
[PERFOR(ATE) + -IN.]
| percutaneous, perchloric acid, percentage | |
| performic acid, perfusate, perfuse |
A protein in cytotoxic T lymphocytes that creates transmembrane pores that act as ion channels in the target cell. Structurally and chemically related to C9 protein of complement which performs a similar function.
Perforin-1 is a protein that in humans is encoded by the PRF1 gene.[2][3][4]
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Perforin is a cytolytic protein found in the granules of Cytotoxic T lymphocytes (CTLs) and NK cells. Upon degranulation, perforin inserts itself into the target cell's plasma membrane, forming a pore. The lytic membrane-inserting part of perforin is the MACPF domain.[5] This region shares homology with cholesterol-dependent cytolysins from Gram-positive bacteria.[1]
Perforin has structural and functional similarities to complement component 9 (C9). Like C9, this protein creates transmembrane tubules and is capable of lysing non-specifically a variety of target cells. This protein is one of the main cytolytic proteins of cytolytic granules, and it is known to be a key effector molecule for T-cell- and natural killer-cell-mediated cytolysis.[4]
Defects in this gene cause familial hemophagocytic lymphohistiocytosis type 2 (HPLH2), a rare and lethal autosomal recessive disorder of early childhood.[4]
Perforin has been shown to interact with Calreticulin.[6]
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Perforin at NLM Genetics Home Reference
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