Photoswitched DNA-binding of a photochromic spiropyran

被引:175
作者
Andersson, Johanna [1 ]
Li, Shiming [1 ]
Lincoln, Per [1 ]
Andreasson, Joakim [1 ]
机构
[1] Chalmers Univ Technol, Dept Biol & Chem Engn, SE-41296 Gothenburg, Sweden
基金
瑞典研究理事会;
关键词
D O I
10.1021/ja801968f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The dramatically different DNA-binding properties of the two isomeric forms of a photochromic spiropyran have been demonstrated, enabling photoswitched DNA binding. The closed, UV-absorbing form shows no signs of interaction with DNA. Upon UV exposure the spiropyran is isomerized to the open form that binds to DNA by intercalation. The process is fully reversible as the corresponding dissociation process is induced by visible light. Copyright © 2008 American Chemical Society.
引用
收藏
页码:11836 / 11837
页数:2
相关论文
共 21 条
[11]   Photoregulation of RNA digestion by RNase H with azobenzene-tethered DNA [J].
Matsunaga, D ;
Asanuma, H ;
Komiyama, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (37) :11452-11453
[12]   Biologically active molecules with a "light switch" [J].
Mayer, Guenter ;
Heckel, Alexander .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (30) :4900-4921
[13]   Non-covalent ligand/DNA interactions: Minor groove binding agents [J].
Nelson, Stephanie M. ;
Ferguson, Lynnette R. ;
Denny, William A. .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2007, 623 (1-2) :24-40
[14]   2′,6′-Dimethylazobenzene as an efficient and thermo-stable photo-regulator for the photoregulation of DNA hybridization [J].
Nishioka, Hidenori ;
Liang, Xingguo ;
Kashida, Hiromu ;
Asanuma, Hiroyuki .
CHEMICAL COMMUNICATIONS, 2007, (42) :4354-4356
[15]   HIGH-SENSITIVITY LINEAR DICHROISM AS A TOOL FOR EQUILIBRIUM-ANALYSIS IN BIOCHEMISTRY - STABILITY CONSTANT OF DNA-ETHIDIUMBROMIDE COMPLEX [J].
NORDEN, B ;
TJERNELD, F .
BIOPHYSICAL CHEMISTRY, 1976, 4 (02) :191-198
[16]   LINEAR DICHROISM SPECTROSCOPY OF NUCLEIC-ACIDS [J].
NORDEN, B ;
KUBISTA, M ;
KURUCSEV, T .
QUARTERLY REVIEWS OF BIOPHYSICS, 1992, 25 (01) :51-170
[17]   Comprehensive theoretical study of the conversion reactions of spiropyrans: Substituent and solvent effects [J].
Sheng, YH ;
Leszczynski, J ;
Garcia, AA ;
Rosario, R ;
Gust, D ;
Springer, J .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (41) :16233-16243
[18]   Photoswitchable biomaterials: En route to optobioelectronic systems [J].
Willner, I .
ACCOUNTS OF CHEMICAL RESEARCH, 1997, 30 (09) :347-356
[19]   Excited-state dynamics of spiropyran-derived merocyanine isomers [J].
Wohl, CJ ;
Kuciauskas, D .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (47) :22186-22191
[20]  
Yamazawa A, 2000, ANGEW CHEM INT EDIT, V39, P2356, DOI 10.1002/1521-3773(20000703)39:13<2356::AID-ANIE2356>3.0.CO