View source for Receptor Tyrosine Kinases in Cell Signaling

==Introduction==

Receptor tyrosine kinases (RTKs) are a class of [[Enzyme|enzymes]] that play a crucial role in cellular communication and regulation. These enzymes are part of the larger family of [[Protein Kinase|protein kinases]], which are responsible for the addition of phosphate groups to proteins, a process known as phosphorylation. RTKs are unique in that they are activated by the binding of specific [[Ligand (biochemistry)|ligands]], leading to a cascade of intracellular events that ultimately result in changes in cell behavior.

[[Image:Detail-39695.jpg|thumb|center|A close-up view of a receptor tyrosine kinase embedded in a cell membrane, with a ligand binding to it.|class=only_on_mobile]]
[[Image:Detail-39696.jpg|thumb|center|A close-up view of a receptor tyrosine kinase embedded in a cell membrane, with a ligand binding to it.|class=only_on_desktop]]

==Structure and Function==

RTKs are transmembrane proteins, meaning they span the entire width of the cell membrane. They consist of an extracellular ligand-binding domain, a single transmembrane helix, and an intracellular kinase domain. The ligand-binding domain is responsible for recognizing and binding to specific ligands, while the kinase domain carries out the phosphorylation of tyrosine residues on specific target proteins.

==Activation and Signal Transduction==

The activation of RTKs begins with the binding of a ligand to the extracellular domain. This binding induces a conformational change in the RTK, causing two RTK molecules to come together in a process known as dimerization. Dimerization activates the kinase domain, which then phosphorylates tyrosine residues on the intracellular portion of the RTK. These phosphorylated residues serve as docking sites for proteins containing Src homology 2 (SH2) and phosphotyrosine-binding (PTB) domains, initiating a series of downstream signaling events.

==Downstream Signaling Pathways==

There are several major signaling pathways activated by RTKs, including the MAPK/ERK pathway, the PI3K/Akt pathway, and the JAK/STAT pathway. Each of these pathways is responsible for regulating different aspects of cell behavior.

===MAPK/ERK Pathway===

The [[Mitogen-activated protein kinase|MAPK/ERK]] pathway is involved in the regulation of cell proliferation, differentiation, and survival. Activation of this pathway begins with the recruitment of the adaptor protein Grb2 and the guanine nucleotide exchange factor SOS to the phosphorylated RTK. This leads to the activation of the protein Ras, which in turn activates a series of kinases culminating in the activation of MAPK/ERK.

===PI3K/Akt Pathway===

The [[Phosphoinositide 3-kinase|PI3K/Akt]] pathway is involved in the regulation of cell survival and growth. Activation of this pathway begins with the recruitment of PI3K to the phosphorylated RTK. PI3K then generates phosphatidylinositol-3,4,5-trisphosphate (PIP3), a second messenger that recruits and activates Akt.

===JAK/STAT Pathway===

The [[Janus kinase|JAK/STAT]] pathway is involved in the regulation of gene expression and cell proliferation. Activation of this pathway begins with the recruitment of JAK to the phosphorylated RTK. JAK then phosphorylates and activates STAT, which translocates to the nucleus and regulates gene expression.

==Regulation of RTK Activity==

The activity of RTKs is tightly regulated to prevent inappropriate cell signaling. One mechanism of regulation is through the action of protein tyrosine phosphatases (PTPs), which remove phosphate groups from tyrosine residues, effectively turning off RTK signaling. Another mechanism is through the action of ubiquitin ligases, which mark RTKs for degradation by the proteasome.

==Role in Disease==

Dysregulation of RTK signaling can lead to a variety of diseases, including cancer. Mutations that lead to the overexpression or constitutive activation of RTKs can result in uncontrolled cell proliferation and survival, hallmarks of cancer. In addition, mutations that impair the function of PTPs or ubiquitin ligases can also lead to dysregulated RTK signaling and disease.

==See Also==
* [[Protein Kinase]]
* [[Ligand (biochemistry)]]
* [[Mitogen-activated protein kinase]]
* [[Phosphoinositide 3-kinase]]
* [[Janus kinase]]

[[Category:Cell biology]]
[[Category:Molecular biology]]
[[Category:Signal transduction]]
[[Category:random]]