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  19F NMR-guided design of glycomimetic Langerin ligands

Wamhoff, E.-C., Hanske, J., Schnirch, L., Aretz, J., Grube, M., Varón Silva, D., et al. (2016). 19F NMR-guided design of glycomimetic Langerin ligands. ACS Chemical Biology, 11(9), 2407-2413. doi:10.1021/acschembio.6b00561.

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Wamhoff, Eike-Christian1, Author           
Hanske, Jonas1, Author           
Schnirch, Lennart, Author
Aretz, Jonas1, Author           
Grube, Maurice2, Author           
Varón Silva, Daniel3, Author           
Rademacher, Christoph1, Author           
Affiliations:
1Christoph Rademacher, Biomolekulare Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863300              
2Daniel Varon-Silva, Biomolekulare Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863302              
3Daniel Varón Silva, Biomolekulare Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863302              

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 Abstract: C-type lectin receptors (CLRs) play a pivotal role in pathogen defense and immune homeostasis. Langerin, a CLR predominantly expressed on Langerhans cells, represents a potential target receptor for the development of anti-infectives or immunomodulatory therapies. As mammalian carbohydrate binding sites typically display high solvent exposure and hydrophilicity, the recognition of natural monosaccharide ligands is characterized by low affinities. Consequently, glycomimetic ligand design poses challenges that extend to the development of suitable assays. Here, we report the first application of 19F R2-filtered NMR to address these challenges for a CLR, i.e., Langerin. The homogeneous, monovalent assay was essential to evaluating the in silico design of 2-deoxy-2-carboxamido-α-mannoside analogs and enabled the implementation of a fragment screening against the carbohydrate binding site. With the identification of both potent monosaccharide analogs and fragment hits, this study represents an important advancement toward the design of glycomimetic Langerin ligands and highlights the importance of assay development for other CLRs.

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 Dates: 2016-07-262016
 Publication Status: Issued
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 Identifiers: DOI: 10.1021/acschembio.6b00561
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Title: ACS Chemical Biology
Source Genre: Journal
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Publ. Info: Washington, D.C. : American Chemical Society
Pages: - Volume / Issue: 11 (9) Sequence Number: - Start / End Page: 2407 - 2413 Identifier: ISSN: 1554-8929