脱氧核酶
荧光
化学
绿色荧光蛋白
水溶液中的金属离子
费斯特共振能量转移
金属
生物传感器
流式细胞术
赫拉
荧光蛋白
生物物理学
纳米技术
DNA
分子生物学
材料科学
生物化学
生物
细胞
基因
有机化学
物理
量子力学
作者
Mengyi Xiong,Zhenglin Yang,Ryan J. Lake,Junjie Li,Shanni Hong,Huanhuan Fan,Xiaobing Zhang,Yi Lu
标识
DOI:10.1002/anie.201912514
摘要
Abstract Genetically encoded fluorescent proteins (FPs) have been used for metal ion detection. However, their applications are restricted to a limited number of metal ions owing to the lack of available metal‐binding proteins or peptides that can be fused to FPs and the difficulty in transforming the binding of metal ions into a change of fluorescent signal. We report herein the use of Mg 2+ ‐specific 10–23 or Zn 2+ ‐specific 8–17 RNA‐cleaving DNAzymes to regulate the expression of FPs as a new class of ratiometric fluorescent sensors for metal ions. Specifically, we demonstrate the use of DNAzymes to suppress the expression of Clover2, a variant of the green FP (GFP), by cleaving the mRNA of Clover2, while the expression of Ruby2, a mutant of the red FP (RFP), is not affected. The Mg 2+ or Zn 2+ in HeLa cells can be detected using both confocal imaging and flow cytometry. Since a wide variety of metal‐specific DNAzymes can be obtained, this method can likely be applied to imaging many other metal ions, expanding the range of the current genetically encoded fluorescent protein‐based sensors.
科研通智能强力驱动
Strongly Powered by AbleSci AI