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本文引用的文献

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Coherent control of bond breaking in amino acid complexes with tailored femtosecond pulses.
J Chem Phys. 2007 Nov 28;127(20):201101. doi: 10.1063/1.2806029.
2
Excited states of GFP chromophore and active site studied by the SAC-CI method: effect of protein-environment and mutations.用SAC-CI方法研究绿色荧光蛋白发色团和活性位点的激发态:蛋白质环境和突变的影响。
J Comput Chem. 2007 Nov 30;28(15):2443-52. doi: 10.1002/jcc.20667.
3
Enhancement of the fluorescence of the blue fluorescent proteins by high pressure or low temperature.通过高压或低温增强蓝色荧光蛋白的荧光。
J Phys Chem B. 2005 Jul 7;109(26):12976-81. doi: 10.1021/jp0448595.
4
Fourier transform measurement of two-photon excitation spectra: applications to microscopy and optimal control.双光子激发光谱的傅里叶变换测量:在显微镜学和最优控制中的应用
Opt Lett. 2005 Apr 15;30(8):911-3. doi: 10.1364/ol.30.000911.
5
Characterization of two-photon excitation fluorescence lifetime imaging microscopy for protein localization.用于蛋白质定位的双光子激发荧光寿命成像显微镜的特性研究
Microsc Res Tech. 2004 Jan 1;63(1):72-80. doi: 10.1002/jemt.10430.
6
Attenuation of photobleaching in two-photon excitation fluorescence from green fluorescent protein with shaped excitation pulses.通过整形激发脉冲减弱绿色荧光蛋白双光子激发荧光中的光漂白现象。
Biochem Biophys Res Commun. 2003 Nov 21;311(3):592-6. doi: 10.1016/j.bbrc.2003.09.236.
7
The use of FRET imaging microscopy to detect protein-protein interactions and protein conformational changes in vivo.利用荧光共振能量转移成像显微镜在体内检测蛋白质-蛋白质相互作用和蛋白质构象变化。
Curr Opin Struct Biol. 2001 Oct;11(5):573-8. doi: 10.1016/s0959-440x(00)00249-9.
8
Photoselective adaptive femtosecond quantum control in the liquid phase.液相中的光选择性自适应飞秒量子控制
Nature. 2001 Nov 1;414(6859):57-60. doi: 10.1038/35102037.
9
Shedding light on the dark and weakly fluorescent states of green fluorescent proteins.揭示绿色荧光蛋白的暗态和弱荧光态
Proc Natl Acad Sci U S A. 1999 May 25;96(11):6177-82. doi: 10.1073/pnas.96.11.6177.
10
Using GFP in FRET-based applications.
Trends Cell Biol. 1999 Feb;9(2):57-60. doi: 10.1016/s0962-8924(98)01434-2.

利用先进的进化脉冲整形技术对蓝色荧光蛋白进行控制。

Control of the blue fluorescent protein with advanced evolutionary pulse shaping.

作者信息

Tkaczyk Eric R, Mauring Koit, Tkaczyk Alan H, Krasnenko Veera, Ye Jing Yong, Baker James R, Norris Theodore B

机构信息

Center for Ultrafast Optical Science, University of Michigan, 2200 Bonisteel Boulevard, Ann Arbor, MI 48109-2099, USA.

出版信息

Biochem Biophys Res Commun. 2008 Nov 28;376(4):733-7. doi: 10.1016/j.bbrc.2008.09.075. Epub 2008 Sep 24.

DOI:10.1016/j.bbrc.2008.09.075
PMID:18817751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2600451/
Abstract

We demonstrate optical coherent control of the two-photon fluorescence of the blue fluorescent protein (BFP), which is of interest in investigations of protein-protein interactions. In addition to biological relevance, BFP represents an interesting target for coherent control from a chemical perspective due to its many components of highly nonexponential fluorescence decay and low quantum yield resulting from excited state isomerization. Using a genetic algorithm with a multiplicative (rather than ratiometric) fitness parameter, we are able to control the ratio of BFP fluorescence to second-harmonic generation without a considerable drop in the maximized signal. The importance of linear chirp and power-scaling on the discrimination process is investigated in detail.

摘要

我们展示了对蓝色荧光蛋白(BFP)双光子荧光的光学相干控制,这在蛋白质 - 蛋白质相互作用研究中具有重要意义。除了生物学相关性外,从化学角度来看,BFP也是相干控制的一个有趣目标,因为它具有许多高度非指数荧光衰减的成分,并且由于激发态异构化导致量子产率较低。使用具有乘法(而非比例)适应度参数的遗传算法,我们能够控制BFP荧光与二次谐波产生的比率,同时最大化信号不会有显著下降。详细研究了线性啁啾和功率缩放对鉴别过程的重要性。