Grimm Jonathan B, Brown Timothy A, English Brian P, Lionnet Timothée, Lavis Luke D
Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA.
Methods Mol Biol. 2017;1663:179-188. doi: 10.1007/978-1-4939-7265-4_15.
The development of genetically encoded self-labeling protein tags such as the HaloTag and SNAP-tag has expanded the utility of chemical dyes in microscopy. Intracellular labeling using these systems requires small, cell-permeable dyes with high brightness and photostability. We recently discovered a general method to improve the properties of classic fluorophores by replacing N,N-dimethylamino groups with four-membered azetidine rings to create the "Janelia Fluor" dyes. Here, we describe the synthesis of the HaloTag and SNAP-tag ligands of Janelia Fluor 549 and Janelia Fluor 646 as well as standard labeling protocols for use in ensemble and single-molecule cellular imaging.
诸如HaloTag和SNAP-tag等基因编码的自标记蛋白标签的发展,扩展了化学染料在显微镜技术中的应用。使用这些系统进行细胞内标记需要具有高亮度和光稳定性的小分子、细胞可渗透染料。我们最近发现了一种通用方法,通过用四元氮杂环丁烷环取代N,N-二甲基氨基来改善经典荧光团的性质,从而创建了“Janelia Fluor”染料。在此,我们描述了Janelia Fluor 549和Janelia Fluor 646的HaloTag和SNAP-tag配体的合成,以及用于整体和单分子细胞成像的标准标记方案。