Fiore Antonio, Yu Guoqiang, Northey Jason J, Patel Ronak, Ravenscroft Thomas A, Ikegami Richard, Kolkman Wiert, Kumar Pratik, Grimm Jonathan B, Dilan Tanya L, Ruetten Virginia M S, Ahrens Misha B, Shroff Hari, Lavis Luke D, Wang Shaohe, Weaver Valerie M, Pedram Kayvon
Janelia Research Campus, Howard Hughes Medical Institute (HHMI), Ashburn, VA, USA.
Center for Bioengineering and Tissue Regeneration, Department of Surgery, University of California, San Francisco (UCSF), San Francisco, CA, USA.
bioRxiv. 2024 May 10:2024.05.09.593460. doi: 10.1101/2024.05.09.593460.
All multicellular systems produce and dynamically regulate extracellular matrices (ECM) that play important roles in both biochemical and mechanical signaling. Though the spatial arrangement of these extracellular assemblies is critical to their biological functions, visualization of ECM structure is challenging, in part because the biomolecules that compose the ECM are difficult to fluorescently label individually and collectively. Here, we present a cell-impermeable small molecule fluorophore, termed Rhobo6, that turns on and red shifts upon reversible binding to glycans. Given that most ECM components are densely glycosylated, the dye enables wash-free visualization of ECM, in systems ranging from substrates to mouse mammary tumors. Relative to existing techniques, Rhobo6 provides a broad substrate profile, superior tissue penetration, nonperturbative labeling, and negligible photobleaching. This work establishes a straightforward method for imaging the distribution of ECM in live tissues and organisms, lowering barriers for investigation of extracellular biology.
所有多细胞系统都会产生并动态调节细胞外基质(ECM),其在生化信号和机械信号传导中均发挥着重要作用。尽管这些细胞外组件的空间排列对其生物学功能至关重要,但ECM结构的可视化颇具挑战,部分原因在于构成ECM的生物分子难以单独或集体进行荧光标记。在此,我们展示了一种细胞不可渗透的小分子荧光团,称为Rhobo6,它在与聚糖可逆结合时开启并发生红移。鉴于大多数ECM成分都高度糖基化,该染料能够在从底物到小鼠乳腺肿瘤等多种系统中实现无需冲洗的ECM可视化。相对于现有技术,Rhobo6具有广泛的底物谱、出色的组织穿透性、非干扰性标记以及可忽略不计的光漂白现象。这项工作建立了一种直接的方法来成像活组织和生物体中ECM的分布,降低了细胞外生物学研究的障碍。