萤光素酶类
生物发光
生物发光成像
荧光素酶
荧光素
化学
基质(水族馆)
计算生物学
生物化学
底物特异性
酶
生物系统
生物物理学
纳米技术
生物
基因
材料科学
转染
生态学
作者
Krysten A. Jones,William B. Porterfield,Colin M. Rathbun,David M. McCutcheon,Miranda A. Paley,Jennifer A. Prescher
摘要
Bioluminescence imaging with luciferase-luciferin pairs is widely used in biomedical research. Several luciferases have been identified in nature, and many have been adapted for tracking cells in whole animals. Unfortunately, the optimal luciferases for imaging in vivo utilize the same substrate and therefore cannot easily differentiate multiple cell types in a single subject. To develop a broader set of distinguishable probes, we crafted custom luciferins that can be selectively processed by engineered luciferases. Libraries of mutant enzymes were iteratively screened with sterically modified luciferins, and orthogonal enzyme-substrate "hits" were identified. These tools produced light when complementary enzyme-substrate partners interacted both in vitro and in cultured cell models. Based on their selectivity, these designer pairs will bolster multicomponent imaging and enable the direct interrogation of cell networks not currently possible with existing tools. Our screening platform is also general and will expedite the identification of more unique luciferases and luciferins, further expanding the bioluminescence toolkit.
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