Kolb G, Köppler H, Gramse M, Havemann K
Immunobiology. 1982 May;161(5):507-23. doi: 10.1016/S0171-2985(82)80053-3.
The elastase-like protease (ELP) from human polymorphonuclear granulocytes (PNM) is able to split human IgG into Fab and Fc-like fragments and smaller peptides. These fragments are similar but not identical to those produced by papain. They differ in their electrophoretical mobility as well as in their molecular weights. Both ELP-Fab and papain-Fab show antigen-binding capacity. In contrast to papain-derived split products of IgG, the ELP-generated Fab and Fc fragments could enhance granulocyte function. Both ELP-Fab and ELP-Fc increase the spontaneous reduction of nitroblue-tetrazolium (NBT) in granulocytes dose-dependent in a homologous as well as in an autologous system. Furthermore, the ELP-derived Fab and Fc induce an active release of ELP by PMN. It could also be demonstrated that Fab as well as Fc increased the peroxidase activity in granulocytes.
来自人多形核粒细胞(PNM)的类弹性蛋白酶蛋白酶(ELP)能够将人IgG裂解为Fab和Fc样片段以及更小的肽段。这些片段与木瓜蛋白酶产生的片段相似但并不相同。它们在电泳迁移率和分子量方面存在差异。ELP-Fab和木瓜蛋白酶-Fab均表现出抗原结合能力。与木瓜蛋白酶衍生的IgG裂解产物不同,ELP产生的Fab和Fc片段可增强粒细胞功能。ELP-Fab和ELP-Fc在同源和自体系统中均以剂量依赖性方式增加粒细胞中硝基蓝四唑(NBT)的自发还原。此外,ELP衍生的Fab和Fc可诱导PMN主动释放ELP。还可以证明Fab以及Fc均可增加粒细胞中的过氧化物酶活性。