Imperial College London

DrTeresaThurston

Faculty of MedicineDepartment of Infectious Disease

Senior Lecturer in Molecular Microbiology
 
 
 
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Contact

 

+44 (0)20 7594 3072t.thurston

 
 
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Location

 

2.40Flowers buildingSouth Kensington Campus

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Summary

 

Publications

Citation

BibTex format

@article{Thurston:2021:10.3389/fimmu.2021.697588,
author = {Thurston, T and Rajpoot, S and Wary, K and Ibbott, R and Liu, D and Saqib, U and Baig, M},
doi = {10.3389/fimmu.2021.697588},
journal = {Frontiers in Immunology},
pages = {1--12},
title = {TIRAP in the mechanism of inflammation},
url = {http://dx.doi.org/10.3389/fimmu.2021.697588},
volume = {12},
year = {2021}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - The Toll-interleukin-1 Receptor (TIR) domain-containing adaptor protein (TIRAP) represents a key intracellular signalling molecule regulating diverse immune responses. Its capacity to function as an adaptor molecule has been widely investigated in relation to Toll-like Receptor (TLR)-mediated innate immune signalling. Since the discovery of TIRAP in 2001, initial studies were mainly focused on its role as an adaptor protein that couples Myeloid differentiation factor 88 (MyD88) with TLRs, to activate MyD88-dependent TLRs signalling. Subsequent studies delineated TIRAP’s role as a transducer of signalling events through its interaction with non-TLR signalling mediators. Indeed, the ability of TIRAP to interact with an array of intracellular signalling mediators suggests its central role in various immune responses. Therefore, continued studies that elucidate the molecular basis of various TIRAP-protein interactions and how they affect the signalling magnitude, should provide key information on the inflammatory disease mechanisms. This review summarizes the TIRAP recruitment to activated receptors and discusses the mechanism of interactions in relation to the signalling that precede acute and chronic inflammatory diseases. Furthermore, we highlighted the significance of TIRAP-TIR domain containing binding sites for several intracellular inflammatory signalling molecules. Collectively, we discuss the importance of the TIR domain in TIRAP as a key interface involved in protein interactions which could hence serve as a therapeutic target to dampen the extent of acute and chronic inflammatory conditions.
AU - Thurston,T
AU - Rajpoot,S
AU - Wary,K
AU - Ibbott,R
AU - Liu,D
AU - Saqib,U
AU - Baig,M
DO - 10.3389/fimmu.2021.697588
EP - 12
PY - 2021///
SN - 1664-3224
SP - 1
TI - TIRAP in the mechanism of inflammation
T2 - Frontiers in Immunology
UR - http://dx.doi.org/10.3389/fimmu.2021.697588
UR - https://www.frontiersin.org/articles/10.3389/fimmu.2021.697588/full
UR - http://hdl.handle.net/10044/1/90626
VL - 12
ER -