Böldicke T, Kindt S, Maywald F, Fitzlaff G, Böcher M, Frank R, Collins J
Department of Genetics, Gesellschaft für Biotechnologische Forschung mbH, Braunschweig, Federal Republic of Germany.
Eur J Biochem. 1988 Aug 1;175(2):259-64. doi: 10.1111/j.1432-1033.1988.tb14191.x.
Specific monoclonal antibodies against the active sites of two genetically engineered pancreatic secretory trypsin inhibitor (PSTI) variants (PSTI 0 and PSTI 4) were produced. The protease inhibitors PSTI 0 and PSTI 4 differ only by three amino acid substitution at their active sites. PSTI 0 inhibits trypsin, whereas PSTI 4 inhibits human granulocyte elastase and chymotrypsin. Immunization was performed in vitro with a synthetic heptapeptide that covers the mutated region of the protein. For this purpose in vitro culture conditions for the production of specific monoclonal antibodies against synthetic peptides were improved. The monoclonal antibodies obtained react specifically with the corresponding protease inhibitor variant. Competition experiments with trypsin and human elastase demonstrate that the protease displace the monoclonal antibody from the active site of PSTI 0 and PSTI 4 respectively.
制备了针对两种基因工程化胰腺分泌型胰蛋白酶抑制剂(PSTI)变体(PSTI 0和PSTI 4)活性位点的特异性单克隆抗体。蛋白酶抑制剂PSTI 0和PSTI 4仅在其活性位点有三个氨基酸取代的差异。PSTI 0抑制胰蛋白酶,而PSTI 4抑制人粒细胞弹性蛋白酶和胰凝乳蛋白酶。用覆盖该蛋白质突变区域的合成七肽在体外进行免疫。为此,改进了用于生产针对合成肽的特异性单克隆抗体的体外培养条件。获得的单克隆抗体与相应的蛋白酶抑制剂变体发生特异性反应。用胰蛋白酶和人弹性蛋白酶进行的竞争实验表明,蛋白酶分别从PSTI 0和PSTI 4的活性位点取代单克隆抗体。