Blue fluorescent dye-protein complexes based on fluorogenic cyanine dyes and single chain antibody fragments

被引:50
作者
Zanotti, Kimberly J. [1 ]
Silva, Gloria L. [1 ]
Creeger, Yehuda [3 ,4 ]
Robertson, Kelly L. [1 ]
Waggoner, Alan S. [2 ,3 ,4 ]
Berget, Peter B. [2 ,3 ,4 ]
Armitage, Bruce A. [1 ,3 ,4 ]
机构
[1] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Biol Sci, Pittsburgh, PA 15213 USA
[3] Carnegie Mellon Univ, Dept Mol Biosensor, Pittsburgh, PA 15213 USA
[4] Carnegie Mellon Univ, Imaging Ctr, Pittsburgh, PA 15213 USA
基金
美国国家卫生研究院;
关键词
PHOTOSTABILITY; FLUOROMODULES; GENE; DNA;
D O I
10.1039/c0ob00444h
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Fluoromodules are complexes formed upon the noncovalent binding of a fluorogenic dye to its cognate biomolecular partner, which significantly enhances the fluorescence quantum yield of the dye. Previously, several single-chain, variable fragment (scFv) antibodies were selected from a yeast cell surface-displayed library that activated fluorescence from a family of unsymmetrical cyanine dyes covering much of the visible and near-IR spectrum. The current work expands our repertoire of genetically encodable scFv-dye pairs by selecting and characterizing a group of scFvs that activate fluorogenic violet-absorbing, blue-fluorescing cyanine dyes, based on oxazole and thiazole heterocycles. The dye binds to both yeast cell surface-displayed and soluble scFvs with low nanomolar K-d values. These dye-protein fluoromodules exhibit high quantum yields, approaching unity for the brightest system. The promiscuity of these scFvs with other fluorogenic cyanine dyes was also examined. Fluorescence microscopy demonstrates that the yeast cell surface-displayed scFvs can be used for multicolor imaging. The prevalence of 405 nm lasers on confocal imaging and flow cytometry systems make these new reagents potentially valuable for cell biological studies.
引用
收藏
页码:1012 / 1020
页数:9
相关论文
共 30 条
[1]   Exploration of new chromophore structures leads to the identification of improved blue fluorescent proteins [J].
Ai, Hui-wang ;
Shaner, Nathan C. ;
Cheng, Zihao ;
Tsien, Roger Y. ;
Campbell, Robert E. .
BIOCHEMISTRY, 2007, 46 (20) :5904-5910
[2]   GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION [J].
CHALFIE, M ;
TU, Y ;
EUSKIRCHEN, G ;
WARD, WW ;
PRASHER, DC .
SCIENCE, 1994, 263 (5148) :802-805
[3]   Isolating and engineering human antibodies using yeast surface display [J].
Chao, Ginger ;
Lau, Wai L. ;
Hackel, Benjamin J. ;
Sazinsky, Stephen L. ;
Lippow, Shaun M. ;
Wittrup, K. Dane .
NATURE PROTOCOLS, 2006, 1 (02) :755-768
[4]   Synthesis of new fluorogenic cyanine dyes and incorporation into RNA fluoromodules [J].
Constantin, Tudor P. ;
Silva, Gloria L. ;
Robertson, Kelly L. ;
Hamilton, Tamara P. ;
Fague, Kaitlin ;
Waggoner, Alan S. ;
Armitage, Bruce A. .
ORGANIC LETTERS, 2008, 10 (08) :1561-1564
[5]  
Creeger Y., UNPUB
[6]   Deeply inverted electron-hole recombination in a luminescent antibody-stilbene complex [J].
Debler, Erik W. ;
Kaufmann, Gunnar F. ;
Meijler, Michael M. ;
Heine, Andreas ;
Mee, Jenny M. ;
Pljevaljcic, Goran ;
Di Bilio, Angel J. ;
Schultz, Peter G. ;
Millar, David P. ;
Janda, Kim D. ;
Wilson, Ian A. ;
Gray, Harry B. ;
Lerner, Richard A. .
SCIENCE, 2008, 319 (5867) :1232-1235
[7]  
Deligeorgiev Todor G., 2009, Recent Patents on Materials Science, V2, P1, DOI 10.2174/1874465610902010001
[8]   ScFv-based fluorogen activating proteins and variable domain inhibitors as fluorescent biosensor platforms [J].
Department of Biological Sciences, Molecular Biosensor and Imaging Center, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, PA 15213, United States ;
不详 .
Biotechnol. J., 2009, 9 (1328-1336) :1328-1336
[9]   Flow-cytometric isolation of human antibodies from a nonimmune Saccharomyces cerevisiae surface display library [J].
Feldhaus, MJ ;
Siegel, RW ;
Opresko, LK ;
Coleman, JR ;
Feldhaus, JMW ;
Yeung, YA ;
Cochran, JR ;
Heinzelman, P ;
Colby, D ;
Swers, J ;
Graff, C ;
Wiley, HS ;
Wittrup, KD .
NATURE BIOTECHNOLOGY, 2003, 21 (02) :163-170
[10]   STED Nanoscopy in Living Cells Using Fluorogen Activating Proteins [J].
Fitzpatrick, James A. J. ;
Yan, Qi ;
Sieber, Jochen J. ;
Dyba, Marcus ;
Schwarz, Ulf ;
Szent-Gyorgyi, Chris ;
Woolford, Carol A. ;
Berget, Peter B. ;
Waggoner, Alan S. ;
Bruchez, Marcel P. .
BIOCONJUGATE CHEMISTRY, 2009, 20 (10) :1843-1847