ArticleBioconjugate chemistry2019
Novel Reversible Fluorescent Glycan Linker for Functional Glycomics.
Article in Bioconjugate chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
What it found
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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.
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Who cites it
9 citing papers in PubMed.
- Versatile Glycan Probes for Multiplatform Investigation of Glycan Interactions with Proteins, Viruses, and Cells.Nature communications · 2026Article
- Article
- Novel Click Coupling Chemistry to Explore Glycan Recognition.ACS central science · 2025Article
- A universal strategy of glyconanoparticle preparation using a bifunctional linker for lectin sensing and cell imaging.Mikrochimica acta · 2022Article
- Regeneration of Free Reducing Glycans from Reductive Amination-Tagged Glycans by Oxone.The Journal of organic chemistry · 2022Article
- The schizophrenia-associated variant in SLC39A8 alters protein glycosylation in the mouse brain.Molecular psychiatry · 2022Article
- Differential recognition of oligomannose isomers by glycan-binding proteins involved in innate and adaptive immunity.Science advances · 2021Article
- Preparation of Complex Glycans From Natural Sources for Functional Study.Frontiers in chemistry · 2020Review
- Glycan Microarrays as Chemical Tools for Identifying Glycan Recognition by Immune Proteins.Frontiers in chemistry · 2019Review
Corrections and comments
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Authors and funding
9 authors.
Funding
Abstract
To aid in generating complex and diverse natural glycan libraries for functional glycomics, more efficient and reliable methods are needed to derivatize glycans. Here we present our development of a reversible, cleavable bifunctional linker 3-(methoxyamino)propylamine (MAPA). As the fluorenylmethyloxycarbonate (Fmoc) version (F-MAPA), it is highly fluorescent and efficiently derivatizes free reducing glycans to generate closed-ring derivatives that preserve the structural integrity of glycans. A library of glycans were derivatized and used to generate a covalent glycan microarray using
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Registered trials
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