化学
核糖核酸
羧酸盐
选择性
溴化物
DNA
荧光
金属有机骨架
组合化学
立体化学
无机化学
生物化学
基因
有机化学
催化作用
吸附
物理
量子力学
作者
Shuiping Yang,Wei Zhao,Peipei Hu,Ke-Yang Wu,Zhi‐Hong Jiang,Li‐Ping Bai,Minmin Li,Jin-Xiang Chen
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2017-12-07
卷期号:56 (24): 14880-14887
被引量:51
标识
DOI:10.1021/acs.inorgchem.7b02107
摘要
Reactions of La(NO3)3·6H2O with the polar, tritopic quaternized carboxylate ligands N-carboxymethyl-3,5-dicarboxylpyridinium bromide (H3CmdcpBr) and N-(4-carboxybenzyl)-3,5-dicarboxylpyridinium bromide (H3CbdcpBr) afford two water-stable metal–organic frameworks (MOFs) of {[La4(Cmdcp)6(H2O)9]}n (1, 3D) and {[La2(Cbdcp)3(H2O)10]}n (2, 2D). MOFs 1 and 2 absorb the carboxyfluorescein (FAM)-tagged probe DNA (P-DNA) and quench the fluorescence of FAM via a photoinduced electron transfer (PET) process. The nonemissive P-DNA@MOF hybrids thus formed in turn function as sensing platforms to distinguish conservative linear, single-stranded RNA sequences of Sudan virus with high selectivity and low detection limits of 112 and 67 pM, respectively (at a signal-to-noise ratio of 3). These hybrids also exhibit high specificity and discriminate down to single-base mismatch RNA sequences.
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