Self-assembled donor comprising quantum dots and fluorescent proteins for long-range fluorescence resonance energy transfer

被引:115
作者
Lu, Huachang [1 ]
Schoeps, Oliver [2 ]
Woggon, Ulrike [2 ]
Niemeyer, Christof M. [1 ]
机构
[1] Tech Univ Dortmund, Fak Chem Biol Chem Mikrostrukturtech, D-44227 Dortmund, Germany
[2] Tech Univ Dortmund, Fak Phys, D-44227 Dortmund, Germany
关键词
D O I
10.1021/ja078243f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report on the development of a self-assembled donor for long-range fluorescence resonance energy transfer (FRET). To this end, a three-chromophore FRET (3Ch-FRET) system was constructed, which consists of a luminescent quantum dot (QD), enhanced yellow fluorescent proteins (EYFP), and Atto647-dye-modified oligonucleotides. The system was assembled by electrostatic binding of covalent EYFP-ssDNA conjugate to the QD and subsequent hybridization with complementary oligonucleotides labeled with Atto647-dye. The final conjugates comprise three different two-chromophore FRET (2Ch-FRET) subsystems, QD/EYFP, OD/Atto647, and EYFP/Atto647, respectively, which were studied in detail by steady-state and time-resolved photoluminescence measurements. The helicity of DNA allowed us to control donor/acceptor separations and thus enabled the detailed analysis of the various FRET processes. We found that the 2Ch-FRET and the 3Ch-FRET (QD/EYFP/Atto647) systems revealed FRET efficiencies and transfer rates that were affected by the availability of distinct FRET pathways. The derived energy-transfer efficiencies and Forster radii indicated that within the 3Ch-FRET system, the 2Ch-FRET subsystem QD/EYFP showed highest FRET efficiencies ranging from 64 to 72%. Thus, it can be used as a powerful donor system that combines the intrinsic advantages of QDs (large and spectrally broad absorption cross section) and EYFP (high quantum yield) and enables long-distance FRET processes for donor-acceptor distances of up to 13 nm.
引用
收藏
页码:4815 / 4827
页数:13
相关论文
共 47 条
[11]   Lipid-coated nanocrystals as multifunctionalized luminescent scaffolds for supramolecular biological assemblies [J].
Geissbuehler, I ;
Hovius, R ;
Martinez, KL ;
Adrian, M ;
Thampi, KR ;
Vogel, H .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (09) :1388-1392
[12]   A hybrid quantum dot-antibody fragment fluorescence resonance energy transfer-based TNT sensor [J].
Goldman, ER ;
Medintz, IL ;
Whitley, JL ;
Hayhurst, A ;
Clapp, AR ;
Uyeda, HT ;
Deschamps, JR ;
Lassman, ME ;
Mattoussi, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (18) :6744-6751
[13]   Binding of muscimol-conjugated quantum dots to GABAc receptors [J].
Gussin, Helene A. ;
Tomlinson, Ian D. ;
Little, Deborah M. ;
Warnement, Michael R. ;
Qian, Haohua ;
Rosenthal, Sandra J. ;
Pepperberg, David R. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (49) :15701-15713
[14]   Triple FRET: A tool for studying long-range molecular interactions [J].
Haustein, E ;
Jahnz, M ;
Schwille, P .
CHEMPHYSCHEM, 2003, 4 (07) :745-748
[15]   Multistep energy transfer in single molecular photonic wires [J].
Heilemann, M ;
Tinnefeld, P ;
Mosteiro, GS ;
Garcia-Parajo, M ;
Van Hulst, NF ;
Sauer, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (21) :6514-6515
[16]   Energy transfer between CdSe/ZnS Core/Shell quantum dots and fluorescent proteins [J].
Hering, Vitor R. ;
Gibson, Gary ;
Schumacher, Robert I. ;
Faljoni-Alario, Adelaide ;
Politi, Mario J. .
BIOCONJUGATE CHEMISTRY, 2007, 18 (06) :1705-1708
[17]   Synthesis and characterization of strongly luminescing ZnS-Capped CdSe nanocrystals [J].
Hines, MA ;
Guyot-Sionnest, P .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (02) :468-471
[18]   Sequential multistep energy transfer: enhancement of efficiency of long-range fluorescence resonance energy transfer [J].
Kawahara, S ;
Uchimaru, T ;
Murata, S .
CHEMICAL COMMUNICATIONS, 1999, (06) :563-564
[19]   Adaptation of inorganic quantum dots for stable molecular beacons [J].
Kim, JH ;
Morikis, D ;
Ozkan, M .
SENSORS AND ACTUATORS B-CHEMICAL, 2004, 102 (02) :315-319
[20]   A three-fluorophore FRET assay for high-throughput screening of small-molecule inhibitors of ribosome assembly [J].
Klostermeier, D ;
Sears, P ;
Wong, CH ;
Millar, DP ;
Williamson, JR .
NUCLEIC ACIDS RESEARCH, 2004, 32 (09) :2707-2715