Wilson David S, Wu Jiangchun, Peluso Paul, Nock Steffen
Department of Biochemistry, Zyomyx, Inc., 26101 Research Road, Hayward, CA 94545, USA.
J Immunol Methods. 2002 Feb 1;260(1-2):29-36. doi: 10.1016/s0022-1759(01)00514-2.
Pepsinolysis of immunoglobulin (IgG) to yield F(ab')(2) fragments has been utilized for over 40 years, but the most common subclass of mouse immunoglobulin, IgG(1), is resistant to pepsin cleavage. We show here that this resistance is due to N-linked glycosylation. Deglycosylation by peptide: N-glycosidase F (PNGase F) improves pepsinolysis to generate F(ab')(2) fragments for mouse and rat monoclonal IgG(1) and, in some cases, IgG(2b). This effect was observed for antibodies derived from tissue cell culture or ascites fluid, as well as for polyclonal IgGs from mouse serum. As a result of this finding, the preparation of F(ab')(2) fragments from nearly all mouse IgG molecules should now be a robust procedure.
利用胃蛋白酶裂解免疫球蛋白(IgG)以产生F(ab')(2)片段已有40多年历史,但小鼠免疫球蛋白最常见的亚类IgG(1)对胃蛋白酶裂解具有抗性。我们在此表明,这种抗性是由于N-连接糖基化所致。用肽:N-糖苷酶F(PNGase F)进行去糖基化可改善胃蛋白酶裂解,从而为小鼠和大鼠单克隆IgG(1)以及某些情况下的IgG(2b)生成F(ab')(2)片段。对于源自组织细胞培养物或腹水的抗体以及小鼠血清中的多克隆IgG,均观察到了这种效果。基于这一发现,现在从几乎所有小鼠IgG分子制备F(ab')(2)片段应该是一个可靠的方法。