一氧化碳
荧光
化学
试剂
斑马鱼
血红素
检出限
金属
红外线的
生物物理学
组合化学
生物化学
酶
催化作用
生物
色谱法
物理化学
有机化学
物理
量子力学
光学
基因
作者
Zuokai Wang,Caiyun Liu,Xin Wang,Qingxia Duan,Pan Jia,Hanchuang Zhu,Zilu Li,Xue Zhang,Xiaohua Ren,Baocun Zhu,Wenlong Sheng
标识
DOI:10.1016/j.snb.2019.04.084
摘要
In this work, by taking full advantage of the transformation of nitro group into amino moiety under the direct reduction of CO, a new metal-free colorimetric and near-infrared fluorescent probe NIR-CO for rapid and specific tracing of intracellular CO has been constructed, and it also become the first reaction-based near-infrared fluorescent probe for CO detection without additional reagents. Probe NIR-CO could quantitatively detect CO at the nanomolar level and the detection limit was calculated as low as 6.1 nM. Additionally, probe NIR-CO with preeminent sensing properties was successfully applied to monitor the fluctuations of endogenous CO levels in living systems. In particular, the up-regulation of heme oxygenase-1 (HO-1) caused by transient glucose deprivation (TGD) in living cells and the down-regulation of HO-1 inhibited by high glucose (HG) in zebrafish were confirmed for the first time via mapping the glucose-induced fluctuations of CO levels. Thus, we anticipate that probe NIR-CO not only can serve as a powerful tool to investigate the detailed biological functions of CO in the pathophysiological processes, but also possesses potential applications of in situ monitoring HO-1 activity in the complex biological systems.
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