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Biomol Concepts. 2011 Dec 1;2(6):469-480. doi: 10.1515/BMC.2011.041. Epub 2012 Jul 24.
2
Crystal structure of human senescence marker protein 30: insights linking structural, enzymatic, and physiological functions .人衰老标志物蛋白 30 的晶体结构:连接结构、酶学和生理学功能的见解。
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3
Comparative analysis of the metal-dependent structural and functional properties of mouse and human SMP30.比较分析小鼠和人 SMP30 的金属依赖性结构和功能特性。
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4
Involvement of senescence marker protein-30 in glucose metabolism disorder and non-alcoholic fatty liver disease.衰老标记蛋白-30与糖代谢紊乱及非酒精性脂肪性肝病的关系
Geriatr Gerontol Int. 2016 Mar;16 Suppl 1:4-16. doi: 10.1111/ggi.12722.
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Lactonases with organophosphatase activity: structural and evolutionary perspectives.具有有机磷酶活性的内酯酶:结构和进化视角。
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Deficiency of senescence marker protein 30 exacerbates angiotensin II-induced cardiac remodelling.衰老标志物蛋白 30 的缺乏会加剧血管紧张素 II 引起的心脏重构。
Cardiovasc Res. 2013 Aug 1;99(3):461-70. doi: 10.1093/cvr/cvt122. Epub 2013 May 30.
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Senescence marker protein 30 (SMP30) expression in eukaryotic cells: existence of multiple species and membrane localization.真核细胞中端粒酶相关蛋白 30(SMP30)的表达:多种物种的存在和膜定位。
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Release of SMP30 in Extracellular Vesicles under Conditions of Ascorbic Acid Deficiency Is Involved with Acute Phase Response in ODS Rat.在抗坏血酸缺乏条件下细胞外囊泡中 SMP30 的释放与 ODS 大鼠急性期反应有关。
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Senescence marker protein-30 is a unique enzyme that hydrolyzes diisopropyl phosphorofluoridate in the liver.衰老标记蛋白-30是一种独特的酶,可在肝脏中水解二异丙基氟磷酸酯。
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Senescence marker protein-30/superoxide dismutase 1 double knockout mice exhibit increased oxidative stress and hepatic steatosis.衰老标志物蛋白-30/超氧化物歧化酶 1 双重基因敲除小鼠表现出氧化应激增加和肝脂肪变性。
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World J Microbiol Biotechnol. 2023 Dec 20;40(2):45. doi: 10.1007/s11274-023-03843-6.
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Cancers (Basel). 2023 Nov 20;15(22):5489. doi: 10.3390/cancers15225489.
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RGN as a prognostic biomarker with immune infiltration and ceRNA in lung squamous cell carcinoma.RGN 作为肺鳞癌的预后生物标志物,与免疫浸润和 ceRNA 相关。
Sci Rep. 2023 May 9;13(1):7553. doi: 10.1038/s41598-023-32217-z.
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Senescence marker protein30 protects lens epithelial cells against oxidative damage by restoring mitochondrial function.衰老标志物蛋白 30 通过恢复线粒体功能保护晶状体上皮细胞免受氧化损伤。
Bioengineered. 2022 May;13(5):12955-12971. doi: 10.1080/21655979.2022.2079270.
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Effects of 6-Month Square Stepping Exercise Intervention on Physical and Cognitive Competence, Regucalcin, and Body Composition in Older People: Study Protocol for a Randomised Control Trial.6 个月方步走锻炼干预对老年人身体和认知能力、Regucalcin 及身体成分的影响:一项随机对照试验研究方案。
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New Evidence on Regucalcin, Body Composition, and Walking Ability Adaptations to Multicomponent Exercise Training in Functionally Limited and Frail Older Adults.关于多功能运动训练对功能受限和虚弱老年人的钙调节蛋白、身体成分和步行能力适应性的新证据。
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The Interplay of Vitamin D Deficiency and Cellular Senescence in The Pathogenesis of Obesity-Related Co-Morbidities.维生素 D 缺乏与细胞衰老在肥胖相关并发症发病机制中的相互作用。
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Senescence Marker Protein 30 (SMP30): A Novel Pan-Species Diagnostic Marker for the Histopathological Diagnosis of Breast Cancer in Humans and Animals.衰老标记蛋白30(SMP30):一种用于人类和动物乳腺癌组织病理学诊断的新型全物种诊断标志物。
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本文引用的文献

1
Regucalcin is broadly expressed in male reproductive tissues and is a new androgen-target gene in mammalian testis.钙调节蛋白广泛表达于雄性生殖组织,是哺乳动物睾丸中一个新的雄激素靶基因。
Reproduction. 2011 Sep;142(3):447-56. doi: 10.1530/REP-11-0085. Epub 2011 Jun 16.
2
Decreased senescence marker protein-30 could be a factor that contributes to the worsening of glucose tolerance in normal aging.衰老标志物蛋白-30 的减少可能是导致正常衰老过程中葡萄糖耐量恶化的一个因素。
Islets. 2010 Jul-Aug;2(4):258-60. doi: 10.4161/isl.2.4.12157.
3
Ascorbate synthesis pathway: dual role of ascorbate in bone homeostasis.抗坏血酸合成途径:抗坏血酸在骨稳态中的双重作用。
J Biol Chem. 2010 Jun 18;285(25):19510-20. doi: 10.1074/jbc.M110.110247. Epub 2010 Apr 21.
4
Regucalcin and metabolic disorders: osteoporosis and hyperlipidemia are induced in regucalcin transgenic rats.钙调节蛋白与代谢紊乱:钙调节蛋白转基因大鼠发生骨质疏松症和高脂血症。
Mol Cell Biochem. 2010 Aug;341(1-2):119-33. doi: 10.1007/s11010-010-0443-4. Epub 2010 Mar 28.
5
Crystal structure of human senescence marker protein 30: insights linking structural, enzymatic, and physiological functions .人衰老标志物蛋白 30 的晶体结构:连接结构、酶学和生理学功能的见解。
Biochemistry. 2010 Apr 27;49(16):3436-44. doi: 10.1021/bi9022297.
6
Structural characterization of the catalytic calcium-binding site in diisopropyl fluorophosphatase (DFPase)--comparison with related beta-propeller enzymes.二异丙基氟磷酸酶(DFPase)催化钙结合位点的结构特征 - 与相关β-发夹酶的比较。
Chem Biol Interact. 2010 Sep 6;187(1-3):373-9. doi: 10.1016/j.cbi.2010.02.043. Epub 2010 Mar 3.
7
Complete lack of vitamin C intake generates pulmonary emphysema in senescence marker protein-30 knockout mice.完全缺乏维生素 C 的摄入会导致衰老标志物蛋白-30 敲除小鼠发生肺气肿。
Am J Physiol Lung Cell Mol Physiol. 2010 Jun;298(6):L784-92. doi: 10.1152/ajplung.00256.2009. Epub 2010 Feb 19.
8
Vitamin C deficiency attenuates liver fibrosis by way of up-regulated peroxisome proliferator-activated receptor-gamma expression in senescence marker protein 30 knockout mice.维生素 C 缺乏通过上调衰老标记蛋白 30 敲除小鼠中过氧化物酶体增殖物激活受体-γ的表达来减轻肝纤维化。
Hepatology. 2010 May;51(5):1766-77. doi: 10.1002/hep.23499.
9
Lactonases with organophosphatase activity: structural and evolutionary perspectives.具有有机磷酶活性的内酯酶:结构和进化视角。
Chem Biol Interact. 2010 Sep 6;187(1-3):370-2. doi: 10.1016/j.cbi.2010.01.039. Epub 2010 Feb 1.
10
Ascorbic acid depletion enhances expression of the sodium-dependent vitamin C transporters, SVCT1 and SVCT2, and uptake of ascorbic acid in livers of SMP30/GNL knockout mice.抗坏血酸耗竭增强了 SMP30/GNL 敲除小鼠肝脏中钠离子依赖型维生素 C 转运体 SVCT1 和 SVCT2 的表达和抗坏血酸摄取。
Arch Biochem Biophys. 2010 Apr 1;496(1):38-44. doi: 10.1016/j.abb.2010.01.012. Epub 2010 Feb 1.

衰老标记蛋白30:对其未知生理功能的功能与结构见解

Senescence Marker Protein 30: Functional and Structural Insights to its Unknown Physiological Function.

作者信息

Scott Stephanie H, Bahnson Brian J

机构信息

Department of Chemistry & Biochemistry, University of Delaware, Newark, DE 19716, USA.

出版信息

Biomol Concepts. 2011 Dec 1;2(6):469-480. doi: 10.1515/BMC.2011.041. Epub 2012 Jul 24.

DOI:10.1515/BMC.2011.041
PMID:22844387
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3405729/
Abstract

Senescence marker protein 30 (SMP30) is a multifunctional protein involved in cellular Ca(2+) homeostasis and the biosynthesis of ascorbate in non-primate mammals. The primary structure of the protein is highly conserved among vertebrates, suggesting the existence of a significant physiological function common to all mammals, including primates. Enzymatic activities of SMP30 include aldonolactone and organophosphate hydrolysis. Protective effects against apoptosis and oxidative stress have been reported. X-ray crystallography revealed that SMP30 is a six-bladed β-propeller with structural similarity to paraoxonase 1, another protein with lactonase and organophosphate hydrolase activities. SMP30 has recently been tied to several physiological conditions including osteoporosis, liver fibrosis, diabetes, and cancer. This review aims to describe the recent advances made toward understanding the connection between molecular structure, enzymatic activity and physiological function of this highly conserved, multifaceted protein.

摘要

衰老标记蛋白30(SMP30)是一种多功能蛋白,参与非灵长类哺乳动物细胞内的钙稳态和抗坏血酸生物合成。该蛋白的一级结构在脊椎动物中高度保守,这表明包括灵长类动物在内的所有哺乳动物都存在重要的共同生理功能。SMP30的酶活性包括醛糖内酯和有机磷酸酯水解。据报道,它具有抗细胞凋亡和氧化应激的保护作用。X射线晶体学研究表明,SMP30是一种六叶β-螺旋桨蛋白,其结构与对氧磷酶1相似,后者也是一种具有内酯酶和有机磷酸酯水解酶活性的蛋白。最近,SMP30与包括骨质疏松症、肝纤维化、糖尿病和癌症在内的多种生理状况相关。本综述旨在描述在理解这种高度保守、多功能蛋白的分子结构、酶活性和生理功能之间的联系方面取得的最新进展。