期刊
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
卷 135, 期 -, 页码 106-115出版社
ELSEVIER
DOI: 10.1016/j.jpba.2016.12.001
关键词
Human serum alpha-1 acid glycoprotein; Human serum albumin; Fluorescence quenching; Circular dichroism; Molecular docking; Anticancer; Clofarabine
资金
- University Grants Commission, New Delhi
- Department of biotechnology, Government of India
- Deanship of Scientific Research at king Saud University [RG-1435-019]
The binding interaction between clofarabine, an important anticancer drug and two important carrier proteins found abundantly in human plasma, Human Serum Albumin (HSA) and alpha-1 acid glycoprotein (AAG) was investigated by spectroscopic and molecular modeling methods. The results obtained from fluorescence quenching experiments demonstrated that the fluorescence intensity of HSA and AAG is quenched by clofarabine and the static mode of fluorescence quenching is operative. UV-vis spectroscopy deciphered the formation of ground state complex between anticancer drug and the two studied proteins. Clofarabine was found to bind at 298 K with both AAG and HSA with the binding constant of 8.128 x 10(3) and 4.120 x 10(3) for AAG and HSA, respectively. There is stronger interaction of clofarabine with MG as compared to HSA. The Gibbs free energy change was found to be negative for the interaction of clofarabine with AAG and HSA indicating that the binding process is spontaneous. Binding of clofarabine with HSA and AAG induced ordered structures in both proteins and lead to molecular compaction. Clofarabine binds to HSA near to drug site II. Hydrogen bonding and hydrophobic interactions were the main bonding forces between HSA-clofarabine and AAG-clofarabine as revealed by docking results. This study suggests the importance of binding of anticancer drug to AAG spatially in the diseases like cancers where the plasma concentration of AAG increases many folds. Design of drug dosage can be adjusted accordingly to achieve optimal treatment outcome. (C) 2016 Elsevier B.V. All rights reserved.
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