Rousseaux J, Rousseaux-Prévost R, Bazin H
J Immunol Methods. 1983 Nov 11;64(1-2):141-6. doi: 10.1016/0022-1759(83)90392-7.
The optimal conditions for the preparation of Fab and F(ab')2 fragments from monoclonal rat IgG of different subclasses are described. Digestion of IgG for 2-4 h at 37 degrees C with 1% (w/w) papaïn at pH 7.0 in the presence of 0.01 M cysteine leads to almost complete cleavage into Fab and Fc fragments. Fab fragments are isolated by sequential chromatography on Ultrogel AcA 44 and on DEAE-cellulose columns. In the case of IgG2c subclass, Fab fragment may be directly isolated by chromatography on Protein A-Sepharose. Production of F(ab')2 fragments from rat IgG1 and IgG2a is obtained with best yield by treatment at acid pH (pH 2.8) before incubation with 1% (w/w) pepsin at pH 4.5 for 4 h at 37 degrees C. For monoclonal IgG2b the best procedure is incubation with S. aureus V8 protease at pH 7.8 (4 h at 37 degrees C with an E/S ratio of 1/30 (w/w]. The best yield of F(ab')2 from monoclonal IgG2c is obtained by incubation for 4 h at 37 degrees C with 1% (w/w) pepsin. F(ab')2 fragments (or the F(ab)2-like fragment released by digestion of IgG2b with S. aureus V8 protease) are isolated by gel filtration on Ultrogel AcA 44.
本文描述了从不同亚类的大鼠单克隆IgG制备Fab和F(ab')2片段的最佳条件。在0.01M半胱氨酸存在下,于pH 7.0用1%(w/w)木瓜蛋白酶在37℃将IgG消化2 - 4小时,几乎可完全裂解为Fab和Fc片段。通过先后在Ultrogel AcA 44和DEAE - 纤维素柱上进行层析分离Fab片段。对于IgG2c亚类,Fab片段可通过在蛋白A - 琼脂糖上进行层析直接分离。大鼠IgG1和IgG2a的F(ab')2片段通过在酸性pH(pH 2.8)下处理,然后于pH 4.5用1%(w/w)胃蛋白酶在37℃孵育4小时,可获得最佳产率。对于单克隆IgG2b,最佳方法是在pH 7.8下与金黄色葡萄球菌V8蛋白酶孵育(在37℃以1/30(w/w)的酶/底物比例孵育4小时)。单克隆IgG2c的F(ab')2最佳产率是通过在37℃用1%(w/w)胃蛋白酶孵育4小时获得。F(ab')2片段(或用金黄色葡萄球菌V8蛋白酶消化IgG2b释放出的类似F(ab)2的片段)通过在Ultrogel AcA 44上进行凝胶过滤分离。