Goll D E, Thompson V F, Taylor R G, Zalewska T
Muscle Biology Group, University of Arizona, Tucson 85721.
Bioessays. 1992 Aug;14(8):549-56. doi: 10.1002/bies.950140810.
Although the Ca(2+)-dependent proteinase (calpain) system has been found in every vertebrate cell that has been examined for its presence and has been detected in Drosophila and parasites, the physiological function(s) of this system remains unclear. Calpain activity has been associated with cleavages that alter regulation of various enzyme activities, with remodeling or disassembly of the cell cytoskeleton, and with cleavages of hormone receptors. The mechanism regulating activity of the calpain system in vivo also is unknown. It has been proposed that binding of the calpains to phospholipid in a cell membrane lowers the Ca2+ concentration, [Ca2+], required for the calpains to autolyze, and that autolysis converts an inactive proenzyme into an active protease. Recent studies, however, show that the calpains bind to specific proteins and not to phospholipids, and that binding to cell membranes does not affect the [Ca2+] required for autolysis. It seems likely that calpain activity is regulated by binding of Ca2+ to specific sites on the calpain molecule, with binding to each site eliciting a response (proteolytic activity, calpastatin binding, etc.) specific for that site. Regulation must also involve an, as yet, undiscovered mechanism that increases the affinity of the Ca(2+)-binding sites for Ca2+.
尽管在每一个接受过检查的脊椎动物细胞中都发现了依赖钙离子的蛋白酶(钙蛋白酶)系统,并且在果蝇和寄生虫中也检测到了该系统,但其生理功能仍不清楚。钙蛋白酶活性与改变各种酶活性调控的裂解作用、细胞细胞骨架的重塑或解体以及激素受体的裂解有关。体内调节钙蛋白酶系统活性的机制也尚不清楚。有人提出,钙蛋白酶与细胞膜中的磷脂结合会降低钙蛋白酶自溶所需的钙离子浓度[Ca2+],并且自溶会将无活性的酶原转化为活性蛋白酶。然而,最近的研究表明,钙蛋白酶与特定蛋白质而非磷脂结合,并且与细胞膜的结合不会影响自溶所需的[Ca2+]。钙蛋白酶活性似乎是通过钙离子与钙蛋白酶分子上特定位点的结合来调节的,与每个位点的结合都会引发针对该位点的特定反应(蛋白水解活性、钙蛋白酶抑制蛋白结合等)。调节还必须涉及一种尚未发现的机制,该机制会增加钙离子结合位点对钙离子的亲和力。