Molecular Characterization and Cytotoxic Activity of McTI, a Novel Cystine-Knot Inhibitor from Momordica charantia.

Yamna Khurshid, M. Saeed, Jerika T. Lam, S. Simjee, Z. Haq, Aftab Ahmed, Allis Chien, Roy Martin
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引用次数: 1

Abstract

Medicinal plants are rich source of pharmaceutically active peptides and proteins. Momordica charantia, a traditional medicinal plant commonly known as bitter melon, is a member of a family Cucurbitaceae and has been explored for various human diseases such as diabetes, peptic ulcer, malaria, infectious diseases, and cancer. Yet, to date only a handful of studies are available related to the therapeutic potential of Momordica charantia seed proteins. In present study, a novel trypsin inhibitor McTI was purified by 2D-LC technique from ammonium sulphate precipitated crude seed proteins of Momordica charantia. The crude seed proteins and gel filtration fractions were explored for their cytotoxic response against MDA-MB-231 cells. Later, for deeper understanding, complete amino acid sequence of McTI was established by Edman protein sequencing and 3D structure was predicted by comparative homology modeling using template trypsin inhibitor 3 from spiny bitter cucumber. In silico molecular docking and dynamic simulation experiments were also performed to study the interaction of McTI with bovine trypsin. The results revealed that McTI is a 30 amino acids peptide having a molecular mass of 3388.4 Da and showed sequence similarity with previously reported cystine knot trypsin inhibitors from plant. McTI is a disulfide rich peptide having 6 cysteine residues that can form 3 disulfide bonds (Cys3-Cys20, Cys10-Cys22 and Cys16-Cys28). Six hydrogen bond interactions of McTI with bovine trypsin were observed in molecular docking whereas, additional hydrogen bond interactions were noticed in molecular dynamic simulation studies. In cytotoxicity analysis against MDA-MB-231 cells, crude seed proteins and F12 exhibited a significant dose dependent response with an IC 50 values of 82.10 ± 6.46 µg/ml and 81.13 ± 4.26, respectively. These findings suggest Momordica charantia proteins as a possible anticancer agent. Furthermore, McTI is a valuable addition in the squash inhibitor family.
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苦瓜半胱氨酸结抑制剂McTI的分子特性及细胞毒活性研究。
药用植物是药用活性肽和蛋白质的丰富来源。苦瓜(Momordica charantia)是一种传统药用植物,俗称苦瓜,是葫芦科的一员,已被探索用于治疗各种人类疾病,如糖尿病、消化性溃疡、疟疾、传染病和癌症。然而,到目前为止,只有少数研究与苦瓜种子蛋白质的治疗潜力有关。本研究以苦瓜(Momordica charantia)种子粗蛋白为原料,采用2D-LC技术纯化了一种新型胰蛋白酶抑制剂McTI。研究了粗种子蛋白和凝胶过滤组分对MDA-MB-231细胞的细胞毒反应。随后,为了更深入的了解McTI,我们利用Edman蛋白测序建立了McTI的完整氨基酸序列,并利用苦刺黄瓜胰蛋白酶抑制剂3模板,通过比较同源性建模预测了McTI的三维结构。通过分子对接和动态模拟实验研究了McTI与牛胰蛋白酶的相互作用。结果表明,McTI是一个由30个氨基酸组成的肽,分子量为3388.4 Da,与先前报道的植物胱氨酸结胰蛋白酶抑制剂序列相似。McTI是一种富含二硫的肽,具有6个半胱氨酸残基,可以形成3个二硫键(Cys3-Cys20、Cys10-Cys22和Cys16-Cys28)。在分子对接中观察到McTI与牛胰蛋白酶的6个氢键相互作用,在分子动力学模拟中观察到额外的氢键相互作用。在对MDA-MB-231细胞的细胞毒性分析中,粗种子蛋白和F12表现出显著的剂量依赖性,ic50值分别为82.10 ±6.46 µg/ml和81.13 ±4.26。这些发现表明,苦瓜蛋白可能是一种抗癌剂。此外,McTI是壁球抑制剂家族中一个有价值的补充。
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