Buskirk Allen R, Liu David R
Department of Chemistry and Biochemistry, Brigham Young University, Provo, Utah 84602, USA.
Chem Biol. 2005 Feb;12(2):151-61. doi: 10.1016/j.chembiol.2004.11.012.
Biological small-molecule-dependent switches sense external chemical signals and transduce them into appropriate internal signals and cellular responses. Artificial molecular switches that control the function of any protein of interest using a small molecule are powerful tools for studying biology because they enable cellular responses to be controlled by inputs chosen by researcher. Furthermore, these switches can combine the generality of genetic regulation with the reversibility and temporal control afforded by small molecules. Three approaches to creating molecular switches include altering a natural switch to recognize new exogenous ligands, engineering novel allosteric responses to ligand binding, or enforcing protein localization with chemical dimerizers. Here, we discuss the development of small-molecule-dependent switches that control in a general fashion transcriptional activation, translational initiation, and protein activity posttranslationally.
生物小分子依赖性开关可感知外部化学信号,并将其转化为适当的内部信号和细胞反应。利用小分子控制任何感兴趣蛋白质功能的人工分子开关是研究生物学的强大工具,因为它们能使细胞反应受研究人员选择的输入控制。此外,这些开关可将基因调控的普遍性与小分子提供的可逆性和时间控制相结合。创建分子开关的三种方法包括改变天然开关以识别新的外源配体、设计对配体结合的新型变构反应,或用化学二聚体强制蛋白质定位。在此,我们讨论以通用方式控制转录激活、翻译起始和翻译后蛋白质活性的小分子依赖性开关的发展。