Author:
Zheng Ying,Ye Zhiwei,Zhang Xue,Xiao Yi
Abstract
AbstractSuper-resolution imaging in a single-molecule localization approach has transformed the bulk fluorescence requirements to a single-molecule level, raising a revolution in the fluorophore engineering. Yet, it is a challenge to structurally devise fluorophores manipulating the single-molecule blinking kinetics. In this pursuit, we have developed a new strategy by innovatively integrating the photoactivatable nitroso-caging strategy into self-blinking sulfonamide, to forming a nitroso-caged sulfonamide rhodamine (NOSR). Our fluorophore demonstrated controllable self-blinking events upon photo-triggered uncaging release. This exceptional blink kinetics improved integrity in super-resolution imaging microtubules compared to self-blinking analogues. With the aid of paramount single-molecule fluorescence kinetics, we successfully reconstructed the axial morphology of mitochondrial outer membranes. We foresee that our synthetic approach of photoactivation and self-blinking would set a new avenue for devising rhodamines for super-resolution imaging.Abstract Figure
Publisher
Cold Spring Harbor Laboratory