Pharmaceutical Sciences, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240, China.
Shuye WuEngineering Research Center of Cell & Therapeutic Antibody, Ministry of Education, Shanghai Key Laboratory for Antibody-Drug Conjugates with Innovative Target, School of Pharmaceutical Sciences, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240, China.
Heming LiEngineering Research Center of Cell & Therapeutic Antibody, Ministry of Education, Shanghai Key Laboratory for Antibody-Drug Conjugates with Innovative Target, School of Pharmaceutical Sciences, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240, China.
Peng WuDepartment of Molecular and Cellular Biology, The Scripps Research Institute, La Jolla, CA, 92037, USA.ORCID 0000-0002-5204-0229
Bin LiDepartment of Assisted Reproduction, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200011, China. lib3036@sh9hospital.org.cn.ORCID 0000-0001-7838-4399
Juan WeiEngineering Research Center of Cell & Therapeutic Antibody, Ministry of Education, Shanghai Key Laboratory for Antibody-Drug Conjugates with Innovative Target, School of Pharmaceutical Sciences, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240, China. wwwjuan@sjtu.edu.cn.ORCID 0000-0002-8621-6253

Funding

National Natural Science Foundation of China (National Science Foundation of China) No. 82204330
6 · The paper itself

Abstract

High-sensitivity glycomic analysis is essential for advancing both basic and translational biomedical research, yet remains methodologically challenging for limited-quantity samples, primarily due to complex workflows and reliance on specialized instrumentation. Here, we introduce solution-enhanced glycan reduction and permethylation (seGRAP), a streamlined, accessible, and high-sensitive method that enables glycan profiling from sub-nanogram protein inputs and picoliter-scale human plasma using widely available mass spectrometry (MS) platforms. seGRAP-MS demonstrates consistently robust and reproducible glycomic performance and enables comprehensive N-glycome characterization of human oocytes at single-cell resolution. Our single-oocyte analysis uncovers a highly conserved N-glycome across both individuals and developmental stages, revealing a previously uncharacterized layer of molecular stability in human reproduction. By significantly lowering technical and logistical barriers, seGRAP-MS redefines the benchmark for high-sensitive glycomics, expanding accessibility and empowering broader applications in fundamental biology, clinical research, and precision medicine.

Indexed as

GlycomicsMass SpectrometryOocytesPolysaccharidesFemaleHumansSingle-Cell AnalysisPolysaccharides

Identifiers

PMID42399233
PMCPMC13332028

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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 Socratic graph.