能夠形成微孔的免疫蛋白“perforin”是消除被病毒感染的細(xì)胞及癌變細(xì)胞所必需的,，由自然殺手及細(xì)胞毒性T-細(xì)胞釋放,。
現(xiàn)在，一種“perforin”單聚物（小鼠perforin R213E）的結(jié)構(gòu)已被確定。對該結(jié)構(gòu)所做分析同時(shí)結(jié)合對低聚孔的一個(gè)冷電子顯微鏡重建結(jié)果表明,，這個(gè)孔內(nèi)的“perforin”單聚物與依賴于膽固醇的溶細(xì)胞素在結(jié)構(gòu)上同源的單聚物相比采用一種“內(nèi)面向外”的取向,。
這種新穎的適應(yīng)性也許可解釋“perforin”是怎樣將支持細(xì)胞凋亡的蛋白酶(granzymes)送入目標(biāo)細(xì)胞中的以及相關(guān)的互補(bǔ)免疫蛋白是怎樣組裝成微孔的。（生物谷Bioon.com）
生物谷推薦英文摘要：
Nature doi:10.1038/nature09518
The structural basis for membrane binding and pore formation by lymphocyte perforin
Ruby H. P. Law,Natalya Lukoyanova,Ilia Voskoboinik,Tom T. Caradoc-Davies,Katherine Baran,Michelle A. Dunstone,Michael E. D’Angelo,Elena V. Orlova,Fasséli Coulibaly,Sandra Verschoor,Kylie A. Browne,Annette Ciccone,Michael J. Kuiper,Phillip I. Bird,Joseph A. Trapani,[email protected] R. Saibil& James C. Whisstock
Natural killer cells and cytotoxic T lymphocytes accomplish the critically important function of killing virus-infected and neoplastic cells. They do this by releasing the pore-forming protein perforin and granzyme proteases from cytoplasmic granules into the cleft formed between the abutting killer and target cell membranes. Perforin, a 67-kilodalton multidomain protein, oligomerizes to form pores that deliver the pro-apoptopic granzymes into the cytosol of the target cell1, 2, 3, 4, 5, 6. The importance of perforin is highlighted by the fatal consequences of congenital perforin deficiency, with more than 50 different perforin mutations linked to familial haemophagocytic lymphohistiocytosis (type 2 FHL)7. Here we elucidate the mechanism of perforin pore formation by determining the X-ray crystal structure of monomeric murine perforin, together with a cryo-electron microscopy reconstruction of the entire perforin pore. Perforin is a thin ‘key-shaped’ molecule, comprising an amino-terminal membrane attack complex perforin-like (MACPF)/cholesterol dependent cytolysin (CDC) domain8, 9 followed by an epidermal growth factor (EGF) domain that, together with the extreme carboxy-terminal sequence, forms a central shelf-like structure. A C-terminal C2 domain mediates initial, Ca2+-dependent membrane binding. Most unexpectedly, however, electron microscopy reveals that the orientation of the perforin MACPF domain in the pore is inside-out relative to the subunit arrangement in CDCs10, 11. These data reveal remarkable flexibility in the mechanism of action of the conserved MACPF/CDC fold and provide new insights into how related immune defence molecules such as complement proteins assemble into pores.
