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The role of the MyD88 intermediate domain in the formation of the myddosome assembly in innate immunity

Dissertation (MSc (Biochemistry))--University of Pretoria, 2023.

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Other Authors: Motshwene, Precious G.
Format: Thesis
Language:English
Published: University of Pretoria 2023
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access_status_str Open Access
author2 Motshwene, Precious G.
author_browse Motshwene, Precious G.
author_facet Motshwene, Precious G.
collection Thesis
dc_rights_str_mv © 2023 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
description Dissertation (MSc (Biochemistry))--University of Pretoria, 2023.
format Thesis
id oai:repository.up.ac.za:2263/93523
institution University of Pretoria (South Africa)
language English
last_indexed 2026-06-10T12:38:37.863Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2023
publishDateRange 2023
publishDateSort 2023
publisher University of Pretoria
publisherStr University of Pretoria
record_format dspace
source_str UPSpace — University of Pretoria Institutional Repository
spelling oai:repository.up.ac.za:2263/93523 The role of the MyD88 intermediate domain in the formation of the myddosome assembly in innate immunity Motshwene, Precious G. u16087713@tuks.co.za Jeranyama, Takudzwa Carlton Mervyn UCTD Myddosome Domain Intermediate Interleukin-1 receptor Protein Innate Immunity Sustainable Development Goals (SDGs) SDG-03: Good health and well-being Natural and agricultural sciences theses SDG-03 Dissertation (MSc (Biochemistry))--University of Pretoria, 2023. Myeloid differentiation primary response protein-88 (MyD88) and Interleukin-1 receptor associated kinase 4 (IRAK-4) are two proteins that are involved in post-receptor signalling in innate immunity. These two proteins have multiple domains. However, they both share a death domain which they use for interacting with each other through homotypic death domain interactions. Although the death domains are essential for the interaction of these two proteins, the MyD88 intermediate domain is also essential for the interaction with IRAK-4. A splice variant of MyD88 that lacks the intermediate domain fails to recruit IRAK-4 during signalling. Death domains of both MyD88 and IRAK-4 interact with each other in vitro to form an undecameric complex known as the Myddosome complex. This complex has a unique stoichiometry of seven MyD88 death domain molecules to four IRAK-4 death domain molecules. It was reconstituted using MyD88 that had both the death and intermediate domains. However, there was a research group that reconstituted the Myddosome without the MyD88 intermediate domain. Their finding was contrary to existing literature. This project set out to investigate the role of the MyD88 intermediate domain in the assembly of the Myddosome complex. We therefore expressed two variants of MyD88 in addition to the IRAK-4 death domain to reconstitute the Myddosome complex. The two variants were the MyD88 death domain and MyD88 that contained both the death and intermediate domains. MyD88 that lacked the intermediate domain was found to be an oligomer using size exclusion chromatography and dynamic light scattering. However, MyD88 that contained only the death domain was monomeric. MyD88 that contained both the death and intermediate domain was mixed with IRAK-4 death domain to reconstitute the Myddosome complex. As expected, we managed to form the Myddosome complex. The presence of this complex was confirmed by size exclusion chromatography and SDS-PAGE. On the contrary, the MyD88 death domain that lacked the intermediate domain failed to form the Myddosome complex when mixed with IRAK-4 death domain. This finding showed that the MyD88 intermediate domain was essential for the Myddosome assembly. It was also in support of existing literature that MyD88 does not interact with IRAK-4 in the absence of its intermediate domain. Biochemistry MSc (Biochemistry) Unrestricted Faculty of Natural and Agricultural Sciences SDG-03:Good heatlh and well-being 2023-11-29T07:28:48Z 2023-11-29T07:28:48Z 2024-04 2023 Dissertation * A2024 http://hdl.handle.net/2263/93523 https://doi.org/10.25403/UPresearchdata.24608430.v1 en © 2023 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria. application/pdf University of Pretoria
spellingShingle UCTD
Myddosome
Domain
Intermediate
Interleukin-1 receptor
Protein
Innate
Immunity
Sustainable Development Goals (SDGs)
SDG-03: Good health and well-being
Natural and agricultural sciences theses SDG-03
The role of the MyD88 intermediate domain in the formation of the myddosome assembly in innate immunity
title The role of the MyD88 intermediate domain in the formation of the myddosome assembly in innate immunity
title_full The role of the MyD88 intermediate domain in the formation of the myddosome assembly in innate immunity
title_fullStr The role of the MyD88 intermediate domain in the formation of the myddosome assembly in innate immunity
title_full_unstemmed The role of the MyD88 intermediate domain in the formation of the myddosome assembly in innate immunity
title_short The role of the MyD88 intermediate domain in the formation of the myddosome assembly in innate immunity
title_sort role of the myd88 intermediate domain in the formation of the myddosome assembly in innate immunity
topic UCTD
Myddosome
Domain
Intermediate
Interleukin-1 receptor
Protein
Innate
Immunity
Sustainable Development Goals (SDGs)
SDG-03: Good health and well-being
Natural and agricultural sciences theses SDG-03
url http://hdl.handle.net/2263/93523
https://doi.org/10.25403/UPresearchdata.24608430.v1