Kim H, Jacobson E L, Jacobson M K
Department of Biochemistry and Molecular Biology, University of North Texas Health Science Center at Fort Worth 76107.
Science. 1993 Sep 3;261(5126):1330-3. doi: 10.1126/science.8395705.
Cyclic adenosine diphosphoribose (cADPR), a recently discovered metabolite of nicotinamide adenine dinucleotide (NAD), is a potent calcium-releasing agent postulated to be a new second messenger. An enzyme that catalyzes the synthesis of cADPR from NAD and the hydrolysis of cADPR to ADP-ribose (ADPR) was purified to homogeneity from canine spleen microsomes. The net conversion of NAD to ADPR categorizes this enzyme as an NAD glycohydrolase. NAD glycohydrolases are ubiquitous membrane-bound enzymes that have been known for many years but whose function has not been identified. The results presented here suggest that these enzymes may function in the regulation of calcium homeostasis by the ability to synthesize and degrade cADPR.
环磷酸腺苷二磷酸核糖(cADPR)是最近发现的烟酰胺腺嘌呤二核苷酸(NAD)的代谢产物,是一种强效的钙释放剂,被认为是一种新的第二信使。一种催化从NAD合成cADPR以及将cADPR水解为ADP-核糖(ADPR)的酶,已从犬脾微粒体中纯化至同质。NAD向ADPR的净转化将这种酶归类为NAD糖水解酶。NAD糖水解酶是普遍存在的膜结合酶,多年来已为人所知,但其功能尚未确定。此处给出的结果表明,这些酶可能通过合成和降解cADPR的能力在钙稳态调节中发挥作用。