Jusuk Ija, Vietz Carolin, Raab Mario, Dammeyer Thorben, Tinnefeld Philip
Institute for Physical &Theoretical Chemistry, and Braunschweig Integrated Centre of Systems Biology (BRICS), and Laboratory for Emerging Nanometrology (LENA), Braunschweig University of Technology, Braunschweig 38106, Germany.
Sci Rep. 2015 Sep 16;5:14075. doi: 10.1038/srep14075.
Photostability is one of the crucial properties of a fluorophore which strongly influences the quality of single molecule-based super-resolution imaging. Enhanced yellow fluorescent protein (eYFP) is one of the most widely used versions of fluorescent proteins in modern cell biology exhibiting fast intrinsic blinking and reversible photoactivation by UV light. Here, we developed an assay for studying photostabilization of single eYFP molecules with respect to fast blinking and demonstrated a 6-fold enhanced photostability of single eYFP molecules with a beneficial influence on the blinking kinetics under oxygen removal and addition of aliphatic thiols (dSTORM-buffer). Conjugation to single stranded DNA and immobilization via DNA hybridization on a DNA origami 12 helix bundle in aqueous solution allowed photophyiscal studies of eYFP at the single-molecule level and at close to physiological conditions. The benefit of improved photophysical properties for localization-based super-resolution microscopy is demonstrated and quantitatively characterized by imaging 12 helix bundle DNA origami nanorulers with binding sites at designed distances of 160 and 100 nm and by imaging microtubules in fixed mammalian Vero cells.
光稳定性是荧光团的关键特性之一,它对基于单分子的超分辨率成像质量有很大影响。增强型黄色荧光蛋白(eYFP)是现代细胞生物学中使用最广泛的荧光蛋白版本之一,具有快速的固有闪烁特性,并能被紫外光可逆光激活。在此,我们开发了一种用于研究单个eYFP分子在快速闪烁方面光稳定性的测定方法,并证明在去除氧气和添加脂肪族硫醇(dSTORM缓冲液)的情况下,单个eYFP分子的光稳定性提高了6倍,这对闪烁动力学有有益影响。在水溶液中与单链DNA共轭并通过DNA杂交固定在DNA折纸12螺旋束上,使得能够在单分子水平和接近生理条件下对eYFP进行光物理研究。通过对具有160和100 nm设计距离结合位点的12螺旋束DNA折纸纳米尺成像,以及对固定的哺乳动物Vero细胞中的微管成像,证明并定量表征了改善的光物理性质对基于定位的超分辨率显微镜的益处。