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Publishing Language: Chinese | Open Access

Detection of glycosylation modification levels based on polymerase chain reaction

Zengqi TAN1( )Huina ZHANG2Lin CAO1
Shaanxi Key Laboratory of Biotechnology and Biochemical Engineering, School of Medicine, Northwest University, Xi’an 710069, China
Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education/College of Life Science, Northwest University, Xi’an 710069, China
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Abstract

Glycosylation is an essential post-translational modification. Over 50% of proteins in the human body undergo glycosylation, which can influence their biological functions and participate in various biological processes. Abnormal glycosylation occurs in a range of physiological and pathological processes, such as cancer, inflammation, or metabolic diseases, making the detection of glycosylation essential. Classical methods for detecting glycosylation, like flow cytometry and mass spectrometry, often struggle with trace-level glycosylation signals. This study reports a DNA amplification-based method for glycan detection. Lectins that recognize and bind certain glycosylations are labeled with single-stranded DNA (ssDNA). The specific binding between lectins and glycans convert the "glycan signal" into a "nucleic acid signal". Using the ssDNA as a template for PCR amplification enables the detection of trace glycosylation signals, offering a new perspective for glycobiology research and the discovery of clinical glycomarker.

CLC number: Q53

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Journal of Northwest University (Natural Science Edition)
Pages 1364-1374

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Cite this article:
TAN Z, ZHANG H, CAO L. Detection of glycosylation modification levels based on polymerase chain reaction. Journal of Northwest University (Natural Science Edition), 2025, 55(6): 1364-1374. https://doi.org/10.16152/j.cnki.xdxbzr.2025-06-014

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Received: 01 September 2025
Published: 25 December 2025
© The Editorial Department of Journal of Northwest University (Natural Science Edition)2025.

This is an open access article under the CC BY-NC-ND 4.0 license (https://creativecommons.org/licenses/by-nc-nd/4.0/).