Fluorescence properties and photophysics of the sulfoindocyanine Cy3 linked covalently to DNA

被引:239
作者
Sanborn, Matthew E.
Connolly, Brian K.
Gurunathan, Kaushik
Levitus, Marcia [1 ]
机构
[1] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ 85287 USA
[2] Arizona State Univ, Dept Phys, Tempe, AZ 85287 USA
[3] Arizona State Univ, Biodesign Inst, Tempe, AZ 85287 USA
关键词
D O I
10.1021/jp072912u
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The sulfoindocyanine Cy3 is one of the most commonly used fluorescent dyes in the investigation of the structure and dynamics of nucleic acids by means of fluorescence methods. In this work, we report the fluorescence and photophysical properties of Cy3 attached covalently to single-stranded and duplex DNA. Steady-state and time-resolved fluorescence techniques were used to determine fluorescence quantum yields, emission lifetimes, and fluorescence anisotropy decays. The existence of a transient photoisomer was investigated by means of transient absorption techniques. The fluorescence quantum yield of Cy3 is highest when attached to the 5' terminus of single-stranded DNA (Cy3-5' ssDNA), and decreases by a factor of 2.4 when the complementary strand is annealed to form duplex DNA (Cy3-5' dsDNA). Substantial differences were also observed between the 5'-modified strands and strands modified through an internal amino-modified deoxy uridine. The fluorescence decay of Cy3 became multiexponential upon conjugation to DNA. The longest lifetime was observed for Cy3-5' ssDNA, where about 50% of the decay is dominated by a 2.0-ns lifetime. This value is more than 10 times larger than the fluorescence lifetime of the free dye in solution. These observations are interpreted in terms of a model where the molecule undergoes a trans-cis isomerization reaction from the first excited state. We observed that the activation energy for photoisomerization depends strongly on the microenvironment in which the dye is located. The unusually high activation energy measured for Cy3-5' ssDNA is an indication of dye-ssDNA interactions. In fact, the time-resolved fluorescence anisotropy decay of this sample is dominated by a 2.5-ns rotational correlation time, which evidences the lack of rotational freedom of the dye around the linker that separates it from the terminal 5' phosphate. The remarkable variations in the photophysical properties of Cy3-DNA constructs demonstrate that caution should be used when Cy3 is used in studies employing DNA conjugates.
引用
收藏
页码:11064 / 11074
页数:11
相关论文
共 47 条
[11]  
*CRC, 2006, CRC HDB CHEM PHYS
[12]   ORIENTATIONAL FREEDOM OF MOLECULAR PROBES - ORIENTATION FACTOR IN INTRA-MOLECULAR ENERGY-TRANSFER [J].
DALE, RE ;
EISINGER, J ;
BLUMBERG, WE .
BIOPHYSICAL JOURNAL, 1979, 26 (02) :161-193
[13]   Synthesis of fluorescently labelled oligonucleotides and nucleic acids [J].
Davies, MJ ;
Shah, A ;
Bruce, IJ .
CHEMICAL SOCIETY REVIEWS, 2000, 29 (02) :97-107
[14]   CONFORMATIONAL DISTRIBUTIONS OF A 4-WAY DNA JUNCTION REVEALED BY TIME-RESOLVED FLUORESCENCE RESONANCE ENERGY-TRANSFER [J].
EIS, PS ;
MILLAR, DP .
BIOCHEMISTRY, 1993, 32 (50) :13852-13860
[15]   Distortion of DNA junctions imposed by the binding of resolving enzymes: A fluorescence study [J].
Fogg, JM ;
Kvaratskhelia, M ;
White, MF ;
Lilley, DMJ .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 313 (04) :751-764
[16]   KINKING OF DNA AND RNA HELICES BY BULGED NUCLEOTIDES OBSERVED BY FLUORESCENCE RESONANCE ENERGY-TRANSFER [J].
GOHLKE, C ;
MURCHIE, AIH ;
LILLEY, DMJ ;
CLEGG, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (24) :11660-11664
[17]   EFFICIENCIES OF PHOTOINDUCED ELECTRON-TRANSFER REACTIONS - ROLE OF THE MARCUS INVERTED REGION IN RETURN ELECTRON-TRANSFER WITHIN GEMINATE RADICAL-ION PAIRS [J].
GOULD, IR ;
EGE, D ;
MOSER, JE ;
FARID, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (11) :4290-4301
[18]   Anomalous fluorescence enhancement of Cy3 and Cy3.5 versus anomalous fluorescence loss of Cy5 and Cy7 upon covalent linking to IgG and noncovalent binding to avidin [J].
Gruber, HJ ;
Hahn, CD ;
Kada, G ;
Riener, CK ;
Harms, GS ;
Ahrer, W ;
Dax, TG ;
Knaus, HG .
BIOCONJUGATE CHEMISTRY, 2000, 11 (05) :696-704
[19]   Single-molecule fluorescence resonance energy transfer [J].
Ha, T .
METHODS, 2001, 25 (01) :78-86
[20]   Photoinduced electron transfer between fluorescent dyes and guanosine residues in DNA-hairpins [J].
Heinlein, T ;
Knemeyer, JP ;
Piestert, O ;
Sauer, M .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (31) :7957-7964