Buttle D J, Murata M, Knight C G, Barrett A J
Department of Biochemistry, Strangeways Research Laboratory, Cambridge, United Kingdom.
Arch Biochem Biophys. 1992 Dec;299(2):377-80. doi: 10.1016/0003-9861(92)90290-d.
The specificity of compound CA074 [N-(L-3-trans-propylcarbamoyloxirane-2-carbonyl)-L-isoleucyl-L-pro line] for the inactivation of cathepsin B was quantified in in vitro measurements with cysteine endopeptidases from cattle, it being found that the compound is a very rapid inactivator of cathepsin B (rate constant 112,000 M-1.s-1), with barely detectable action on cathepsins H, L, and S or m-calpain. Conversion of the proline carboxyl group of the inhibitor to the methyl ester virtually abolished the effect on cathepsin B, and a possible explanation for the importance of the carboxyl is presented on the basis of the tertiary structure of cathepsin B. It was found that CA074 methyl ester (1 microM, 3 h) caused selective inactivation of the intracellular cathepsin B of human gingival fibroblasts in culture, in contrast to other available agents, and we suggest that CA074 methyl ester will be of value in the elucidation of the biological functions of cathepsin B.
通过对牛半胱氨酸内肽酶进行体外测量,定量分析了化合物CA074 [N-(L-3-反式-丙基氨甲酰氧基环氧乙烷-2-羰基)-L-异亮氨酰-L-脯氨酸] 对组织蛋白酶B失活的特异性,发现该化合物是组织蛋白酶B的一种非常快速的失活剂(速率常数为112,000 M-1·s-1),对组织蛋白酶H、L、S或m-钙蛋白酶几乎没有可检测到的作用。将抑制剂的脯氨酸羧基转化为甲酯实际上消除了对组织蛋白酶B的作用,并根据组织蛋白酶B的三级结构对羧基的重要性提出了一种可能的解释。结果发现,与其他现有试剂相比,CA074甲酯(1 μM,3小时)可导致培养的人牙龈成纤维细胞内的组织蛋白酶B发生选择性失活,我们认为CA074甲酯在阐明组织蛋白酶B的生物学功能方面将具有价值。