期刊
JOURNAL OF HAZARDOUS MATERIALS
卷 175, 期 1-3, 页码 985-991出版社
ELSEVIER
DOI: 10.1016/j.jhazmat.2009.10.107
关键词
Lysozyme; Anthraquinone dyes; Synchronous; Docking studies
资金
- CSIR [01(2217)/08/EMR-II]
- DST [SR/S5/NM- 16/2007]
- UGC [33-256/2007]
The interaction between lysozyme and anthraquinone dyes such as Alizarin Red S, Acid blue 129 and Uniblue was studied using steady state, time resolved fluorescence measurements and docking studies. Addition of anthraquinone dyes effectively quenched the intrinsic fluorescence of lysozyme. Fluorescence quenching of lysozyme by dyes has revealed the formation of complex. The number of binding sites (n) and binding constant (K) for all the three dyes was calculated by relevant fluorescence quenching data. Based on Forster's non-radiative energy transfer theory, distance (r(0)) between the donor (lysozyme) and acceptor(dyes) as well as the critical energy transfer distance (R-0) has also been calculated. The interaction between dyes and lysozyme Occurs through static quenching mechanism as confirmed by time resolved spectroscopy. The conformational change of lysozyme has been analyzed using synchronous fluorescence measurement. Finally, docking studies revealed that specific interactions were observed with the residue of Trp 62. (C) 2009 Elsevier B.V. All Fights reserved.
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