Mayer Günter, Heckel Alexander
Kekulé-Institut für Organische Chemie und Biochemie, Rheinische Friedrich-Wilhelms-Universität Bonn, Gerhard-Domagk-Strasse 1, 53121 Bonn, Germany.
Angew Chem Int Ed Engl. 2006 Jul 24;45(30):4900-21. doi: 10.1002/anie.200600387.
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.
具有光响应性的生物活性化合物提供了一些实验可能性,而这些可能性用其他方法很难实现。例如,由于光可以通过激光和显微镜进行非常精确的操控,因此能够在精确控制作用区域、时间和剂量的情况下,使分子活性形式的浓度迅速跃升。这类策略的研发始于20世纪70年代。本综述总结了过去五年的新进展,并涉及可被光不可逆激活的“小分子”、蛋白质和核酸(这些化合物被称为“笼形化合物”),或可在活性状态与非活性状态之间可逆转换的物质。