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Coenzyme A Sale

(Synonyms: 辅酶 A) 目录号 : GC43293

Coenzyme A是一种活细胞中不可或缺的辅因子,由泛酸(维生素B5)、三磷酸腺苷(ATP)和半胱氨酸合成。

Coenzyme A Chemical Structure

Cas No.:85-61-0

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10mM (in 1mL DMSO)
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1mg
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10mg
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25mg
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Sample solution is provided at 25 µL, 10mM.

Description

Coenzyme A is an indispensable cofactor in living cells, synthesized from pantothenic acid (vitamin B5), adenosine triphosphate (ATP), and cysteine [1]. As an acyl carrier and carbonyl activating group, Coenzyme A plays a crucial role in the oxidation of pyruvate in the citric acid cycle and the metabolism of carboxylic acids (including short-chain and long-chain fatty acids) [2]. Abnormalities in the biosynthesis and homeostasis of Coenzyme A and its derivatives are associated with various human diseases, including cancer, diabetes, and neurodegeneration [3].

In vitro, supplementing Coenzyme A (25μM; 30 days) in the culture medium can significantly restore the function and mitochondrial respiratory activity of neuronal cells from patients with Pantothenate kinase-associated neurodegenerative disease (PKAN), while inhibiting neuronal death and ROS formation [4]. Coenzyme A (1mM; 30min) can completely inhibit the activity of peroxiredoxin 5 (Prdx5), and this inhibitory state can be relieved by dithiothreitol (DTT) reduction [5].

References:
[1] Michal G, Bergmeyer H U. Coenzyme A[M]//Methods of enzymatic analysis. Academic Press, 1974: 1967-1987.
[2] Leonardi R, Zhang YM, Rock CO, Jackowski S. Coenzyme A: back in action. Prog Lipid Res. 2005;44(2-3):125-153.
[3] Tsuchiya Y, Peak-Chew SY, Newell C, et al. Protein CoAlation: a redox-regulated protein modification by coenzyme A in mammalian cells. Biochem J. 2017;474(14):2489-2508. Published 2017 Jul 11.
[4] Orellana DI, Santambrogio P, Rubio A, et al. Coenzyme A corrects pathological defects in human neurons of PANK2-associated neurodegeneration. EMBO Mol Med. 2016;8(10):1197-1211.
[5] Baković J, Yu B Y K, Silva D, et al. A key metabolic integrator, coenzyme A, modulates the activity of peroxiredoxin 5 via covalent modification[J]. Molecular and cellular biochemistry, 2019, 461(1): 91-102.

Coenzyme A是一种活细胞中不可或缺的辅因子,由泛酸(维生素B5)、三磷酸腺苷(ATP)和半胱氨酸合成 [1]。Coenzyme A作为酰基载体和羰基活化基团,在柠檬酸循环中丙酮酸的氧化以及羧酸(包括短链和长链脂肪酸)的代谢过程中起重要作用 [2]。Coenzyme A及其衍生物的生物合成和稳态异常与多种人类疾病有关,包括癌症、糖尿病和神经退行性变 [3]

在体外,在培养基中补充Coenzyme A(25μM; 30 days)能够显著恢复来自Pantothenate激酶相关神经退行性疾病(PKAN)患者的神经元细胞的功能和线粒体呼吸活性,同时抑制神经元死亡和ROS形成 [4]。Coenzyme A(1mM; 30min)能够完全抑制过氧化物酶5(Prdx5)的活性,这种抑制状态可通过二硫苏糖醇(DTT)还原来解除 [5]

实验参考方法

Cell experiment [1]:

Cell lines

Human neuronal precursors cells and neurons (NPCs)

Preparation Method

NPCs from Pantothenate kinase‐associated neurodegeneration (PKAN) patients were seeded on Matrigel‐coated wells and differentiated in medium containing Neurobasal, BDNF (10ng/ml), NT‐3 (10ng/ml), B27, P/S, and doxycycline (2μg/ml). A final concentration of 25μM Coenzyme A was added to treat the cells. Coenzyme A was resuspended in a Neurobasal medium and stored at −20°C. Fresh medium containing Coenzyme A (25μM) was added every 2 days to the cells undergoing treatment. Measure the mitochondrial membrane potential, ROS, the morphology of dendritic branches, and determine the activity of aconitase in neurons.

Reaction Conditions

25μM; 30 days

Applications

Supplementation of Coenzyme A in the culture medium can significantly restore the function of neurons related to PKAN disease and the mitochondrial respiratory activity, preventing neuronal death and ROS formation.

References:
[1] Orellana DI, Santambrogio P, Rubio A, et al. Coenzyme A corrects pathological defects in human neurons of PANK2-associated neurodegeneration. EMBO Mol Med. 2016;8(10):1197-1211.

化学性质

Cas No. 85-61-0 SDF
别名 辅酶 A
Canonical SMILES O[C@H]1[C@H](N2C=NC3=C2N=CN=C3N)O[C@H](COP(OP(OCC(C)(C)[C@@H](O)C(NCCC(NCCS)=O)=O)(O)=O)(O)=O)[C@H]1OP(O)(O)=O
分子式 C21H36N7O16P3S 分子量 767.5
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1 mM 1.3029 mL 6.5147 mL 13.0293 mL
5 mM 260.6 μL 1.3029 mL 2.6059 mL
10 mM 130.3 μL 651.5 μL 1.3029 mL
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