Dupont Didier, Rolet-Repecaud Odile, Senocq Daniel
INRA, Unité de Recherches en Technologie et Analyses Laitières, B.P. 89 F-39801 Poligny Cedex, France.
Anal Biochem. 2003 Jun 15;317(2):240-6. doi: 10.1016/s0003-2697(03)00115-5.
Proteolysis is a generic biochemical process that is central in all biological activities. A new strategy for monitoring this biochemical process is proposed here. This approach is based on the production of rabbit polyclonal anti-peptide antibodies directly against the cleavage site on the substrate of the enzyme responsible for proteolysis. So long as the molecule's cleavage site is intact, the antibody will bind to the protein. However, after cleavage of the peptide bond by the protease, the antibody will no longer be able to recognize the substrate. Thus, the development of an ELISA that uses this specific antibody allows hydrolysis of the substrate protein to be monitored. Hydrolysis of beta-casein by plasmin, the main indigenous protease of milk, during the ripening of Swiss-type cheese, has been chosen as a model for this study.
蛋白质水解是一种普遍存在的生化过程,在所有生物活动中都起着核心作用。本文提出了一种监测这一生化过程的新策略。该方法基于直接针对负责蛋白质水解的酶的底物上的切割位点产生兔多克隆抗肽抗体。只要分子的切割位点保持完整,抗体就会与蛋白质结合。然而,在蛋白酶切割肽键后,抗体将不再能够识别底物。因此,开发一种使用这种特异性抗体的酶联免疫吸附测定(ELISA)可以监测底物蛋白的水解情况。在瑞士型奶酪成熟过程中,用纤溶酶(牛奶的主要内源蛋白酶)水解β-酪蛋白已被选作本研究的模型。