TIRAP: Difference between revisions
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== TIRAP == | |||
[[File:Toll-like_receptor_pathways_revised.jpg|thumb|right|Diagram of Toll-like receptor pathways, including TIRAP involvement.]] | |||
'''TIRAP''' (Toll-interleukin 1 receptor (TIR) domain-containing adaptor protein), also known as '''MAL''' (MyD88-adapter-like), is a critical adaptor protein involved in the signaling pathways of the [[innate immune system]]. It plays a pivotal role in the [[Toll-like receptor]] (TLR) signaling cascade, which is essential for the recognition of [[pathogen-associated molecular patterns]] (PAMPs) and the subsequent activation of [[immune responses]]. | |||
TIRAP is | == Structure == | ||
TIRAP is characterized by the presence of a TIR domain, which is a conserved region found in all members of the TLR family and their associated adaptor proteins. This domain is crucial for protein-protein interactions that facilitate downstream signaling. The TIR domain of TIRAP allows it to interact with other TIR domain-containing proteins, such as [[MyD88]], to propagate the signal initiated by TLR activation. | |||
== | == Function == | ||
TIRAP functions as a bridging adaptor that links specific TLRs to the downstream signaling adaptor MyD88. It is primarily involved in the signaling pathways of TLR2 and TLR4. Upon activation by their respective ligands, TLR2 and TLR4 recruit TIRAP to the plasma membrane, where it facilitates the recruitment of MyD88. This recruitment is essential for the activation of downstream signaling pathways that lead to the production of pro-inflammatory cytokines and type I [[interferons]]. | |||
Mutations in the TIRAP gene have been associated with | == Role in Disease == | ||
Mutations or polymorphisms in the TIRAP gene have been associated with altered susceptibility to various infectious diseases. For example, certain polymorphisms in TIRAP have been linked to increased susceptibility to [[tuberculosis]] and [[malaria]], while others may confer protection against these diseases. The role of TIRAP in inflammatory and autoimmune diseases is also an area of active research, as dysregulation of TLR signaling can contribute to chronic inflammation and autoimmunity. | |||
== | == Related Proteins == | ||
TIRAP is one of several adaptor proteins involved in TLR signaling. Other key adaptors include MyD88, [[TRIF]] (TIR-domain-containing adapter-inducing interferon-_), and [[TRAM]] (TRIF-related adaptor molecule). Each of these adaptors is involved in distinct TLR signaling pathways, contributing to the specificity and diversity of the immune response. | |||
== Related Pages == | |||
* [[Toll-like receptor]] | * [[Toll-like receptor]] | ||
* [[MyD88]] | * [[MyD88]] | ||
* [[Innate immune system]] | * [[Innate immune system]] | ||
* [[ | * [[Pathogen-associated molecular pattern]] | ||
[[Category: | [[Category:Immunology]] | ||
[[Category:Signal transduction]] | [[Category:Signal transduction]] | ||
Latest revision as of 06:19, 16 February 2025
TIRAP[edit]
TIRAP (Toll-interleukin 1 receptor (TIR) domain-containing adaptor protein), also known as MAL (MyD88-adapter-like), is a critical adaptor protein involved in the signaling pathways of the innate immune system. It plays a pivotal role in the Toll-like receptor (TLR) signaling cascade, which is essential for the recognition of pathogen-associated molecular patterns (PAMPs) and the subsequent activation of immune responses.
Structure[edit]
TIRAP is characterized by the presence of a TIR domain, which is a conserved region found in all members of the TLR family and their associated adaptor proteins. This domain is crucial for protein-protein interactions that facilitate downstream signaling. The TIR domain of TIRAP allows it to interact with other TIR domain-containing proteins, such as MyD88, to propagate the signal initiated by TLR activation.
Function[edit]
TIRAP functions as a bridging adaptor that links specific TLRs to the downstream signaling adaptor MyD88. It is primarily involved in the signaling pathways of TLR2 and TLR4. Upon activation by their respective ligands, TLR2 and TLR4 recruit TIRAP to the plasma membrane, where it facilitates the recruitment of MyD88. This recruitment is essential for the activation of downstream signaling pathways that lead to the production of pro-inflammatory cytokines and type I interferons.
Role in Disease[edit]
Mutations or polymorphisms in the TIRAP gene have been associated with altered susceptibility to various infectious diseases. For example, certain polymorphisms in TIRAP have been linked to increased susceptibility to tuberculosis and malaria, while others may confer protection against these diseases. The role of TIRAP in inflammatory and autoimmune diseases is also an area of active research, as dysregulation of TLR signaling can contribute to chronic inflammation and autoimmunity.
Related Proteins[edit]
TIRAP is one of several adaptor proteins involved in TLR signaling. Other key adaptors include MyD88, TRIF (TIR-domain-containing adapter-inducing interferon-_), and TRAM (TRIF-related adaptor molecule). Each of these adaptors is involved in distinct TLR signaling pathways, contributing to the specificity and diversity of the immune response.
