Program in Chemical Biology, University of Michigan, Ann Arbor, Michigan 48109, United States.
Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.
ACS Chem Biol. 2021 Nov 19;16(11):2109-2115. doi: 10.1021/acschembio.1c00391. Epub 2021 Oct 15.
Bilin-binding fluorescent proteins like UnaG-bilirubin are noncovalent ligand-dependent reporters for oxygen-free microscopy but are restricted to blue and far-red fluorescence. Here we describe a high-throughput screening approach to provide a new UnaG-ligand pair that can be excited in the 532 nm green excitation microscopy channel. We identified a novel orange UnaG-ligand pair that maximally emits at 581 nm. Whereas the benzothiazole-based ligand itself is nominally fluorescent, the compound binds UnaG with high affinity ( = 3 nM) to induce a 2.5-fold fluorescence intensity enhancement and a 10 nm red shift. We demonstrated this pair in the anaerobic fluorescence microscopy of the prevalent gut bacterium and in . This UnaG-ligand pair can also be coupled to IFP2.0-biliverdin to differentiate cells in mixed-species two-color imaging. Our results demonstrate the versatility of the UnaG ligand-binding pocket and extend the ability to image cells at longer wavelengths in anoxic environments.
结合胆红素的双荧光蛋白是非共价配体依赖性的无氧显微镜报告分子,但它们仅限于蓝色和远红色荧光。在这里,我们描述了一种高通量筛选方法,以提供一种新的可在 532nm 绿色激发显微镜通道中激发的 UnaG-配体对。我们鉴定出一种新的橙色 UnaG-配体对,其最大发射波长为 581nm。虽然基于苯并噻唑的配体本身具有荧光性,但该化合物与 UnaG 具有高亲和力(=3nM),可诱导荧光强度增强 2.5 倍和红移 10nm。我们在常见肠道细菌的厌氧荧光显微镜中以及 中证明了这一对。该 UnaG-配体对也可以与 IFP2.0-胆红素结合,以区分混合物种双色成像中的细胞。我们的结果证明了 UnaG 配体结合口袋的多功能性,并扩展了在缺氧环境中以更长波长对细胞进行成像的能力。