Tran Jeremy C, Kuffner Christopher J, Marzilli Alexander M, Miller Ryan Emily, Silfen Zachary E, McMahan Jeffrey B, Sloas D Christopher, Chen Christopher S, Ngo John T
bioRxiv. 2024 Jun 12:2024.06.12.598538. doi: 10.1101/2024.06.12.598538.
We introduce an adaptor-based strategy for regulating fluorescein-binding synthetic Notch (SynNotch) receptors using ligands based on conjugates of fluorescein isomers and analogs. To develop a versatile system, we evaluated the surface expression and activities of multiple constructs containing distinct extracellular fluorescein-binding domains. Using an optimized receptor, we devised ways to regulate signaling via fluorescein-based chemical transformations, including an approach based on a bio-orthogonal chemical ligation and a spatially controllable strategy via the photo-patterned uncaging of an -nitrobenzyl-caged fluorescein conjugate. We further demonstrate that fluorescein-conjugated extracellular matrix (ECM)-binding peptides can regulate SynNotch activity depending on the folding state of collagen-based ECM networks. Treatment with these conjugates enabled cells to distinguish between folded versus denatured collagen proteins and enact dose-dependent gene expression responses depending on the nature of the signaling adaptors presented. To demonstrate the utility of these tools, we applied them to control the myogenic conversion of fibroblasts into myocytes with spatial and temporal precision and in response to denatured collagen-I, a biomarker of multiple pathological states. Overall, we introduce an optimized fluorescein-binding SynNotch as a versatile tool for regulating transcriptional responses to extracellular ligands based on the widely used and clinically-approved fluorescein dye.
我们介绍了一种基于衔接子的策略,用于使用基于荧光素异构体和类似物共轭物的配体来调节荧光素结合型合成Notch(SynNotch)受体。为了开发一个通用系统,我们评估了多个含有不同细胞外荧光素结合结构域的构建体的表面表达和活性。使用优化后的受体,我们设计了通过基于荧光素的化学转化来调节信号传导的方法,包括一种基于生物正交化学连接的方法和一种通过光图案化释放α-硝基苄基笼蔽的荧光素共轭物实现的空间可控策略。我们进一步证明,荧光素共轭的细胞外基质(ECM)结合肽可以根据基于胶原蛋白的ECM网络的折叠状态来调节SynNotch活性。用这些共轭物处理使细胞能够区分折叠型与变性的胶原蛋白,并根据所呈现的信号衔接子的性质产生剂量依赖性基因表达反应。为了证明这些工具的实用性,我们将它们应用于以空间和时间精度控制成纤维细胞向肌细胞的肌源性转化,并响应变性的I型胶原蛋白(多种病理状态的生物标志物)。总体而言,我们引入了一种优化的荧光素结合型SynNotch,作为一种通用工具,用于基于广泛使用且经临床批准的荧光素染料来调节对细胞外配体的转录反应。