An ester-functionalized cationic gemini surfactant mediated structural transitions of porcine serum albumin (PSA) via binding interaction

被引:6
作者
Akram, Mohd. [1 ]
Ansari, Farah [1 ]
Bhat, Imtiyaz Ahmad [1 ]
Chaturvedi, Sumit Kumar [2 ]
Khan, Rizwan Hasan [2 ]
Kabir-ud-Din [1 ,3 ]
机构
[1] Aligarh Muslim Univ, Dept Chem, Aligarh 202002, Uttar Pradesh, India
[2] Aligarh Muslim Univ, Interdisciplinary Biotechnol Unit, Aligarh 202002, Uttar Pradesh, India
[3] Arba Minch Univ, Dept Chem, Arba Minch, Ethiopia
关键词
Porcine serum albumin (PSA); 16-E2-16; Structural transitions; SODIUM DODECYL-SULFATE; ETHANE-1,2-DIYL BIS(N,N-DIMETHYL-N-HEXADECYLAMMONIUMACETOXY) DICHLORIDE; MOLECULAR DOCKING; IMIDAZOLIUM SURFACTANTS; IONIC SURFACTANTS; LIGHT-SCATTERING; FLUORESCENCE; PROTEIN; PROBE; SPECTROSCOPY;
D O I
10.1016/j.colsurfa.2016.12.028
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Keeping in mind the contemporary environmental concern raised over the disposal of surfactants into water bodies, we synthesized biodegradable cationic gemini surfactant ethane-1,2-diyl bis(N,N-dimethyl-N-hexadecylammoniumacetoxy) dichloride (16-E2-16), which bears easily cleavable ester functionalities (betaine type arrangement) in its spacer. This research article encompasses an in vitro analysis of the interaction between the synthesized gemini surfactant and a serum transport protein, porcine serum albumin (PSA) under physiological mimetic conditions. A multi-technique approach was exploited to explore the structural alterations induced in PSA at different concentrations of 16-E2-16. Fluorescence measurements unraveled a substantial interaction between PSA and 16-E2-16 (K-b similar to 10(4) M-1). Synchronous and three-dimensional fluorescence spectra further validated the binding of 16-E2-16 with PSA. Pyrene emission fluorescence depicted an increased hydrophilicity experienced by the probe molecules on account of their expulsion into the solvent due to a comparatively stronger binding of the gemini surfactant with PSA. The UV-vis studies established the ground state complexation of the gemini with PSA. Interestingly, far-UV CD results demonstrated the stabilization of secondary structure of PSA at concentrations below and above the CMC of 16-E2-16. Near-UV CD spectra revealed negligible changes in the tertiary structure of PSA. Additonally, CV scans depicted electrochemically inactive 16-E2-16-PSA complex formation and thus reinforced the findings of spectroscopic investigations. Overall, it is inferred that 16-E2-16 binds efficiently with PSA affecting both its microenvironment and conformation. Owing to these favorable interactions, 16-E2-16 may find its application as a prospective excipient in drug, skincare and immunoassay reagent formulations, in which serum albumins are frequently used. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:245 / 253
页数:9
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