The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA; email:
Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Annu Rev Biochem. 2024 Aug;93(1):317-338. doi: 10.1146/annurev-biochem-030222-121901.
Discovered in 1993, inositol pyrophosphates are evolutionarily conserved signaling metabolites whose versatile modes of action are being increasingly appreciated. These include their emerging roles as energy regulators, phosphodonors, steric/allosteric regulators, and G protein-coupled receptor messengers. Through studying enzymes that metabolize inositol pyrophosphates, progress has also been made in elucidating the various cellular and physiological functions of these pyrophosphate-containing, energetic molecules. The two main forms of inositol pyrophosphates, 5-IP and IP, synthesized respectively by inositol-hexakisphosphate kinases (IP6Ks) and diphosphoinositol pentakisphosphate kinases (PPIP5Ks), regulate phosphate homeostasis, ATP synthesis, and several other metabolic processes ranging from insulin secretion to cellular energy utilization. Here, we review the current understanding of the catalytic and regulatory mechanisms of IP6Ks and PPIP5Ks, as well as their counteracting phosphatases. We also highlight the genetic and cellular evidence implicating inositol pyrophosphates as essential mediators of mammalian metabolic homeostasis.
肌醇六磷酸酶和双磷酸肌醇五磷酸酶分别合成的两种主要的肌醇焦磷酸形式 5-IP 和 IP 调节着磷酸盐稳态、ATP 合成以及从胰岛素分泌到细胞能量利用等多种代谢过程。在此,我们综述了目前对 IP6K 和 PPIP5K 的催化和调控机制及其拮抗磷酸酶的理解,同时还强调了遗传和细胞证据表明肌醇焦磷酸盐是哺乳动物代谢稳态的必需介质。
解析:
文中“inositol-hexakisphosphate kinases (IP6Ks)”、“diphosphoinositol pentakisphosphate kinases (PPIP5Ks)”可直译为“肌醇六磷酸酶”和“双磷酸肌醇五磷酸酶”。
“5-IP”和“IP”可直译为“5-IP”和“IP”。
“homeostasis”可直译为“稳态”。
“metabolic homeostasis”可直译为“代谢稳态”。