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Protein S



protein S (alpha)
Identifiers
Symbol PROS1
Alt. Symbols PROS
Entrez 5627
HUGO 9456
OMIM 176880
RefSeq NM_000313
UniProt P07225
Other data
Locus Chr. 3 p11-q11.2

Protein S is a vitamin K-dependent plasma glycoprotein synthesized in the liver. In the circulation, Protein S exists in two forms: a free form and a complex form bound to complement protein C4b.

Additional recommended knowledge

Function

The best characterized function of Protein S is its role in the anti coagulation pathway, it functions as a cofactor to Protein C in the inactivation of Factors Va and VIIIa. Only the free form has cofactor activity.

Protein S can bind to negatively charged phospholipids via the carboxylated GLA domain. This property allows Protein S to function in the removal of cells which are undergoing apoptosis. Apoptosis is a form of cell death that is used by the body to remove unwanted or damaged cells from tissues. Cells which are apoptotic (ie. in the process of apoptosis) no longer actively manage the distribution of phospholipids in their outer membrane and hence begin to display negatively charged phospholipids, such as phosphatidyl serine, on the cell surface. In healthy cells, an ATP (Adenosine triphosphate)-dependent enzyme removes these from the outer leaflet of the cell membrane. These negatively charged phospholipids are recognized by phagocytes such as macrophages. Protein S can bind to the negatively charged phospholipids and function as a bridging molecule between the apoptotic cell and the phagocyte. The bridging property of Protein S enhances the phagocytosis of the apoptotic cell, allowing it to be removed 'cleanly' without any symptoms of tissue damage such as inflammation occurring.

Pathology

Protein S deficiency is a rare blood disorder which can lead to an increased risk of thrombosis.

See also

 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Protein_S". A list of authors is available in Wikipedia.
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