Poznansky M J
Appl Biochem Biotechnol. 1984;10:41-56. doi: 10.1007/BF02783734.
The widespread use of enzymes as drugs or therapeutic agents has been limited by (a) enzyme availability, (b) biodegradation of administered enzyme, (c) immunogenecity of the enzyme as a foreign protein, and (d) accessibility of the enzyme to the appropriate site of action. It has become obvious that due to these limitations, the administration of free or native enzyme is not likely to be effective. Various mechanisms of protecting or packaging enzymes to offset some of these drawbacks have been described. We have been successful in producing conjugates of a number of different enzymes with a molar excess of homologous albumin. The resulting enzyme-albumin complex is resistant to proteolytic and heat inactivation and is apparently non-immunogenic. Using specific ligands crosslinked to the enzyme-albumin conjugate we have been able to target these conjugates to specific receptor sites and specific tissues. Ligands including cell surface-recognizing antibodies and hormones such as insulin have been used. These approaches offer new possibilities for the increased use of enzymes in medicine.
(a) 酶的可获得性;(b) 给药酶的生物降解;(c) 酶作为外来蛋白质的免疫原性;以及 (d) 酶到达适当作用部位的可及性。显而易见,由于这些限制,游离或天然酶的给药不太可能有效。已经描述了多种保护或包装酶以抵消其中一些缺点的机制。我们成功地制备了多种不同酶与摩尔过量的同源白蛋白的缀合物。所得的酶 - 白蛋白复合物对蛋白水解和热失活具有抗性,并且显然无免疫原性。通过使用与酶 - 白蛋白缀合物交联的特异性配体,我们能够将这些缀合物靶向特定的受体位点和特定组织。已使用包括细胞表面识别抗体和胰岛素等激素在内的配体。这些方法为酶在医学中的更多应用提供了新的可能性。