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Updated: May 11, 2026

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A Lectin HPLC Method to Enrich Selectively-glycosylated Peptides from Complex Biological Samples
Published on: October 1, 2009
Sugar-attached upconversion lanthanide nanoparticles: a novel tool for high-throughput lectin assay
Yu Liu1, Takuya Kobayashi, Masayuki Iizuka
1Department of Life Science, Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, J2-10, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8501, Japan.
Bioorganic & Medicinal Chemistry
|May 1, 2013
Summary
Researchers developed a novel high-throughput lectin assay (HTPLA) using sugar-coated lanthanide nanoparticles (LNPs). This method detects lectin aggregation via near-infrared light emission, enabling sensitive and specific carbohydrate-binding protein detection.
Area of Science:
- Biochemistry
- Nanotechnology
- Analytical Chemistry
Background:
- Lectins are proteins with diverse biological roles, crucial for cell recognition and adhesion.
- Developing sensitive and high-throughput methods for lectin detection is vital for biological research and diagnostics.
- Current lectin detection methods can be limited in throughput and sensitivity.
Purpose of the Study:
- To develop a novel high-throughput lectin assay (HTPLA) utilizing lanthanide nanoparticles (LNPs).
- To leverage near-infrared (NIR) excitation for sensitive detection of lectin-carbohydrate interactions.
- To demonstrate the specificity and applicability of the assay for lectin characterization.
Main Methods:
- Synthesis of sugar-attached upconversion lanthanide nanoparticles (LNPs).
- Utilizing NIR excitation for luminophore emission detection in aggregated LNPs.
- Employing mannose-coated LNPs for mannose-binding lectin detection.
- Using galactose-coated LNPs for macrophage aggregation assays to assess lectin specificity.
Main Results:
- Significantly enhanced luminophore emission was observed from aggregated mannose-coated LNPs with mannose-binding lectins compared to non-aggregated samples.
- The assay demonstrated high sensitivity, suitable for high-throughput lectin analysis.
- Galactose-coated LNPs successfully facilitated macrophage aggregation assays, confirming lectin sugar-binding specificity.
Conclusions:
- The developed HTPLA method based on NIR-excitable LNPs is sensitive and specific for detecting lectin-carbohydrate interactions.
- This novel assay offers a promising tool for high-throughput screening and characterization of lectins.
- The LNP-based approach provides a versatile platform for studying lectin functions in biological systems.

