• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

在人类葡萄糖-6-磷酸酶-α的 298 位进行氨基酸替换会显著影响其在哺乳动物细胞中的稳定性。

Amnio acid substitution at position 298 of human glucose-6 phosphatase-α significantly impacts its stability in mammalian cells.

机构信息

Rare Diseases, Moderna, Inc., 200 Technology Square, Cambridge, MA, 02139, USA.

Platform, Moderna, Inc., 200 Technology Square, Cambridge, MA, 02139, USA.

出版信息

Amino Acids. 2023 May;55(5):695-708. doi: 10.1007/s00726-023-03263-8. Epub 2023 Mar 21.

DOI:10.1007/s00726-023-03263-8
PMID:36944899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10247848/
Abstract

Glucose-6-phosphatase-α (G6Pase-α) catalyzes the hydrolysis of glucose-6-phosphate to glucose and functions as a key regulator in maintaining blood glucose homeostasis. Deficiency in G6Pase-α causes glycogen storage disease 1a (GSD1a), an inherited disorder characterized by life-threatening hypoglycemia and other long-term complications. We have developed a potential mRNA-based therapy for GSD1a and demonstrated that a human G6Pase-α (hG6Pase-α) variant harboring a single serine (S) to cysteine (C) substitution at the amino acid site 298 (S298C) had > twofold increase in protein expression, resulting in improved in vivo efficacy. Here, we sought to investigate the mechanisms contributing to the increased expression of the S298C variant. Mutagenesis of hG6Pase-α identified distinct protein variants at the 298 amino acid position with substantial reduction in protein expression in cultured cells. Kinetic analysis of expression and subcellular localization in mammalian cells, combined with cell-free in vitro translation assays, revealed that altered protein expression stemmed from differences in cellular protein stability rather than biosynthetic rates. Site-specific mutagenesis studies targeting other cysteines of the hG6Pase-α S298C variant suggest the observed improvements in stability are not due to additional disulfide bond formation. The glycosylation at Asparagine (N)-96 is critical in maintaining enzymatic activity and mutations at position 298 mainly affected glycosylated forms of hG6Pase-α. Finally, proteasome inhibition by lactacystin improved expression levels of unstable hG6Pase-α variants. Taken together, these data uncover a critical role for a single amino acid substitution impacting the stability of G6Pase-α and provide insights into the molecular genetics of GSD1a and protein engineering for therapeutic development.

摘要

葡萄糖-6-磷酸酶-α(G6Pase-α)催化葡萄糖-6-磷酸水解为葡萄糖,是维持血糖稳态的关键调节剂。G6Pase-α 缺乏会导致糖原贮积病 1a 型(GSD1a),这是一种遗传性疾病,其特征是危及生命的低血糖和其他长期并发症。我们已经开发出一种针对 GSD1a 的潜在 mRNA 疗法,并证明在第 298 位氨基酸处单个丝氨酸(S)到半胱氨酸(C)取代的人 G6Pase-α(hG6Pase-α)变体的蛋白表达增加了两倍以上,从而提高了体内疗效。在这里,我们试图研究导致 S298C 变体表达增加的机制。hG6Pase-α 的突变鉴定出 298 位氨基酸位置的不同蛋白变体,在培养细胞中的蛋白表达显著降低。在哺乳动物细胞中进行表达和亚细胞定位的动力学分析,结合无细胞体外翻译测定,表明改变的蛋白表达源于细胞蛋白稳定性的差异,而不是生物合成率的差异。针对 hG6Pase-α S298C 变体其他半胱氨酸的定点突变研究表明,观察到的稳定性提高不是由于额外的二硫键形成。天冬酰胺(N)-96 的糖基化对于维持酶活性至关重要,而 298 位的突变主要影响 hG6Pase-α 的糖基化形式。最后,乳胞素抑制蛋白酶体可提高不稳定 hG6Pase-α 变体的表达水平。总之,这些数据揭示了单个氨基酸取代对 G6Pase-α 稳定性的关键作用,并为 GSD1a 的分子遗传学和治疗开发的蛋白质工程提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cf9/10247848/672c197ba0ce/726_2023_3263_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cf9/10247848/b37b752bebcf/726_2023_3263_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cf9/10247848/5d8d59ecadfc/726_2023_3263_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cf9/10247848/16775a81fe18/726_2023_3263_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cf9/10247848/609e8111037e/726_2023_3263_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cf9/10247848/672c197ba0ce/726_2023_3263_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cf9/10247848/b37b752bebcf/726_2023_3263_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cf9/10247848/5d8d59ecadfc/726_2023_3263_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cf9/10247848/16775a81fe18/726_2023_3263_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cf9/10247848/609e8111037e/726_2023_3263_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cf9/10247848/672c197ba0ce/726_2023_3263_Fig5_HTML.jpg

相似文献

1
Amnio acid substitution at position 298 of human glucose-6 phosphatase-α significantly impacts its stability in mammalian cells.在人类葡萄糖-6-磷酸酶-α的 298 位进行氨基酸替换会显著影响其在哺乳动物细胞中的稳定性。
Amino Acids. 2023 May;55(5):695-708. doi: 10.1007/s00726-023-03263-8. Epub 2023 Mar 21.
2
An evolutionary approach to optimizing glucose-6-phosphatase-α enzymatic activity for gene therapy of glycogen storage disease type Ia.优化葡萄糖-6-磷酸酶-α酶活性的进化方法用于糖原贮积病 Ia 型的基因治疗。
J Inherit Metab Dis. 2019 May;42(3):470-479. doi: 10.1002/jimd.12069. Epub 2019 Feb 22.
3
Structure-function analysis of human glucose-6-phosphatase, the enzyme deficient in glycogen storage disease type 1a.1a型糖原贮积病所缺乏的酶——人葡萄糖-6-磷酸酶的结构-功能分析
J Biol Chem. 1995 May 19;270(20):11882-6. doi: 10.1074/jbc.270.20.11882.
4
The molecular basis of glycogen storage disease type 1a: structure and function analysis of mutations in glucose-6-phosphatase.1a型糖原贮积病的分子基础:葡萄糖-6-磷酸酶突变的结构与功能分析
J Biol Chem. 2002 Feb 15;277(7):5047-53. doi: 10.1074/jbc.M110486200. Epub 2001 Dec 5.
5
Gene therapy using a novel G6PC-S298C variant enhances the long-term efficacy for treating glycogen storage disease type Ia.使用新型 G6PC-S298C 变异基因治疗增强了治疗糖原贮积病 Ia 型的长期疗效。
Biochem Biophys Res Commun. 2020 Jun 30;527(3):824-830. doi: 10.1016/j.bbrc.2020.04.124. Epub 2020 May 16.
6
Identification of mutations in the gene for glucose-6-phosphatase, the enzyme deficient in glycogen storage disease type 1a.葡萄糖-6-磷酸酶基因中突变的鉴定,该酶在1a型糖原贮积病中缺乏。
J Clin Invest. 1994 May;93(5):1994-9. doi: 10.1172/JCI117192.
7
Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type 1a.导致1a型糖原贮积病的葡萄糖-6-磷酸酶基因突变。
Science. 1993 Oct 22;262(5133):580-3. doi: 10.1126/science.8211187.
8
Transmembrane topology of glucose-6-phosphatase.葡萄糖-6-磷酸酶的跨膜拓扑结构
J Biol Chem. 1998 Mar 13;273(11):6144-8. doi: 10.1074/jbc.273.11.6144.
9
The molecular basis of type 1 glycogen storage diseases.1型糖原贮积病的分子基础。
Curr Mol Med. 2001 Mar;1(1):25-44. doi: 10.2174/1566524013364112.
10
A splice-switching oligonucleotide treatment ameliorates glycogen storage disease type 1a in mice with G6PC c.648G>T.一种剪接转换寡核苷酸疗法改善了 G6PC c.648G>T 突变的 1 型糖原贮积症小鼠的病情。
J Clin Invest. 2023 Dec 1;133(23):e163464. doi: 10.1172/JCI163464.

引用本文的文献

1
The induced-fit and catalytic mechanisms of human G6PC1.人葡萄糖-6-磷酸酶催化亚基1的诱导契合和催化机制
Cell Discov. 2025 Jul 15;11(1):62. doi: 10.1038/s41421-025-00814-z.
2
Chronic heat stress is capable of reducing the growth performance, causing damage to the liver structure, and altering the liver glucose metabolism and lipid metabolism in largemouth bass (Micropterus salmoides L.).长期热应激能够降低大口黑鲈(Micropterus salmoides L.)的生长性能,损害肝脏结构,并改变其肝脏葡萄糖代谢和脂质代谢。
Fish Physiol Biochem. 2025 Feb;51(1):24. doi: 10.1007/s10695-024-01416-4. Epub 2024 Dec 12.

本文引用的文献

1
Function of Protein S-Palmitoylation in Immunity and Immune-Related Diseases.蛋白 S-棕榈酰化在免疫和免疫相关疾病中的作用。
Front Immunol. 2021 Sep 7;12:661202. doi: 10.3389/fimmu.2021.661202. eCollection 2021.
2
mRNA therapy restores euglycemia and prevents liver tumors in murine model of glycogen storage disease.mRNA 疗法可恢复糖原贮积病小鼠模型的正常血糖水平并预防肝肿瘤。
Nat Commun. 2021 May 25;12(1):3090. doi: 10.1038/s41467-021-23318-2.
3
Protein S-Palmitoylation: advances and challenges in studying a therapeutically important lipid modification.
蛋白质 S-棕榈酰化:研究具有治疗重要性的脂质修饰的进展和挑战。
FEBS J. 2022 Feb;289(4):861-882. doi: 10.1111/febs.15781. Epub 2021 Mar 18.
4
Gene therapy using a novel G6PC-S298C variant enhances the long-term efficacy for treating glycogen storage disease type Ia.使用新型 G6PC-S298C 变异基因治疗增强了治疗糖原贮积病 Ia 型的长期疗效。
Biochem Biophys Res Commun. 2020 Jun 30;527(3):824-830. doi: 10.1016/j.bbrc.2020.04.124. Epub 2020 May 16.
5
Lipid nanoparticle-targeted mRNA therapy as a treatment for the inherited metabolic liver disorder arginase deficiency.靶向脂质纳米颗粒的 mRNA 疗法治疗遗传性代谢性肝脏疾病精氨酸酶缺乏症。
Proc Natl Acad Sci U S A. 2019 Oct 15;116(42):21150-21159. doi: 10.1073/pnas.1906182116. Epub 2019 Sep 9.
6
A New Era for Rare Genetic Diseases: Messenger RNA Therapy.罕见遗传病的新纪元:信使 RNA 疗法。
Hum Gene Ther. 2019 Oct;30(10):1180-1189. doi: 10.1089/hum.2019.090. Epub 2019 Jul 1.
7
mRNA Therapy Improves Metabolic and Behavioral Abnormalities in a Murine Model of Citrin Deficiency.mRNA 疗法改善 Citrin 缺乏症小鼠模型的代谢和行为异常。
Mol Ther. 2019 Jul 3;27(7):1242-1251. doi: 10.1016/j.ymthe.2019.04.017. Epub 2019 Apr 23.
8
Improved Efficacy in a Fabry Disease Model Using a Systemic mRNA Liver Depot System as Compared to Enzyme Replacement Therapy.与酶替代疗法相比,使用全身性 mRNA 肝脏储存系统可提高法布里病模型的疗效。
Mol Ther. 2019 Apr 10;27(4):878-889. doi: 10.1016/j.ymthe.2019.03.001. Epub 2019 Mar 6.
9
Systemic mRNA Therapy for the Treatment of Fabry Disease: Preclinical Studies in Wild-Type Mice, Fabry Mouse Model, and Wild-Type Non-human Primates.全身性 mRNA 疗法治疗法布雷病:野生型小鼠、法布雷病小鼠模型和野生型非人灵长类动物的临床前研究。
Am J Hum Genet. 2019 Apr 4;104(4):625-637. doi: 10.1016/j.ajhg.2019.02.003. Epub 2019 Mar 14.
10
Messenger RNA therapy for rare genetic metabolic diseases.信使 RNA 治疗罕见遗传性代谢疾病。
Gut. 2019 Jul;68(7):1323-1330. doi: 10.1136/gutjnl-2019-318269. Epub 2019 Feb 22.