Comis A, Easterbrook-Smith S B
FEBS Lett. 1985 Jun 3;185(1):105-8. doi: 10.1016/0014-5793(85)80749-3.
Mitochondrial preparations, obtained from human tonsils and from rat spleen, liver, heart, and kidney tissues, bound [125I]C1q with affinities of 10(7)-10(8)M-1. The binding of C1q was not affected by treatment of the mitochondrial preparations with pronase, trypsin, or phospholipase D, but it was lowered 5-6-fold following treatment of the mitochondria with DNase and RNase. Binding of C1q to mitochondrial preparations was also greatly diminished by limited chemical modification of C1q with cyclohexane-1,2-dione. It is suggested that the reported binding of C1q to mitochondria may have arisen from the protein binding to DNA and/or RNA contaminating the mitochondrial preparations.
从人扁桃体以及大鼠脾脏、肝脏、心脏和肾脏组织中获得的线粒体制剂,以10⁷ - 10⁸M⁻¹的亲和力结合[¹²⁵I]C1q。用链霉蛋白酶、胰蛋白酶或磷脂酶D处理线粒体制剂后,C1q的结合不受影响,但用DNA酶和RNA酶处理线粒体后,其结合降低了5 - 6倍。用环己烷-1,2-二酮对C1q进行有限的化学修饰,也大大降低了C1q与线粒体制剂的结合。有人提出,所报道的C1q与线粒体的结合可能是由于蛋白质与污染线粒体制剂的DNA和/或RNA结合所致。