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Nkrp1 Family, from Lectins to Protein Interacting Molecules
The C-type lectin-like receptors include the Nkrp1 protein family that regulates the activity of natural killer (NK) cells. Rat Nkrp1a was reported to bind monosaccharide moieties in a Ca(2+)-dependent manner in preference order of GalNac > GlcNAc >> Fuc >> Gal > Man. These finding...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272133/ https://www.ncbi.nlm.nih.gov/pubmed/25690298 http://dx.doi.org/10.3390/molecules20023463 |
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author | Rozbeský, Daniel Ivanova, Ljubina Hernychová, Lucie Grobárová, Valéria Novák, Petr Černý, Jan |
author_facet | Rozbeský, Daniel Ivanova, Ljubina Hernychová, Lucie Grobárová, Valéria Novák, Petr Černý, Jan |
author_sort | Rozbeský, Daniel |
collection | PubMed |
description | The C-type lectin-like receptors include the Nkrp1 protein family that regulates the activity of natural killer (NK) cells. Rat Nkrp1a was reported to bind monosaccharide moieties in a Ca(2+)-dependent manner in preference order of GalNac > GlcNAc >> Fuc >> Gal > Man. These findings established for rat Nkrp1a have been extrapolated to all additional Nkrp1 receptors and have been supported by numerous studies over the past two decades. However, since 1996 there has been controversy and another article showed lack of interactions with saccharides in 1999. Nevertheless, several high affinity saccharide ligands were synthesized in order to utilize their potential in antitumor therapy. Subsequently, protein ligands were introduced as specific binders for Nkrp1 proteins and three dimensional models of receptor/protein ligand interaction were derived from crystallographic data. Finally, for at least some members of the NK cell C-type lectin-like proteins, the “sweet story” was impaired by two reports in recent years. It has been shown that the rat Nkrp1a and CD69 do not bind saccharide ligands such as GlcNAc, GalNAc, chitotetraose and saccharide derivatives (GlcNAc-PAMAM) do not directly and specifically influence cytotoxic activity of NK cells as it was previously described. |
format | Online Article Text |
id | pubmed-6272133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62721332018-12-13 Nkrp1 Family, from Lectins to Protein Interacting Molecules Rozbeský, Daniel Ivanova, Ljubina Hernychová, Lucie Grobárová, Valéria Novák, Petr Černý, Jan Molecules Review The C-type lectin-like receptors include the Nkrp1 protein family that regulates the activity of natural killer (NK) cells. Rat Nkrp1a was reported to bind monosaccharide moieties in a Ca(2+)-dependent manner in preference order of GalNac > GlcNAc >> Fuc >> Gal > Man. These findings established for rat Nkrp1a have been extrapolated to all additional Nkrp1 receptors and have been supported by numerous studies over the past two decades. However, since 1996 there has been controversy and another article showed lack of interactions with saccharides in 1999. Nevertheless, several high affinity saccharide ligands were synthesized in order to utilize their potential in antitumor therapy. Subsequently, protein ligands were introduced as specific binders for Nkrp1 proteins and three dimensional models of receptor/protein ligand interaction were derived from crystallographic data. Finally, for at least some members of the NK cell C-type lectin-like proteins, the “sweet story” was impaired by two reports in recent years. It has been shown that the rat Nkrp1a and CD69 do not bind saccharide ligands such as GlcNAc, GalNAc, chitotetraose and saccharide derivatives (GlcNAc-PAMAM) do not directly and specifically influence cytotoxic activity of NK cells as it was previously described. MDPI 2015-02-17 /pmc/articles/PMC6272133/ /pubmed/25690298 http://dx.doi.org/10.3390/molecules20023463 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Rozbeský, Daniel Ivanova, Ljubina Hernychová, Lucie Grobárová, Valéria Novák, Petr Černý, Jan Nkrp1 Family, from Lectins to Protein Interacting Molecules |
title | Nkrp1 Family, from Lectins to Protein Interacting Molecules |
title_full | Nkrp1 Family, from Lectins to Protein Interacting Molecules |
title_fullStr | Nkrp1 Family, from Lectins to Protein Interacting Molecules |
title_full_unstemmed | Nkrp1 Family, from Lectins to Protein Interacting Molecules |
title_short | Nkrp1 Family, from Lectins to Protein Interacting Molecules |
title_sort | nkrp1 family, from lectins to protein interacting molecules |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272133/ https://www.ncbi.nlm.nih.gov/pubmed/25690298 http://dx.doi.org/10.3390/molecules20023463 |
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