Bioengineering, Stanford University, Stanford, CA, USA.
BioX Institute, Stanford University, Stanford, CA, USA.
Nat Chem Biol. 2019 Apr;15(4):401-409. doi: 10.1038/s41589-019-0241-6. Epub 2019 Mar 11.
We describe three optical tags, ArrayG, ArrayD and ArrayG/N, for intracellular tracking of single molecules over milliseconds to hours. ArrayG is a fluorogenic tag composed of a green fluorescent protein-nanobody array and monomeric wild-type green fluorescent protein binders that are initially dim but brighten ~26-fold on binding with the array. By balancing the rates of binder production, photobleaching and stochastic binder exchange, we achieve temporally unlimited tracking of single molecules. High-speed tracking of ArrayG-tagged kinesins and integrins for thousands of frames reveals novel dynamical features. Tracking of single histones at 0.5 Hz for >1 hour with the import competent ArrayG/N tag shows that chromosomal loci behave as Rouse polymers with visco-elastic memory and exhibit a non-Gaussian displacement distribution. ArrayD, based on a dihydrofolate reductase nanobody array and dihydrofolate reductase-fluorophore binder, enables dual-color imaging. The arrays combine brightness, fluorogenicity, fluorescence replenishment and extended fluorophore choice, opening new avenues for tracking single molecules in living cells.
我们描述了三种光学标签,ArrayG、ArrayD 和 ArrayG/N,用于在毫秒到小时的时间范围内对单个分子进行细胞内跟踪。ArrayG 是一种由绿色荧光蛋白-纳米体阵列和单体野生型绿色荧光蛋白结合物组成的荧光标签,在与阵列结合时最初是暗的,但会增亮约 26 倍。通过平衡结合物产生、光漂白和随机结合物交换的速率,我们实现了对单个分子的时间上无限制的跟踪。用 ArrayG 标记的驱动蛋白和整合素进行数千帧的高速跟踪揭示了新的动态特征。用具有导入能力的 ArrayG/N 标签以 0.5 Hz 的速度跟踪单个组蛋白超过 1 小时显示,染色体位置表现为具有粘弹性记忆的 Rouse 聚合物,并表现出非高斯位移分布。基于二氢叶酸还原酶纳米体阵列和二氢叶酸还原酶-荧光团结合物的 ArrayD 能够进行双色成像。这些阵列结合了亮度、荧光性、荧光补充和扩展的荧光团选择,为在活细胞中跟踪单个分子开辟了新途径。