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FAMIN是一种实现嘌呤核苷酸循环的多功能酶
作者:小柯机器人 发布时间:2020/2/6 9:24:17

近日,英国剑桥大学Arthur Kaser小组发现FAMIN是一个实现嘌呤核苷酸循环的多功能嘌呤酶。2020年1月23日出版的《细胞》发表了这项成果。

据研究人员介绍,FAMIN突变会在儿童早期引起关节炎和炎症性肠病,并且一种常见的遗传变异会增加克罗恩病和麻风病的风险。
 
研究人员开发了一种无偏倚液相色谱-质谱筛查该孤儿蛋白的酶活性。研究人员发现,FAMIN磷解性剪切腺苷成腺嘌呤和1-磷酸核糖。这种活性以往不认为存在于真核代谢中。FAMIN及其原核直系同源基因还具有腺苷脱氨酶、嘌呤核苷磷酸化酶和S-甲基-5'-硫代腺苷磷酸化酶活性,因此兼具核心嘌呤代谢的同名酶活性。FAMIN使得巨噬细胞中的腺苷和肌苷单磷酸与腺苷琥珀酸酯之间存在了一个嘌呤核苷酸循环(PNC),从而能够消耗天冬氨酸并以涉及脂肪酸氧化和ATP柠檬酸裂解酶活性的方式释放富马酸酯。这一巨噬细胞的PNC通过平衡线粒体电子转移,使线粒体活性与糖酵解同步化,从而支持糖酵解活性并促进氧化磷酸化以及线粒体H+和磷酸盐的循环利用。
 
附:英文原文

Title: FAMIN Is a Multifunctional Purine Enzyme Enabling the Purine Nucleotide Cycle

Author: M. Zaeem Cader, Rodrigo Pereira de Almeida Rodrigues, James A. West, Gavin W. Sewell, Muhammad N. Md-Ibrahim, Stephanie Reikine, Giuseppe Sirago, Lukas W. Unger, Ana Belén Inglesias-Romero, Katharina Ramshorn, Lea-Maxie Haag, Svetlana Saveljeva, Jana-Fabienne Ebel, Philip Rosenstiel, Nicole C. Kaneider, James C. Lee, Trevor D. Lawley, Allan Bradley, Gordon Dougan, Yorgo Modis, Julian L. Griffin, Arthur Kaser

Issue&Volume: 2020/01/23

Abstract: Mutations in FAMIN cause arthritis and inflammatory bowel disease in early childhood, and a common genetic variant increases the risk for Crohn's disease and leprosy. We developed an unbiased liquid chromatography-mass spectrometry screen for enzymatic activity of this orphan protein. We report that FAMIN phosphorolytically cleaves adenosine into adenine and ribose-1-phosphate. Such activity was considered absent from eukaryotic metabolism. FAMIN and its prokaryotic orthologs additionally have adenosine deaminase, purine nucleoside phosphorylase, and S-methyl-5′-thioadenosine phosphorylase activity, hence, combine activities of the namesake enzymes of central purine metabolism. FAMIN enables in macrophages a purine nucleotide cycle (PNC) between adenosine and inosine monophosphate and adenylosuccinate, which consumes aspartate and releases fumarate in a manner involving fatty acid oxidation and ATP-citrate lyase activity. This macrophage PNC synchronizes mitochondrial activity with glycolysis by balancing electron transfer to mitochondria, thereby supporting glycolytic activity and promoting oxidative phosphorylation and mitochondrial H+ and phosphate recycling.

DOI: 10.1016/j.cell.2019.12.017

Source: https://www.cell.com/cell/fulltext/S0092-8674(19)31379-0

期刊信息
Cell:《细胞》,创刊于1974年。隶属于细胞出版社,最新IF:36.216
官方网址:https://www.cell.com/