Pontremoli S, Melloni E, Salamino F, Sparatore B, Michetti M, Horecker B L
Proc Natl Acad Sci U S A. 1984 Jan;81(1):53-6. doi: 10.1073/pnas.81.1.53.
Two neutral Ca2+-dependent proteinases, differing in molecular size, have been isolated from rabbit liver. Both are recovered as inactive proenzymes that can be converted to the active forms by high (0.1-1.0 mM) concentrations of Ca2+ in the absence of substrate or, in the presence of a protein substrate, by low (1-5 microM) concentrations of Ca2+. The activated proteinases required only 1-5 microM Ca2+ for maximal activity. Substrates hydrolyzed were denatured globin, globin, casein, and to a lesser extent, several extracellular proteins; no digestion was observed with several intracellular cytosolic enzymes tested. Only those proteins that served as substrates were capable of promoting conversion of the proenzymes to the active low-Ca2+-requiring proteinases.
已从兔肝脏中分离出两种分子大小不同的中性钙依赖性蛋白酶。两者均以无活性的酶原形式获得,在无底物的情况下,通过高浓度(0.1 - 1.0 mM)的Ca²⁺可将其转化为活性形式;在有蛋白质底物存在时,通过低浓度(1 - 5 μM)的Ca²⁺也可实现转化。活化的蛋白酶最大活性仅需1 - 5 μM Ca²⁺。被水解的底物有变性球蛋白、球蛋白、酪蛋白,以及程度稍轻的几种细胞外蛋白质;在所测试的几种细胞内胞质酶中未观察到消化现象。只有那些作为底物的蛋白质能够促进酶原转化为需要低浓度Ca²⁺的活性蛋白酶。