Imaging the extracellular matrix in live tissues and organisms with a glycan-binding fluorophore

Author:

Fiore AntonioORCID,Yu Guoqiang,Northey Jason J.ORCID,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.ORCID,Wang Shaohe,Weaver Valerie M.,Pedram KayvonORCID

Abstract

AbstractAll 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 fromin vitrosubstrates toin vivomouse 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.

Publisher

Cold Spring Harbor Laboratory

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