Decoding of Carbohydrates With Monosaccharide‐Level Resolution Using Tip‐Enhanced Raman Scattering

We report a tip-enhanced Raman spectroscopy (TERS) platform integrated with nanopillar-assisted glycan trapping for high-sensitivity, label-free analysis of oligosaccharides. Mechanical confinement of glycans generates localized plasmonic hot spots, enabling highly reproducible and structurally informative vibrational spectra. The system resolves subtle structural differences such as β(1→3) vs. β(1→4) glycosidic linkages, and allows semi-quantitative estimation of chain length based on H-C-H deformation signatures. The azido tag provides an internal reference, supporting signal normalization from trace sample volumes. The platform also tracks enzymatic glycosylation reactions in real time, including the emergence of α1→2 fucosylation linkages. This approach distinguishes single-bond differences and monitors biosynthetic progression with high molecular specificity. This work establishes TERS as a powerful tool for glycan sequence analysis and dynamic monitoring of carbohydrate synthesis.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2026-03-13
DOI
https://doi.org/10.1002/anie.202520019
Primary Topic
Glycosylation and Glycoproteins Research
Type
article
Field-Weighted Citation Impact
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article

Decoding of Carbohydrates With Monosaccharide‐Level Resolution Using Tip‐Enhanced Raman Scattering

Jia‐Lin Fang, Kien Voon Kong, Chin‐Yu Liang, Teng‐Wei Tsai et al.
Angewandte Chemie International Edition
Glycosylation and Glycoproteins Research
article

Decoding of Carbohydrates With Monosaccharide‐Level Resolution Using Tip‐Enhanced Raman Scattering

Jia‐Lin Fang, Kien Voon Kong, Chin‐Yu Liang, Teng‐Wei Tsai, Chia-Mu Yu, R. FAN, Po‐Chiao Lin, Hsiang‐En Chen
article en

Abstract

We report a tip-enhanced Raman spectroscopy (TERS) platform integrated with nanopillar-assisted glycan trapping for high-sensitivity, label-free analysis of oligosaccharides. Mechanical confinement of glycans generates localized plasmonic hot spots, enabling highly reproducible and structurally informative vibrational spectra. The system resolves subtle structural differences such as β(1→3) vs. β(1→4) glycosidic linkages, and allows semi-quantitative estimation of chain length based on H-C-H deformation signatures. The azido tag provides an internal reference, supporting signal normalization from trace sample volumes. The platform also tracks enzymatic glycosylation reactions in real time, including the emergence of α1→2 fucosylation linkages. This approach distinguishes single-bond differences and monitors biosynthetic progression with high molecular specificity. This work establishes TERS as a powerful tool for glycan sequence analysis and dynamic monitoring of carbohydrate synthesis.

Angewandte Chemie International Edition
National Sun Yat-sen University (TW), National Chung Cheng University (TW), Kaohsiung Medical University (TW), National Taiwan University (TW), National Tsing Hua University (TW), Institute of Biological Chemistry, Academia Sinica (TW)
Openalex Percentile: Top 23%
Glycosylation and Glycoproteins Research
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