Department of Chemistry and Skaggs Institute for Chemical Biology, the Scripps Research Institute , 10550 N Torrey Pines Road, La Jolla, California 92037, United States.
J Am Chem Soc. 2017 Sep 13;139(36):12350-12353. doi: 10.1021/jacs.7b05725. Epub 2017 Aug 31.
Sirtuins are NAD dependent protein deacetylases, which are involved in many biological processes. We now report a novel genetically encoded fluorescent probe (EGFP-K85AcK) that responds to sirtuins in living cells. The probe design exploits a lysyl residue in EGFP that is essential for chromophore maturation, and is also an efficient deacetylation substrate for sirtuins. Analysis of activity in Escherichia coli ΔcobB revealed that the probe can respond to various human sirtuins, including SIRT1, SIRT2, SIRT3 and SIRT5. We also directly monitored SIRT1 and SIRT2 activity in HEK293T cells with an mCherry fusion of EGFP-K85AcK, and showed that this approach can be extended to other fluorescent proteins. Finally, we demonstrate that this approach can be used to examine the activity of sirtuins toward additional lysyl posttranslational modifications, and show that sirtuins can act as erasers of HibK modified proteins.
Sirtuins 是依赖 NAD 的蛋白去乙酰化酶,参与许多生物学过程。我们现在报告一种新型的遗传编码荧光探针(EGFP-K85AcK),它可以在活细胞中响应 sirtuins。该探针的设计利用了 EGFP 中的一个赖氨酸残基,该残基对于生色团成熟至关重要,也是 sirtuins 的有效去乙酰化底物。在大肠杆菌 ΔcobB 中的活性分析表明,该探针可以响应各种人类 sirtuins,包括 SIRT1、SIRT2、SIRT3 和 SIRT5。我们还通过 EGFP-K85AcK 的 mCherry 融合直接监测了 HEK293T 细胞中的 SIRT1 和 SIRT2 活性,并表明这种方法可以扩展到其他荧光蛋白。最后,我们证明这种方法可以用于研究 sirtuins 对其他赖氨酸翻译后修饰的活性,并表明 sirtuins 可以作为 HibK 修饰蛋白的橡皮擦。