Department of Chemistry, University of California, Irvine, 1120 Natural Science II, Irvine, CA, 92697, USA.
Department of Molecular Biology and Biochemistry, University of California, Irvine, 3205 McGaugh Hall, Irvine, CA, 92697, USA.
Chembiochem. 2021 Aug 17;22(16):2650-2654. doi: 10.1002/cbic.202100202. Epub 2021 Jun 30.
Bioluminescent tools have been used for decades to image processes in complex tissues and preclinical models. However, few distinct probes are available to probe multicellular interactions. We and others are addressing this limitation by engineering new luciferases that can selectively process synthetic luciferin analogues. In this work, we explored naphthylamino luciferins as orthogonal bioluminescent probes. Three analogues were prepared using an optimized synthetic route. The luciferins were found to be robust emitters with native luciferase in vitro and in cellulo. We further screened the analogues against libraries of luciferase mutants to identify unique enzyme-substrate pairs. The new probes can be used in conjunction with existing bioluminescent tools for multi-component imaging.
生物发光工具已被用于对复杂组织和临床前模型中的过程进行成像数十年。然而,能够探测细胞间相互作用的独特探针却寥寥无几。我们和其他人正在通过设计能够选择性地处理合成荧光素类似物的新荧光素酶来解决这一限制。在这项工作中,我们探索了萘氨基荧光素作为正交生物发光探针。使用优化的合成路线制备了三种类似物。在体外和细胞内,发现这些荧光素与天然荧光素一样是强大的发射器。我们进一步对文库中的荧光素酶突变体进行筛选,以鉴定独特的酶-底物对。这些新探针可以与现有的生物发光工具一起用于多组分成像。