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荧光标记蛋白EosFP的靶向绿-红光电转换

Targeted Green-Red Photoconversion of EosFP, a Fluorescent Marker Protein.

作者信息

Ivanchenko Sergey, Röcker Carlheinz, Oswald Franz, Wiedenmann Jörg, Nienhaus G Ulrich

机构信息

Department of Biophysics, University of Ulm, 89069 Ulm, Germany.

出版信息

J Biol Phys. 2005 Dec;31(3-4):249-59. doi: 10.1007/s10867-005-0174-z.

Abstract

EosFP is a novel fluorescent protein from the stony coral Lobophyllia hemprichii. Its gene was cloned in Escherichia coli to express the tetrameric wild-type protein. The protein emits strong green fluorescence (516 nm) that shifts toward red (581 nm) upon near-ultraviolet irradiation at ∼390 nm due to a photo-induced modification that involves a break in the peptide backbone next to the chromophore. Using site-directed mutagenesis, dimeric (d1EosFP, d2EosFP) and monomeric (mEosFP) variants were produced with essentially unaltered spectroscopic properties. Here we present a spectroscopic characterization of EosFP and its variants, including room- and low-temperature spectra, fluorescence lifetime determinations, two-photon excitation and two-photon photoconversion. Furthermore, by transfection of a human cancer (HeLa) cell with a fusion construct of a mitochondrial targeting sequence and d2EosFP, we demonstrate how localized photoconversion of EosFP can be employed for resolving intracellular processes.

摘要

EosFP是一种来自石珊瑚赫氏叶状珊瑚(Lobophyllia hemprichii)的新型荧光蛋白。其基因在大肠杆菌中克隆以表达四聚体野生型蛋白。该蛋白发出强烈的绿色荧光(516nm),在约390nm的近紫外光照射下,由于一种光诱导修饰,荧光会向红色(581nm)移动,这种修饰涉及发色团旁边肽主链的断裂。利用定点诱变技术,制备了具有基本未改变光谱特性的二聚体(d1EosFP、d2EosFP)和单体(mEosFP)变体。在此,我们展示了EosFP及其变体的光谱特征,包括室温及低温光谱、荧光寿命测定、双光子激发和双光子光转化。此外,通过用线粒体靶向序列与d2EosFP的融合构建体转染人癌细胞(HeLa),我们展示了如何利用EosFP的局部光转化来解析细胞内过程。

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