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
[1]   Semiconductor nanocrystals as fluorescent biological labels [J].
Bruchez, M ;
Moronne, M ;
Gin, P ;
Weiss, S ;
Alivisatos, AP .
SCIENCE, 1998, 281 (5385) :2013-2016
[2]   Quantum dot bioconjugates for ultrasensitive nonisotopic detection [J].
Chan, WCW ;
Nie, SM .
SCIENCE, 1998, 281 (5385) :2016-2018
[3]   Capping of CdSe-ZnS quantum dots with DHLA and subsequent conjugation with proteins [J].
Clapp, Aaron R. ;
Goldman, Ellen R. ;
Mattoussi, Hedi .
NATURE PROTOCOLS, 2006, 1 (03) :1258-1266
[4]   Fluorescence resonance energy transfer between quantum dot donors and dye-labeled protein acceptors [J].
Clapp, AR ;
Medintz, IL ;
Mauro, JM ;
Fisher, BR ;
Bawendi, MG ;
Mattoussi, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (01) :301-310
[5]   Forster resonance energy transfer investigations using quantum-dot fluorophores [J].
Clapp, AR ;
Medintz, IL ;
Mattoussi, H .
CHEMPHYSCHEM, 2006, 7 (01) :47-57
[6]   Quantum dot-based multiplexed fluorescence resonance energy transfer [J].
Clapp, AR ;
Medintz, IL ;
Uyeda, HT ;
Fisher, BR ;
Goldman, ER ;
Bawendi, MG ;
Mattoussi, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (51) :18212-18221
[7]   OBSERVING THE HELICAL GEOMETRY OF DOUBLE-STRANDED DNA IN SOLUTION BY FLUORESCENCE RESONANCE ENERGY-TRANSFER [J].
CLEGG, RM ;
MURCHIE, AIH ;
ZECHEL, A ;
LILLEY, DMJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) :2994-2998
[8]   PhotochemCAD: A computer-aided design and research tool in photochemistry [J].
Du, H ;
Fuh, RCA ;
Li, JZ ;
Corkan, LA ;
Lindsey, JS .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1998, 68 (02) :141-142
[9]   A new method for the isolation of histatins 1, 3, and 5 from parotid secretion using zinc precipitation [J].
Flora, B ;
Gusman, H ;
Helmerhorst, EJ ;
Troxler, RF ;
Oppenheim, FG .
PROTEIN EXPRESSION AND PURIFICATION, 2001, 23 (01) :198-206
[10]   Three-chromophore FRET microscopy to analyze multiprotein interactions in living cells [J].
Galperin, E ;
Verkhusha, V ;
Sorkin, A .
NATURE METHODS, 2004, 1 (03) :209-217