Excited state reactions in fluorescent proteins

被引:274
作者
Meech, Stephen R. [1 ]
机构
[1] Univ E Anglia, Sch Chem, Norwich NR1 2QN, Norfolk, England
基金
英国工程与自然科学研究理事会;
关键词
BARRIER HYDROGEN-BONDS; EMISSION PH SENSORS; PHOTOINDUCED PEPTIDE CLEAVAGE; PROTON-TRANSFER; STRUCTURAL BASIS; GROUND-STATE; TEMPERATURE-DEPENDENCE; GFP-CHROMOPHORE; BIOLUMINESCENT PROTEIN; INTERNAL-CONVERSION;
D O I
10.1039/b820168b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The green fluorescent protein is a key technology in bioimaging. In this critical review, we consider how its various applications can be tailored from knowledge of the excited state chemistry. The photophysics of the basic chromophore in solution are described in detail, and the dominant radiationless decay mechanism is characterised. The quite different photophysics of wild type GFP are described next. The unique excited state proton transfer reaction observed can be used to model proton transfer processes in proteins. Examples where the proton transfer is blocked, or redirected to occur over a low short barrier H-bond are discussed. Finally the photophysics underlying the new generation of photochemically active fluorescent proteins are discussed (155 references).
引用
收藏
页码:2922 / 2934
页数:13
相关论文
共 156 条
[71]  
McAnaney TB, 2002, BIOPHYS J, V82, p314A
[72]   Green fluorescent protein variants as ratiometric dual emission pH sensors. 2. Excited-state dynamics [J].
McAnaney, TB ;
Park, ES ;
Hanson, GT ;
Remington, SJ ;
Boxer, SG .
BIOCHEMISTRY, 2002, 41 (52) :15489-15494
[73]   Green fluorescent protein variants as ratiometric dual emission pH sensors. 3. Temperature dependence of proton transfer [J].
McAnaney, TB ;
Shi, XH ;
Abbyad, P ;
Jung, H ;
Remington, SJ ;
Boxer, SG .
BIOCHEMISTRY, 2005, 44 (24) :8701-8711
[74]   Photophysics and Dihedral Freedom of the Chromophore in Yellow, Blue, and Green Fluorescent Protein [J].
Megley, Colleen M. ;
Dickson, Luisa A. ;
Maddalo, Scott L. ;
Chandler, Gabriel J. ;
Zimmer, Marc .
JOURNAL OF PHYSICAL CHEMISTRY B, 2009, 113 (01) :302-308
[75]   Dynamic and quantitative Ca2+ measurements using improved cameleons [J].
Miyawaki, A ;
Griesbeck, O ;
Heim, R ;
Tsien, RY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (05) :2135-2140
[76]   Fluorescent indicators for Ca2+ based on green fluorescent proteins and calmodulin [J].
Miyawaki, A ;
Llopis, J ;
Heim, R ;
McCaffery, JM ;
Adams, JA ;
Ikura, M ;
Tsien, RY .
NATURE, 1997, 388 (6645) :882-887
[77]   Visualization of the spatial and temporal dynamics of intracellular signaling [J].
Miyawaki, A .
DEVELOPMENTAL CELL, 2003, 4 (03) :295-305
[78]   Green fluorescent protein-like proteins in reef anthozoa animals [J].
Miyawaki, A .
CELL STRUCTURE AND FUNCTION, 2002, 27 (05) :343-347
[79]   Photo-induced peptide cleavage in the green-to-red conversion of a fluorescent protein [J].
Mizuno, H ;
Mal, TK ;
Tong, KI ;
Ando, R ;
Furuta, T ;
Ikura, M ;
Miyawakil, A .
MOLECULAR CELL, 2003, 12 (04) :1051-1058
[80]   Light-dependent regulation of structural flexibility in a photochromic fluorescent protein [J].
Mizuno, Hideaki ;
Mal, Tapas Kumar ;
Walchli, Markus ;
Kikuchi, Akihiro ;
Fukano, Takashi ;
Ando, Ryoko ;
Jeyakanthan, Jeyaraman ;
Taka, Junichiro ;
Shiro, Yoshitsugu ;
Ikura, Mitsuhiko ;
Miyawaki, Atsushi .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (27) :9227-9232