Biologically active molecules with a "light switch"

被引:962
作者
Mayer, Guenter [1 ]
Heckel, Alexander [1 ]
机构
[1] Univ Bonn, Kekule Inst Organ Chem & Biochem, D-53121 Bonn, Germany
关键词
bioorganic chemistry; caged compounds; photochemistry; photoswitches; protecting groups;
D O I
10.1002/anie.200600387
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Biologically active compounds which are light-responsive offer experimental possibilities which are otherwise very difficult to achieve. Since light can be manipulated very precisely, for example, with lasers and microscopes rapid jumps in concentration of the active form of molecules are possible with exact control of the area, time, and dosage. The development of such strategies started in the 1970s. This review summarizes new developments of the last five years and deals with "small molecules", proteins, and nucleic acids which can either be irreversibly activated with light (these compounds are referred to as "caged compounds") or reversibly switched between an active and an inactive state. © 2006 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:4900 / 4921
页数:22
相关论文
共 276 条
[51]   Light signal transduction in higher plants [J].
Chen, M ;
Chory, J ;
Fankhauser, C .
ANNUAL REVIEW OF GENETICS, 2004, 38 :87-117
[52]   Photolysis of γ-(α-carboxy-2-nitrobenzyl)-L-glutamic acid investigated in the microsecond time scale by time-resolved FTIR [J].
Cheng, Q ;
Steinmetz, MG ;
Jayaraman, V .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (26) :7676-7677
[53]  
Cho-Chung YS, 1999, CURR OPIN MOL THER, V1, P386
[54]   S-pixyl analogues as photocleavable protecting groups for nucleosides [J].
Coleman, MP ;
Boyd, MK .
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (22) :7641-7648
[55]   New phototriggers:: Extending the p-hydroxyphenacyl π-π* absorption range [J].
Conrad, PG ;
Givens, RS ;
Weber, JFW ;
Kandler, K .
ORGANIC LETTERS, 2000, 2 (11) :1545-1547
[56]   Photolytic cleavage of 1-(2-nitrophenyl)ethyl ethers involves two parallel pathways and product release is rate-limited by decomposition of a common hemiacetal intermediate [J].
Corrie, JET ;
Barth, A ;
Munasinghe, VRN ;
Trentham, DR ;
Hutter, MC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (28) :8546-8554
[57]   3-Nitro-3-deaza-2'-deoxyadenosine as a versatile photocleavable 2'-deoxyadenosine mimic [J].
Crey-Desbiolles, C ;
Lhomme, J ;
Dumy, P ;
Kotera, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (31) :9532-9533
[58]   Antisense strategies [J].
Crooke, ST .
CURRENT MOLECULAR MEDICINE, 2004, 4 (05) :465-487
[59]   Light-activated gene expression [J].
Cruz, FG ;
Koh, JT ;
Link, KH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (36) :8777-8778
[60]   Synthesis and biochemical properties of a new photoactivatable cholesterol analog 7,7-azocholestanol and its linoleate ester in Chinese hamster ovary cell lines [J].
Cruz, JC ;
Thomas, M ;
Wong, E ;
Ohgami, N ;
Sugii, S ;
Curphey, T ;
Chang, CCY ;
Chang, TY .
JOURNAL OF LIPID RESEARCH, 2002, 43 (08) :1341-1347