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Structure of Bovine CD46 Ectodomain

CD46, or membrane cofactor protein, is a type-one transmembrane protein from the complement regulatory protein family. Alongside its role in complement activation, CD46 is involved in many other processes, from T-cell activation to reproduction. It is also referred to as a pathogen magnet, because i...

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Autores principales: Aitkenhead, Hazel, Stuart, David I., El Omari, Kamel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10385506/
https://www.ncbi.nlm.nih.gov/pubmed/37515111
http://dx.doi.org/10.3390/v15071424
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author Aitkenhead, Hazel
Stuart, David I.
El Omari, Kamel
author_facet Aitkenhead, Hazel
Stuart, David I.
El Omari, Kamel
author_sort Aitkenhead, Hazel
collection PubMed
description CD46, or membrane cofactor protein, is a type-one transmembrane protein from the complement regulatory protein family. Alongside its role in complement activation, CD46 is involved in many other processes, from T-cell activation to reproduction. It is also referred to as a pathogen magnet, because it is used as a receptor by multiple bacteria and viruses. Bovine CD46 (bovCD46) in particular is involved in bovine viral diarrhoea virus entry, an economically important disease in cattle industries. This study presents the X-ray crystallographic structure of the extracellular region of bovCD46, revealing a four-short-consensus-repeat (SCR) structure similar to that in human CD46. SCR1-3 are arranged linearly, while SCR 4 has a reduced interface angle, resulting in a hockey stick-like appearance. The structure also reveals the bovine viral diarrhoea virus interaction site in SCR1, which is likely to confer pestivirus specificity for their target host, CD46. Insights gained from the structural information on pestivirus receptors, such as CD46, could offer valuable guidance for future control strategies.
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spelling pubmed-103855062023-07-30 Structure of Bovine CD46 Ectodomain Aitkenhead, Hazel Stuart, David I. El Omari, Kamel Viruses Article CD46, or membrane cofactor protein, is a type-one transmembrane protein from the complement regulatory protein family. Alongside its role in complement activation, CD46 is involved in many other processes, from T-cell activation to reproduction. It is also referred to as a pathogen magnet, because it is used as a receptor by multiple bacteria and viruses. Bovine CD46 (bovCD46) in particular is involved in bovine viral diarrhoea virus entry, an economically important disease in cattle industries. This study presents the X-ray crystallographic structure of the extracellular region of bovCD46, revealing a four-short-consensus-repeat (SCR) structure similar to that in human CD46. SCR1-3 are arranged linearly, while SCR 4 has a reduced interface angle, resulting in a hockey stick-like appearance. The structure also reveals the bovine viral diarrhoea virus interaction site in SCR1, which is likely to confer pestivirus specificity for their target host, CD46. Insights gained from the structural information on pestivirus receptors, such as CD46, could offer valuable guidance for future control strategies. MDPI 2023-06-23 /pmc/articles/PMC10385506/ /pubmed/37515111 http://dx.doi.org/10.3390/v15071424 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Aitkenhead, Hazel
Stuart, David I.
El Omari, Kamel
Structure of Bovine CD46 Ectodomain
title Structure of Bovine CD46 Ectodomain
title_full Structure of Bovine CD46 Ectodomain
title_fullStr Structure of Bovine CD46 Ectodomain
title_full_unstemmed Structure of Bovine CD46 Ectodomain
title_short Structure of Bovine CD46 Ectodomain
title_sort structure of bovine cd46 ectodomain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10385506/
https://www.ncbi.nlm.nih.gov/pubmed/37515111
http://dx.doi.org/10.3390/v15071424
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