Lord Samuel J, Conley Nicholas R, Lee Hsiao-lu D, Samuel Reichel, Liu Na, Twieg Robert J, Moerner W E
Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA.
J Am Chem Soc. 2008 Jul 23;130(29):9204-5. doi: 10.1021/ja802883k. Epub 2008 Jun 24.
We have reengineered a red-emitting dicyanomethylenedihydrofuran push-pull fluorophore so that it is dark until photoactivated with a short burst of low-intensity violet light. Photoactivation of the dark fluorogen leads to conversion of an azide to an amine, which shifts the absorption to long wavelengths. After photoactivation, the fluorophore is bright and photostable enough to be imaged on the single-molecule level in living cells. This proof-of-principle demonstration provides a new class of bright photoactivatable fluorophores, as are needed for super-resolution imaging schemes that require active control of single molecule emission.
我们对一种发出红色荧光的二氰基亚甲基二氢呋喃推挽式荧光团进行了重新设计,使其在被短脉冲低强度紫光光激活之前处于暗态。暗态荧光原的光激活会导致叠氮化物转化为胺,从而使吸收峰移至长波长处。光激活后,该荧光团亮度足够高且光稳定性良好,足以在活细胞的单分子水平上进行成像。这一原理验证演示提供了一类新型的明亮光激活荧光团,这是需要对单分子发射进行主动控制的超分辨率成像方案所必需的。