Steady-state and time-resolved spectroscopic studies of green-to-red photoconversion of fluorescent protein Dendra2

被引:12
|
作者
Makarov, Nikolay S. [1 ,2 ]
Cirloganu, Claudiu [1 ,2 ]
Perry, Joseph W. [1 ,2 ]
Lukyanov, Konstantin A. [3 ]
Solntsev, Kyril M. [1 ,2 ]
机构
[1] Georgia Inst Technol, Sch Chem & Biochem, 901 Atlantic Dr, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, Ctr Organ Photon & Elect, Atlanta, GA 30332 USA
[3] Russian Acad Sci, Inst Bioorgan Chem, Moscow 117997, Russia
基金
俄罗斯基础研究基金会; 美国国家科学基金会;
关键词
Fluorescent Proteins; Photoconversion; Dendra2; Transient absorption; PHOTOINDUCED PEPTIDE CLEAVAGE; STRUCTURAL BASIS; CONVERSION; KAEDE; CHROMOPHORE; MICROSCOPY; MECHANISM; UV; LOCALIZATION; ABSORPTION;
D O I
10.1016/j.jphotochem.2014.02.001
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
The excited state dynamics and green-to-red photoconversion (PC) of the monomer fluorescent protein Dendra2 were studied using time resolved pump-probe and double-pulsed excitation experiments. A linear dependence of the PC efficiency on the pump power is demonstrated when exciting the neutral green form at 400 nm as well as anionic green form at either 458 or 488 nm. Rather large PC quantum yields of similar to 1.5 x 10(-3) for the neutral form and similar to 6 x 10(-5) for the anionic form are determined from exposuredependent PC saturation experiments. At the same time, no dependence of the PC rate on the time delay between the pulses is observed, as well as no significant difference between PC via pulsed or continuous-wave (ON) excitation. Our wavelength- and pH-dependent studies of the PC process suggest that the Dendra2 green-to-red conversion occurs following the absorption of one photon, directly from the excited state of each (neutral and anionic) form of the green protein without intermediate excited states or species requiring absorption of additional photons. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:5 / 13
页数:9
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