Deistung J, Forde D M, O'Connell J P, Proudfoot K A, Eaton D, Willenbrock F, Kingaby R O, Hughes B, Angal S, Catterall C
Celltech Limited, Slough, Berks, U.K.
J Chromatogr. 1991 Feb 22;539(2):485-92. doi: 10.1016/s0021-9673(01)83958-3.
Recombinant DNA technology has been employed to produce a hybrid gene in which the kringle and serine protease domains of tissue plasminogen activator are linked to the heavy-chain Fd region of a fibrin-specific antibody. The hybrid gene is co-expressed with antibody light chains. This communication describes a purification procedure for the hybrid protein, involving affinity and ion-exchange chromatography. The purified hybrid protein has been used in vivo and in vitro clot lysis experiments and has been shown to be effective at clot dissolution.
重组DNA技术已被用于产生一种杂交基因,其中组织纤溶酶原激活物的kringle和丝氨酸蛋白酶结构域与纤维蛋白特异性抗体的重链Fd区域相连。该杂交基因与抗体轻链共表达。本通讯描述了一种用于该杂交蛋白的纯化程序,包括亲和色谱和离子交换色谱。纯化后的杂交蛋白已用于体内和体外的凝块溶解实验,并已证明在溶解凝块方面有效。