Sequential Ag+/biothiol and synchronous Ag+/Hg2+ biosensing with zwitterionic Cu2+-based metal-organic frameworks

被引:21
|
作者
Huang, Nai-Han [1 ]
Liu, Yan [2 ]
Li, Rong-Tian [1 ]
Chen, Jing [2 ]
Hu, Pei-Pei [1 ]
Young, David J. [3 ]
Chen, Jin-Xiang [1 ]
Zhang, Wen-Hua [2 ]
机构
[1] Southern Med Univ, Guangdong Prov Key Lab New Drug Screening, Sch Pharmaceut Sci, Guangzhou 510515, Peoples R China
[2] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
[3] Charles Darwin Univ, Coll Engn Informat Technol & Environm, Darwin, NT 0909, Australia
基金
中国国家自然科学基金;
关键词
THYMINE BASE-PAIRS; DRUG-DELIVERY; HG-II; ROOM-TEMPERATURE; CARBON-DIOXIDE; DNA; SEPARATION; CONSTRUCTION; POLYMER; PLATFORM;
D O I
10.1039/d0an00002g
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Zwitterionic metal-organic frameworks (MOFs) of {[Cu(Cbdcp)(Dps)(H2O)(3)]center dot 6H(2)O}(n) (MOF 1) and [Cu-4(Dcbb)(4)(Dps)(2)(H2O)(2)](n) (MOF 2) (H(3)CbdcpBr = N-(4-carboxybenzyl)-(3,5-dicarboxyl)pyridinium bromide; H(2)DcbbBr = 1-(3,5-dicarboxybenzyl)-4,4 '-bipyridinium bromide; Dps = 4,4 '-dipyridyl sulfide) quench the fluorescence of cytosine-rich DNA tagged with 5-carboxytetramethylrhodamine (TAMRA, emission at 582 nm, denoted as C-rich P-DNA-1) and yield the corresponding P-DNA-1@MOF hybrids. Exposure of these hybrids to Ag+ results in the release of the P-DNA-1 strands from the MOF surfaces as double-stranded, hairpin-like C-Ag-I-C (ds-DNA-1@Ag+) with the restoration of TAMRA fluorescence. The ds-DNA-1@Ag+ formed on the surface of 1 can subsequently sense biothiols cysteine (Cys), glutathione (GSH), and homocysteine (Hcy) due to the stronger affinity of mercapto groups for Ag+ that serves to unfold the ds-DNA-1@Ag+ duplex, reforming P-DNA-1, which is re-adsorbed by MOF 1 accompanied by quenching of TAMRA emission. Meanwhile, MOF 2 is also capable of co-loading a thymine-rich probe DNA tagged with 5-carboxyfluorescein (FAM, emission at 518 nm, denoted as T-rich P-DNA-2) to achieve synchronous sensing of Ag+ and Hg2+, resulting from the simultaneous yet specific ds-DNA-1@Ag+ and T-Hg-II-T duplex (ds-DNA-2@Hg2+) formation, as well as the distinctive emission wavelengths of TAMRA and FAM. Detection limits are as low as 5.3 nM (Ag+), 14.2 nM (Cys), 13.5 nM (GSH), and 9.1 nM (Hcy) for MOF 1, and 7.5 nM (Ag+) and 2.6 nM (Hg2+) for MOF 2, respectively. The sequential sensing of Ag+ and biothiols by MOF 1, and the synchronous sensing of Ag+ and Hg2+ by MOF 2 are rapid and specific, even in the presence of other mono- and divalent metal cations or other biothiols at much higher concentrations. Molecular simulation studies provide insights regarding the molecular interactions that underpin these sensing processes.
引用
收藏
页码:2779 / 2788
页数:10
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