Epsin

Epsins are a family of highly conserved membrane proteins that are important in creating membrane curvature. Epsins contribute to membrane deformations like endocytosis, and block vesicle formation during mitosis. Epsins are a family of highly conserved membrane proteins that are important in creating membrane curvature. Epsins contribute to membrane deformations like endocytosis, and block vesicle formation during mitosis. Epsin contains various protein domains that aid in function. Starting at the N-terminus is the ENTH domain. ENTH stands for Epsin N-Terminal Homolog. The ENTH domain is approximately 150 amino acids long and is highly conserved across species. It is composed of seven α-helices and an eighth helix that is not aligned with the seven helices that make up a superhelical fold. The role of the ENTH domain is to bind membrane lipids which is currently thought to aid in the invagination of the plasma membrane to form clathrin-coated vesicles. Additionally, located toward the C-terminus of the ENTH domain are two to three ubiquitin interacting motifs which aids in ubiquitin dependent recruitment. Following the ENTH domain there is not as much conservation in structure across species. However, in higher eukaryotes there are several conserved motifs such as the clathrin-binding motifs which bind clathrin heavy chain, these motifs flank a cluster of up to eight DP repeats which bind to AP2. In general, most vertebrates contain at least two epsin paralogs. The two paralogs, epsin-1 and epsin-2 are members that contribute to the clathrin coated endocytotic machinery and are localized at the plasma membrane. In mammals, the two main classes of Epsin's are expressed throughout tissues but has the highest expression in the brain, whereas the third Epsin has higher expression in the epidermis and the stomach. Epsins have many different domains to interact with various proteins related to endocytosis. At its N-terminus is an ENTH domain that binds phosphatidylinositol (4,5)-bisphosphate, meaning that it binds a lipid of biological membranes. It has also been postulated that this is a site for cargo-binding. In the middle of the epsin sequence are two UIMs (ubiquitin-interacting motifs). The C-terminus contains multiple binding sites, for example for clathrin and AP2 adaptors. As such, epsins are able to bind to membranes with specific cargo and connect them with the endocytosis machinery, so one may understand epsins as something like Swiss army knives for endocytosis. Epsins may be the major membrane curvature-driving proteins in many clathrin-coated vesicle budding events. In addition to its primary role as an endocytic adapter, there is evidence the epsins play a role in regulating GTPase activity which provides an alternative mechanism for epsin's role in cell polarity and migration. In addition, Epsin is thought to play a role in the Notch Signaling Pathway, which is critical for normal embryonic development. Notch Signaling is dependent on the proteolytic cleavage of the Notch receptor intracellular domain. Epsin's role in Notch Signaling is due to Notch's reliance on ligand endocytosis to release the Notch intracellular domain. This occurs through ubiquitination of the D114 notch ligand which provides a docking location of the epsin UIM domain. Current research suggest that this directing of cargo material aids in the recycling in Notch signaling as well. A study on knock out epsins 1 and 2 in mice showed embryonic death at day 10. Further investigation showed vascular defects in the embryo proper, placenta and yolk sac which are characteristic of a loss in notch signaling. There are four human genes encoding epsin family members, EPN1, EPN2, EPN3, and EPN4. The epsin homologue of C. elegans is EPN-1. EPN-1 conserves the UIM, ENTH domain, and clathrin-binding motif.