Grimm Jonathan B, Gruber Todd D, Ortiz Gloria, Brown Timothy A, Lavis Luke D
Janelia Research Campus, Howard Hughes Medical Institute , 19700 Helix Drive, Ashburn, Virginia 20147, United States.
Bioconjug Chem. 2016 Feb 17;27(2):474-80. doi: 10.1021/acs.bioconjchem.5b00566. Epub 2015 Dec 22.
Fluorogenic molecules are important tools for biological and biochemical research. The majority of fluorogenic compounds have a simple input-output relationship, where a single chemical input yields a fluorescent output. Development of new systems where multiple inputs converge to yield an optical signal could refine and extend fluorogenic compounds by allowing greater spatiotemporal control over the fluorescent signal. Here, we introduce a new red-shifted fluorescein derivative, Virginia Orange, as an exceptional scaffold for single- and dual-input fluorogenic molecules. Unlike fluorescein, installation of a single masking group on Virginia Orange is sufficient to fully suppress fluorescence, allowing preparation of fluorogenic enzyme substrates with rapid, single-hit kinetics. Virginia Orange can also be masked with two independent moieties; both of these masking groups must be removed to induce fluorescence. This allows facile construction of multi-input fluorogenic probes for sophisticated sensing regimes and genetic targeting of latent fluorophores to specific cellular populations.
荧光分子是生物和生化研究的重要工具。大多数荧光化合物具有简单的输入-输出关系,即单一化学输入产生荧光输出。开发新的系统,使多个输入汇聚以产生光信号,可以通过对荧光信号进行更大的时空控制来改进和扩展荧光化合物。在这里,我们引入一种新的红移荧光素衍生物弗吉尼亚橙,作为单输入和双输入荧光分子的优异支架。与荧光素不同,在弗吉尼亚橙上安装单个掩蔽基团就足以完全抑制荧光,从而能够制备具有快速单步动力学的荧光酶底物。弗吉尼亚橙也可以用两个独立的部分进行掩蔽;必须去除这两个掩蔽基团才能诱导荧光。这使得能够轻松构建用于复杂传感机制的多输入荧光探针,并将潜在荧光团基因靶向特定细胞群体。