Guerini D, Krebs J, Carafoli E
J Biol Chem. 1984 Dec 25;259(24):15172-7.
Highly purified tryptic peptides of calmodulin have been obtained by high-performance liquid chromatography. Tryptic cleavage of calmodulin in the presence of Ca2+ results in two main fragments which have been identified by analysis of the amino acid composition as 1-77 and 78-148. In the absence of Ca2+, trypsin cleavage yields fragments 1-106, 1-90, and 107-148. Only fragments 78-148 and 1-106 are still able to stimulate the purified Ca2+-ATPase of erythrocytes, albeit much less efficiently on a molar basis, than intact calmodulin. On the other hand, the same fragments were unable to stimulate the calmodulin-dependent cyclic nucleotide phosphodiesterase, even at 1000-fold molar excess (shown also by Newton, D.L., Oldewurtel, M.D., Krinks, M.H., Shiloach, J., and Klee, C.B. (1984) J. Biol. Chem. 259, 4419-4426). This points to the importance of the carboxyl-terminal half of calmodulin and especially of Ca2+-binding region III in the interaction of calmodulin with the Ca2+-ATPase and provides clear evidence that calmodulin interacts differently with different targets. Oxidation of methionine(s) of fragment 78-148 with N-chlorosuccinimide removes the ability of this fragment to stimulate the ATPase.
通过高效液相色谱法已获得了高度纯化的钙调蛋白胰蛋白酶肽段。在Ca2+存在的情况下,钙调蛋白经胰蛋白酶切割产生两个主要片段,通过氨基酸组成分析确定为1-77和78-148。在没有Ca2+的情况下,胰蛋白酶切割产生片段1-106、1-90和107-148。只有片段78-148和1-106仍能刺激纯化的红细胞Ca2+-ATP酶,尽管以摩尔为基础,其效率远低于完整的钙调蛋白。另一方面,相同的片段甚至在摩尔过量1000倍时也无法刺激钙调蛋白依赖性环核苷酸磷酸二酯酶(牛顿等人(1984年)《生物化学杂志》259卷,4419 - 4426页也有报道)。这表明钙调蛋白羧基末端一半,尤其是Ca2+结合区域III在钙调蛋白与Ca2+-ATP酶相互作用中的重要性,并提供了明确证据,即钙调蛋白与不同靶点的相互作用方式不同。用N-氯代琥珀酰亚胺氧化片段78-148的甲硫氨酸会消除该片段刺激ATP酶的能力。