Cytotoxicity and antioxidant activity of Kamolonol acetate from Ferula pseudalliacea, and studying its interactions with calf thymus DNA (ct-DNA) and human serum albumin (HSA) by spectroscopic and molecular docking techniques

Hanie Mahaki, Hamid Tanzadehpanah, Osama Abou-Zied, Neda Hosseinpour Moghadam, Asrin Bahmani, Sadegh Salehzadeh, Dara Dastan*, Massoud Saidijam

*المؤلف المقابل لهذا العمل

نتاج البحث: المساهمة في مجلةمراجعة النظراء

31 اقتباسات (Scopus)

ملخص

In this study, kamolonol acetate (KamA) was extracted from Ferula pseudalliacea and its cytotoxicity, antioxidant activities, calf thymus DNA (DNA) and human serum albumin (HSA) binding properties were evaluated by several methods. The cytotoxicity of the KamA against two colorectal cancer cell lines (HCT116 and CT26) and two normal cell lines (mesenchymal stem cells and Vero cells) was determined with IC50 values of 27, 17, 47, and 72 μM, respectively. KamA also showed a potent antioxidant activity on the DPPH radical scavenging (EC50 = 65.29 μM). The results obtained from DNA binding evaluations using DNA competitive displacement and viscosity measurements showed that KamA can bind to DNA via an intercalation mode. Binding activity of HSA exhibited that KamA can strongly quench the intrinsic fluorescence of HSA through a static quenching mode (distance = 2.22 nm). We also found that the KamA binding site on HSA is located in sub-domain IIA. Furthermore, the zeta-potential measurements showed that both electrostatic and hydrophobic interactions play a critical role in the formation of [DNA-KamA] and [HSA-KamA] complexes. Finally, molecular docking supported the experimental results in binding sites and binding forces. As a conclusion, we suggested that KamA can be introduced as a bioactive compound.

اللغة الأصليةEnglish
دوريةProcess Biochemistry
المعرِّفات الرقمية للأشياء
حالة النشرAccepted/In press - يناير 1 2018

ASJC Scopus subject areas

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بصمة

أدرس بدقة موضوعات البحث “Cytotoxicity and antioxidant activity of Kamolonol acetate from Ferula pseudalliacea, and studying its interactions with calf thymus DNA (ct-DNA) and human serum albumin (HSA) by spectroscopic and molecular docking techniques'. فهما يشكلان معًا بصمة فريدة.

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