Fluorescence dynamics of green fluorescent protein in AOT reversed micelles

被引:47
作者
Uskova, MA
Borst, JW
Hink, MA
van Hoek, A
Schots, A
Klyachko, NL
Visser, AJWG
机构
[1] Univ Wageningen & Res Ctr, Dept Biomol Sci, Microspect Ctr, NL-7603 HA Wageningen, Netherlands
[2] Moscow MV Lomonosov State Univ, Fac Chem, Dept Chem Enzymol, Moscow 119899, Russia
[3] Univ Wageningen & Res Ctr, Dept Plant Sci, Lab Monoclonal Antibodies, NL-6709 PD Wageningen, Netherlands
关键词
green fluorescent protein; reversed micelles; AOT; water droplets; time-resolved fluorescence;
D O I
10.1016/S0301-4622(00)00184-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have used the enhanced green fluorescent protein (EGFP) to investigate the properties of surfactant-entrapped water pools in organic solvents (reversed micelles) with steady-state and time-resolved fluorescence methods. The surfactant used was sodium bis(2-ethylhexyl)sulfosuccinate (AOT) and the organic solvents were isooctane and (the more viscous) dodecane, respectively. The water content of the water pools could be controlled through the parameter w(0), which is the water-to-surfactant molar ratio. With steady-state fluorescence, it was observed that subtle fluorescence changes could be noted in reversed micelles of different water contents. EGFP can be used as a pH-indicator of the water droplets in reversed micelles. Time-resolved fluorescence methods also revealed subtle changes in fluorescence decay times when the results in bulk water were compared with those in reversed micelles. The average fluorescence lifetimes of EGFP scaled with the relative fluorescence intensities. Time-resolved fluorescence anisotropy of EGFP in aqueous solution and reversed micelles yielded single rotational correlation times. Geometrical considerations could assign the observed correlation times to dehydrated protein at low w(0) and internal EGFP rotation within the droplet at the highest w(0). (C) 2000 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:73 / 84
页数:12
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