Direct derivatization of sialic acids and mild β-elimination for linkage-specific sialyl O-glycan analysis.

Derivatization Glycosidic linkage Mass spectrometry O-Glycan Sialic acid β-Elimination

Journal

Analytica chimica acta
ISSN: 1873-4324
Titre abrégé: Anal Chim Acta
Pays: Netherlands
ID NLM: 0370534

Informations de publication

Date de publication:
22 Aug 2024
Historique:
received: 13 04 2024
revised: 03 07 2024
accepted: 04 07 2024
medline: 28 7 2024
pubmed: 28 7 2024
entrez: 27 7 2024
Statut: ppublish

Résumé

In sharp contrast with analysis of N-glycan that can be prepared by PNGase F, O-glycan analysis remains challenging due to a lack of versatile and simple procedures, especially those mediating cleavage of O-glycans from proteins. Most N-glycans and O-glycans are modified with sialic acids at the non-reducing end and their glycosidic linkages are labile, making it difficult to measure glycans by mass spectrometric analysis. In addition, sialic acid residues present on glycan chains via α2,3-, α2,6-, and α2,8-linkages as structural isomers. In this study, we firstly established a direct and linkage-specific derivatization method for sialylated O-glycans on proteins via linkage-specific lactone-opening aminolysis. In this procedure, labile sialylated glycans were not only stabilized, but also allowed distinguishing between sialyl linkages. Furthermore, we revealed that general reductive β-elimination was not useful for O-glycan cleavages with undesirable degradations of resulting methyl amides. Using β-elimination in the presence of pyrazolone (PMP), with low pH despite alkali base concentration, SALSA-derivatized O-glycans could be cleaved with minimal degradations. Cleaved and PMP-labeled O-glycans could be efficiently prepared in an open reaction system at high temperature (evaporative BEP reaction) and detected by simple liquid-phase extraction. Moreover, in the evaporative BEP reaction by changing the alkali solution with LiOH, the lithiated O-glycans could be observed and provided a lot of fragment information reflecting the complex structure of the O-glycans. Direct sialic acid linkage-specific derivatization of O-glycans on glycoproteins is simple protocol containing in-solution aminolysis-SALSA and acetonitrile precipitation for removal of excess reagents. Evaporative β-elimination with pyrazolone makes possible intact O-linked glycan analysis just by liquid-phase extraction. These analytical methods established by the appropriate combination of direct-SALSA and evaporative β-elimination will facilitate O-glycomic studies in various biological samples.

Sections du résumé

BACKGROUND BACKGROUND
In sharp contrast with analysis of N-glycan that can be prepared by PNGase F, O-glycan analysis remains challenging due to a lack of versatile and simple procedures, especially those mediating cleavage of O-glycans from proteins. Most N-glycans and O-glycans are modified with sialic acids at the non-reducing end and their glycosidic linkages are labile, making it difficult to measure glycans by mass spectrometric analysis. In addition, sialic acid residues present on glycan chains via α2,3-, α2,6-, and α2,8-linkages as structural isomers.
RESULTS RESULTS
In this study, we firstly established a direct and linkage-specific derivatization method for sialylated O-glycans on proteins via linkage-specific lactone-opening aminolysis. In this procedure, labile sialylated glycans were not only stabilized, but also allowed distinguishing between sialyl linkages. Furthermore, we revealed that general reductive β-elimination was not useful for O-glycan cleavages with undesirable degradations of resulting methyl amides. Using β-elimination in the presence of pyrazolone (PMP), with low pH despite alkali base concentration, SALSA-derivatized O-glycans could be cleaved with minimal degradations. Cleaved and PMP-labeled O-glycans could be efficiently prepared in an open reaction system at high temperature (evaporative BEP reaction) and detected by simple liquid-phase extraction. Moreover, in the evaporative BEP reaction by changing the alkali solution with LiOH, the lithiated O-glycans could be observed and provided a lot of fragment information reflecting the complex structure of the O-glycans.
SIGNIFICANCE CONCLUSIONS
Direct sialic acid linkage-specific derivatization of O-glycans on glycoproteins is simple protocol containing in-solution aminolysis-SALSA and acetonitrile precipitation for removal of excess reagents. Evaporative β-elimination with pyrazolone makes possible intact O-linked glycan analysis just by liquid-phase extraction. These analytical methods established by the appropriate combination of direct-SALSA and evaporative β-elimination will facilitate O-glycomic studies in various biological samples.

Identifiants

pubmed: 39067924
pii: S0003-2670(24)00746-3
doi: 10.1016/j.aca.2024.342945
pii:
doi:

Substances chimiques

Polysaccharides 0
Sialic Acids 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

342945

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Hisatoshi Hanamatsu (H)

Institute for Glyco-core Research (iGCORE), Nagoya University, Nagoya, 464-8601, Japan.

Ikuko Yokota (I)

Institute for Glyco-core Research (iGCORE), Nagoya University, Nagoya, 464-8601, Japan.

Masaki Kurogochi (M)

Institute for Glyco-core Research (iGCORE), Nagoya University, Nagoya, 464-8601, Japan; Laboratory of Glyco-Organic Chemistry, The Noguchi Institute, Tokyo, 173-0003, Japan.

Keiko Akasaka-Manya (K)

Molecular Glycobiology, Research Team for Mechanism of Aging, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, 173-0015, Japan.

Nobuaki Miura (N)

Institute for Glyco-core Research (iGCORE), Nagoya University, Nagoya, 464-8601, Japan.

Hiroshi Manya (H)

Molecular Glycobiology, Research Team for Mechanism of Aging, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, 173-0015, Japan.

Tamao Endo (T)

Molecular Glycobiology, Research Team for Mechanism of Aging, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, 173-0015, Japan.

Takashi Nishikaze (T)

Solutions COE, Analytical & Measuring Instruments Division, Shimadzu Corporation, Kyoto, 604-8511, Japan. Electronic address: nishikaz@shimadzu.co.jp.

Jun-Ichi Furukawa (JI)

Institute for Glyco-core Research (iGCORE), Nagoya University, Nagoya, 464-8601, Japan; Department of Orthopaedic Surgery, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, 060-8638, Japan. Electronic address: furukawa.junichi.n0@f.mail.nagoya-u.ac.jp.

Koichi Tanaka (K)

Koichi Tanaka Mass Spectrometry Research Laboratory, Shimadzu Corporation, Kyoto, 604-8511, Japan.

Articles similaires

Animals Flax Chickens Dietary Supplements Endo-1,4-beta Xylanases
Xylitol Zea mays Polysaccharides Xylose Candida tropicalis
Humans Breast Neoplasms Female Fatigue Chemotherapy, Adjuvant
Lignin Genome, Fungal Laccase Peroxidases Fungal Proteins

Classifications MeSH