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Artikel ; Online: Structural insights into Siglec-15 reveal glycosylation dependency for its interaction with T cells through integrin CD11b.

Lenza, Maria Pia / Egia-Mendikute, Leire / Antoñana-Vildosola, Asier / Soares, Cátia O / Coelho, Helena / Corzana, Francisco / Bosch, Alexandre / Manisha, Prodhi / Quintana, Jon Imanol / Oyenarte, Iker / Unione, Luca / Moure, María Jesús / Azkargorta, Mikel / Atxabal, Unai / Sobczak, Klaudia / Elortza, Felix / Sutherland, James D / Barrio, Rosa / Marcelo, Filipa /
Jiménez-Barbero, Jesús / Palazon, Asis / Ereño-Orbea, June

Nature communications

2023  Band 14, Heft 1, Seite(n) 3496

Abstract: Sialic acid-binding Ig-like lectin 15 (Siglec-15) is an immune modulator and emerging cancer immunotherapy target. However, limited understanding of its structure and mechanism of action restrains the development of drug candidates that unleash its full ... ...

Abstract Sialic acid-binding Ig-like lectin 15 (Siglec-15) is an immune modulator and emerging cancer immunotherapy target. However, limited understanding of its structure and mechanism of action restrains the development of drug candidates that unleash its full therapeutic potential. In this study, we elucidate the crystal structure of Siglec-15 and its binding epitope via co-crystallization with an anti-Siglec-15 blocking antibody. Using saturation transfer-difference nuclear magnetic resonance (STD-NMR) spectroscopy and molecular dynamics simulations, we reveal Siglec-15 binding mode to α(2,3)- and α(2,6)-linked sialic acids and the cancer-associated sialyl-Tn (STn) glycoform. We demonstrate that binding of Siglec-15 to T cells, which lack STn expression, depends on the presence of α(2,3)- and α(2,6)-linked sialoglycans. Furthermore, we identify the leukocyte integrin CD11b as a Siglec-15 binding partner on human T cells. Collectively, our findings provide an integrated understanding of the structural features of Siglec-15 and emphasize glycosylation as a crucial factor in controlling T cell responses.
Mesh-Begriff(e) Humans ; Crystallization ; Epitopes ; Glycosylation ; Integrins ; T-Lymphocytes
Chemische Substanzen Epitopes ; Integrins ; ITGAM protein, human ; SIGLEC15 protein, human
Sprache Englisch
Erscheinungsdatum 2023-06-13
Erscheinungsland England
Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID 2553671-0
ISSN 2041-1723 ; 2041-1723
ISSN (online) 2041-1723
ISSN 2041-1723
DOI 10.1038/s41467-023-39119-8
Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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