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乙酰-4'-磷酸泛酰巯基乙胺在血清中稳定,并可预防泛酸激酶缺乏引起的表型。

Acetyl-4'-phosphopantetheine is stable in serum and prevents phenotypes induced by pantothenate kinase deficiency.

机构信息

Division of Molecular Neurogenetics, IRCCS Foundation Neurological Institute "C.Besta" Via Temolo 4, 20126, Milano, Italy.

Department of Cell Biology, University Medical Center Groningen, University of Groningen, Ant. Deusinglaan 1, 9713 AV, Groningen, The Netherlands.

出版信息

Sci Rep. 2017 Sep 12;7(1):11260. doi: 10.1038/s41598-017-11564-8.

Abstract

Coenzyme A is an essential metabolite known for its central role in over one hundred cellular metabolic reactions. In cells, Coenzyme A is synthesized de novo in five enzymatic steps with vitamin B5 as the starting metabolite, phosphorylated by pantothenate kinase. Mutations in the pantothenate kinase 2 gene cause a severe form of neurodegeneration for which no treatment is available. One therapeutic strategy is to generate Coenzyme A precursors downstream of the defective step in the pathway. Here we describe the synthesis, characteristics and in vivo rescue potential of the acetyl-Coenzyme A precursor S-acetyl-4'-phosphopantetheine as a possible treatment for neurodegeneration associated with pantothenate kinase deficiency.

摘要

辅酶 A 是一种必需的代谢物,已知其在一百多种细胞代谢反应中起着核心作用。在细胞中,辅酶 A 通过维生素 B5 作为起始代谢物经五个酶促步骤从头合成,然后被泛酸激酶磷酸化。泛酸激酶 2 基因的突变会导致一种严重的神经退行性疾病,目前尚无治疗方法。一种治疗策略是在该途径的缺陷步骤下游生成辅酶 A 前体。本文描述了作为泛酸激酶缺乏症相关神经退行性疾病潜在治疗方法的乙酰辅酶 A 前体 S-乙酰-4′-磷酸泛酰巯基乙胺的合成、特性和体内挽救潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14b0/5595861/28a50bf45215/41598_2017_11564_Fig1_HTML.jpg

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