菁
部分
化学
荧光
接受者
费斯特共振能量转移
光化学
罗丹明
罗丹明B
乙二胺
立体化学
无机化学
有机化学
催化作用
凝聚态物理
物理
光催化
量子力学
作者
Yibin Zhang,Jianheng Bi,Shuai Xia,Wafa Mazi,Shulin Wan,Logan Mikesell,Rudy L. Luck,Haiying Liu
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2018-10-18
卷期号:23 (10): 2679-2679
被引量:26
标识
DOI:10.3390/molecules23102679
摘要
A fluorescence resonance energy transfer (FRET)-based near-infrared fluorescent probe (B+) for double-checked sensitive detection of intracellular pH changes has been synthesized by binding a near-infrared rhodamine donor to a near-infrared cyanine acceptor through robust C-N bonds via a nucleophilic substitution reaction. To demonstrate the double-checked advantages of probe B+, a near-infrared probe (A) was also prepared by modification of a near-infrared rhodamine dye with ethylenediamine to produce a closed spirolactam residue. Under basic conditions, probe B+ shows only weak fluorescence from the cyanine acceptor while probe A displays nonfluorescence due to retention of the closed spirolactam form of the rhodamine moiety. Upon decrease in solution pH level, probe B+ exhibits a gradual fluorescence increase from rhodamine and cyanine constituents at 623 nm and 743 nm respectively, whereas probe A displays fluorescence increase at 623 nm on the rhodamine moiety as acidic conditions leads to the rupture of the probe spirolactam rings. Probes A and B+ have successfully been used to monitor intracellular pH alternations and possess pKa values of 5.15 and 7.80, respectively.
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