Isolation and characterization of phosphoglycerate kinase and creatine kinase from bighead carp (Aristichthys nobilis): Potential sources for antitumor agents.

IF 1.9 Q3 PHARMACOLOGY & PHARMACY
Drug Discoveries and Therapeutics Pub Date : 2025-03-06 Epub Date: 2025-02-26 DOI:10.5582/ddt.2025.01003
Yue Gao, Wanying Liu, Qing Yan, Chunlei Li, Mengke Gu, Sixue Bi, Weiming Zheng, Jianhua Zhu, Liyan Song, Rongmin Yu
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Abstract

Bighead carp (Aristichthys nobilis) has garnered significant attention due to its potential health benefits, yet its bioactive protein components remain largely unexplored. In this study, two proteins S3 and Z1 were isolated from Aristichthys nobilis using ammonium sulfate precipitation and serial column chromatography guided by their in vitro antitumor activity. Both proteins were found to be homogeneous in sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) with a purity exceeding 95% as confirmed by reverse-phase high performance liquid chromatography (RP-HPLC). Electrospray ionization tandem mass spectrometry (ESI-MS/MS) analysis revealed their precise molecular weights to be 44.335 kDa for S3 and 43.028 kDa for Z1. Their amino acid sequences were elucidated through tandem mass spectroscopy and transcriptome unigene analysis, identifying S3 as phosphoglycerate kinase and Z1 as creatine kinase. Furthermore, secondary structure was measured by circular dichroism and three-dimensional structure was predicted by modeling software. The antitumor potential of S3 was evaluated by an in vitro assay, yielding an IC50 value of 26.3 ± 2.9 μM against the HT-29 cell line. Z1 demonstrated antiproliferative activity in vitro with IC50 values of 21.8 ± 1.4, 22.3 ± 2.1, and 22.3 ± 2.5 μM against HT-29, HeLa, and HepG2 cell lines, respectively. Notably, Z1 was found to enhance glucose metabolism and significantly increase the production of lactic acid and CO2 in tumor cells. These findings suggest that bighead carp (A. nobilis) could serve as a promising source for both antitumor agents and functional food ingredients.

鳙鱼磷酸甘油酸激酶和肌酸激酶的分离与鉴定:抗肿瘤药物的潜在来源。
鳙鱼(Aristichthys nobilis)因其潜在的健康益处而引起了极大的关注,但其生物活性蛋白成分在很大程度上仍未被探索。本研究利用硫酸铵沉淀法和串联柱层析法,从野马鱼中分离得到两个蛋白S3和Z1,并对其体外抗肿瘤活性进行了研究。经十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)证实,两种蛋白均为均相,反相高效液相色谱(RP-HPLC)证实,纯度均超过95%。电喷雾电离串联质谱(ESI-MS/MS)分析表明,S3和Z1的精确分子量分别为44.335 kDa和43.028 kDa。通过串联质谱和转录组单基因分析鉴定了它们的氨基酸序列,S3为磷酸甘油激酶,Z1为肌酸激酶。利用圆二色性测量了二次结构,并用建模软件预测了三维结构。体外实验表明,S3对HT-29细胞株的IC50值为26.3±2.9 μM。Z1对HT-29、HeLa和HepG2细胞株的IC50分别为21.8±1.4、22.3±2.1和22.3±2.5 μM。值得注意的是,Z1被发现可以促进肿瘤细胞的葡萄糖代谢,并显著增加乳酸和CO2的产生。研究结果表明,鳙鱼可作为抗肿瘤药物和功能性食品原料的重要来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug Discoveries and Therapeutics
Drug Discoveries and Therapeutics PHARMACOLOGY & PHARMACY-
CiteScore
3.20
自引率
3.20%
发文量
51
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