Bures L, Lichý A, Bostík J, Spundová M
Laboratory of Protein Metabolism, Faculty of General Medicine, Charles University, Prague, Czechoslovakia.
Neoplasma. 1990;37(3):225-31.
An alternative method for the preparation of human serum albumin-methotrexate derivative (HSA-MTX) using N-hydroxysuccinimide ester of methotrexate (MTX) was compared with that using the water-soluble carbodiimide (WSC) assistance. The prepared derivative was tested to find the advantages and drawbacks of this method. The N-hydroxysuccinimide ester method is more laborious than that using WSC but some reasons speak in favor of this method. The formation of protein-protein conjugates during the reaction was negligible and under specific conditions more MTX molecules could be bound to protein than by the WSC method. However, some disadvantages of this method were found: A laborious preparation, a small degree of denaturation of protein during the synthesis and, moreover, the binding of MTX to protein did not always take place through NH2-groups of protein but through some other groups (--OH, --SH) as well. These couplings were not so stable as an amidic (or peptidic) bond. In water environment they were hydrolyzed and MTX was slowly released. If there is no difference in a small fraction of protein-protein conjugates, the WSC-assisted method possesses evident advantages over the active MTX ester one, mainly because of the simple preparation of the stable derivative.
将使用甲氨蝶呤(MTX)的N - 羟基琥珀酰亚胺酯制备人血清白蛋白 - 甲氨蝶呤衍生物(HSA - MTX)的替代方法与使用水溶性碳二亚胺(WSC)辅助的方法进行了比较。对制备的衍生物进行测试以找出该方法的优缺点。N - 羟基琥珀酰亚胺酯法比使用WSC的方法更费力,但有些理由支持这种方法。反应过程中蛋白质 - 蛋白质缀合物的形成可忽略不计,并且在特定条件下,与WSC方法相比,更多的MTX分子可以与蛋白质结合。然而,发现该方法存在一些缺点:制备费力,合成过程中蛋白质的变性程度小,而且,MTX与蛋白质的结合并不总是通过蛋白质的NH2基团,也通过一些其他基团( - OH, - SH)。这些偶联不如酰胺(或肽)键稳定。在水环境中它们会水解,MTX会缓慢释放。如果在少量蛋白质 - 蛋白质缀合物方面没有差异,WSC辅助方法相对于活性MTX酯方法具有明显优势,主要是因为稳定衍生物的制备简单。