Unprecedented selectivity for homologous lectin targets: differential targeting of the viral receptors L-SIGN and DC-SIGN

Author:

Delaunay Clara1,Pollastri Sara2ORCID,Thépaut Michel1,Cavazzoli Gianluca2,Belvisi Laura2ORCID,Bouchikri Clémentine1,Labiod Nuria3,Lasala Fatima3,Gimeno Ana4,Franconetti Antonio4ORCID,Jiménez-Barbero Jesús456ORCID,Ardá Ana45,Delgado Rafael37,Bernardi Anna2ORCID,Fieschi Franck18ORCID

Affiliation:

1. Université Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale, Grenoble, France

2. Università degli Studi di Milano, Dipartimento di Chimica, via Golgi 19, Milano, Italy

3. Instituto de Investigacion Hospital Universitario 12 de Octubre, Universidad Complutense, School of Medicine, Madrid, Spain

4. Chemical Glycobiology Lab, Center for Cooperative Research in Biosciences (CIC bioGUNE), Basque Research and Technology Alliance (BRTA), 48160 Derio, Bizkaia, Spain

5. Ikerbasque, Basque Foundation for Science, Bilbao, Spain

6. Centro de Investigacion Biomedica En Red de Enfermedades Respiratorias, 28029 Madrid, Spain

7. School of Medicine, Universidad Complutense, Madrid, Spain

8. Institut Universitaire de France (IUF), Paris, France

Abstract

DC-SIGN and L-SIGN are C-type lectin receptors that act as viral coreceptors for SARS-CoV-2. Their distinct tissue localization justifies the search for a selective ligand for L-SIGN, despite their high homology suggesting the task hard to achieve.

Funder

French Infrastructure for Integrated Structural Biology

Agence Nationale de la Recherche

Comunidad de Madrid

Instituto de Salud Carlos III

Publisher

Royal Society of Chemistry (RSC)

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