Jradi Fadi M, English Brian P, Brown Timothy A, Aaron Jesse, Khuon Satya, Galbraith James A, Galbraith Catherine G, Lavis Luke D
Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, 20147, USA.
Department of Biomedical Engineering and Knight Cancer Institute, Oregon Health and Science University, Portland, OR, USA.
bioRxiv. 2024 May 12:2024.05.12.593749. doi: 10.1101/2024.05.12.593749.
Single-molecule localization microscopy (SMLM) uses activatable or switchable fluorophores to create non-diffraction limited maps of molecular location in biological samples. Despite the utility of this imaging technique, the portfolio of appropriate labels for SMLM remains limited. Here, we describe a general strategy for the construction of "glitter bomb" labels by simply combining rhodamine and coumarin dyes though an amide bond. Condensation of the -carboxyl group on the pendant phenyl ring of rhodamine dyes with a 7-aminocoumarin yields photochromic or spontaneously blinking fluorophores depending on the parent rhodamine structure. We apply this strategy to prepare labels useful super-resolution experiments in fixed cells using different attachment techniques. This general glitter bomb strategy should lead to improved labels for SMLM, ultimately enabling the creation of detailed molecular maps in biological samples.
单分子定位显微镜(SMLM)使用可激活或可切换的荧光团来创建生物样品中分子位置的非衍射极限图谱。尽管这种成像技术很有用,但适用于SMLM的标记物种类仍然有限。在这里,我们描述了一种通过酰胺键简单地将罗丹明和香豆素染料结合来构建“闪光弹”标记物的通用策略。罗丹明染料侧链苯环上的羧基与7-氨基香豆素缩合,根据母体罗丹明结构产生光致变色或自发闪烁的荧光团。我们应用这一策略,通过不同的连接技术制备了适用于固定细胞超分辨率实验的标记物。这种通用的闪光弹策略应该会产生改进的SMLM标记物,最终能够在生物样品中创建详细的分子图谱。