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The arrestins are a family of proteins that are important for regulating signal transduction within cells. Arrestins are part of a conserved two step mechanisms for regulating the activity of G-protein coupled receptors (GPCRs). In response to a stimulus, GPCRs activate a heterotrimeric G protein. In order to turn off this response, or adapt to a constant stimulus, activated receptors need to be silenced. The first step is phosphorylation by a class of serine/threonine kinases called G protein coupled receptor kinases (GRKs). This phosphorylation specifically marks the activated receptor for arrestin binding. Once arrestin is bound to the receptor it is unable to signal further. Recent research continues to expand the known actions of arrestins, which can bind to other classes of receptors and can directly activate signaling pathways on their own.
Additional recommended knowledge
Different arrestins (visual arrestin (or Arrestin 1), beta-arrestin 1 (or Arrestin 2) and beta-arrestin 2 (or Arrestin 3) can reduce the activity of their target GPCRs in several different ways. The simplest mechanism for an arrestin to inhibit the activation of its target is for it to bind to the intracellular domain of the GPCR in such a way that the binding site for the heterotrimeric G-protein is blocked, preventing extra cellular signals from activating the pathway (desensitization). Another regulatory mechanism employed by arrestins is to link the receptor to elements of the membrane internalization machinery (clathrin mediated endocytosis) which leads to the internalization of the receptor in a coated vesicle that is going to fuse to an internal compartment, called endosome. Once in there, the receptor could be either targeted to degradation compartments (lysosomes) or recycled back to the plasma membrane where it will be once again competent for activation.
It has to be noted that at the steady state, beta arrestin is found in the cytoplasm of the cell in an inactive form, characterized by a 'close' 3D conformation. Upon activation and phosphorylation of the GPCR, the protein beta arrestin is recruited at the plasma membrane on the receptor, and activated by a conformational change characterized by a movement of its two globular domains and a released of its C-terminal tail that contains binding sites to the internalization machinery (clathrin, AP-2 complexes). The release of the C-terminal tail leads to the targeting of the beta arrestin/GPCR complexes into clathrin coated pit (internalization structure). The pit is then going to invaginates and finally forms a vesicle that will enter the cytoplasm of the cell. Activation of beta arrestin is crucial as it governs the capacities of the protein to interact with the GPCR and to target the GPCR in clathrin coated pits.
More and more, new functions of beta arrestins are discovered. Recently, it has been shown that beta-arrestin shuttle between nucleus and cytoplasm. The function of beta-arrestin in the nucleus is not yet well understood, even if some data indicate clearly that beta-arrestin enters and exit the nucleus to take out from there some of its partners like the kinase JNK3 or the ubiquitin ligase Mdm2. Those partners have a function in the nucleus, therefore, beta-arrestin, by exporting them outside the nucleus, inhibits their function. In the nucleus, it has also been described that beta arrestins are also able to modify gene expression, by enhancing transcription of some specific genes.
GPCRs form the largest family of receptors, involved in many processes like hormonal system regulation, cardiac regulation, pain, vision, taste, and almost all of them are downregulated by β-Arrestin 1 and/or 2. Beta-arrestin 2, for example, is responsible for the downregulation of β-Adrenergic receptor which is phosphorylated by the β-adrenergic receptor kinase, thyrotropin releasing hormone receptor (TRHR), C5a Receptor (C5aR), AngiotensinII receptor.
It should be noted that arrestins are produced endogenously within lots of cell type, are present in all eukaryotes, therefore conserved among evolution, and do not diffuse across cellular membranes.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Arrestin". A list of authors is available in Wikipedia.|