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A fresh trim provides a new look at the human mannose receptor

The human mannose receptor plays an important role in scavenging a variety of glycans and glycoconjugates, which contributes to both innate and adaptive immunity. However, the fine details of its ligand specificity, and specifically that of carbohydrate-recognition domain 4, the most functionally re...

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Autor principal: Ficko-Blean, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8294574/
https://www.ncbi.nlm.nih.gov/pubmed/34181947
http://dx.doi.org/10.1016/j.jbc.2021.100922
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author Ficko-Blean, Elizabeth
author_facet Ficko-Blean, Elizabeth
author_sort Ficko-Blean, Elizabeth
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description The human mannose receptor plays an important role in scavenging a variety of glycans and glycoconjugates, which contributes to both innate and adaptive immunity. However, the fine details of its ligand specificity, and specifically that of carbohydrate-recognition domain 4, the most functionally relevant C-type lectin domain within the receptor, are not completely understood. Feinberg et al. use glycan arrays, crystallography, and a newly trimmed version of carbohydrate-recognition domain 4 to elucidate the molecular mechanisms driving binding specificity. These data contribute to our molecular understanding of Ca(2+)-mediated binding promiscuity in the human mannose receptor and the scavenging role of the receptor itself and highlight unexpected interactions that should inspire further study.
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spelling pubmed-82945742021-07-23 A fresh trim provides a new look at the human mannose receptor Ficko-Blean, Elizabeth J Biol Chem Editors' Pick Highlight The human mannose receptor plays an important role in scavenging a variety of glycans and glycoconjugates, which contributes to both innate and adaptive immunity. However, the fine details of its ligand specificity, and specifically that of carbohydrate-recognition domain 4, the most functionally relevant C-type lectin domain within the receptor, are not completely understood. Feinberg et al. use glycan arrays, crystallography, and a newly trimmed version of carbohydrate-recognition domain 4 to elucidate the molecular mechanisms driving binding specificity. These data contribute to our molecular understanding of Ca(2+)-mediated binding promiscuity in the human mannose receptor and the scavenging role of the receptor itself and highlight unexpected interactions that should inspire further study. American Society for Biochemistry and Molecular Biology 2021-06-26 /pmc/articles/PMC8294574/ /pubmed/34181947 http://dx.doi.org/10.1016/j.jbc.2021.100922 Text en © 2021 The Author https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Editors' Pick Highlight
Ficko-Blean, Elizabeth
A fresh trim provides a new look at the human mannose receptor
title A fresh trim provides a new look at the human mannose receptor
title_full A fresh trim provides a new look at the human mannose receptor
title_fullStr A fresh trim provides a new look at the human mannose receptor
title_full_unstemmed A fresh trim provides a new look at the human mannose receptor
title_short A fresh trim provides a new look at the human mannose receptor
title_sort fresh trim provides a new look at the human mannose receptor
topic Editors' Pick Highlight
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8294574/
https://www.ncbi.nlm.nih.gov/pubmed/34181947
http://dx.doi.org/10.1016/j.jbc.2021.100922
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