| Literature DB >> 29215269 |
Shui-Ping Yang1, Wei Zhao1, Pei-Pei Hu1, Ke-Yang Wu1, Zhi-Hong Jiang2, Li-Ping Bai2, Min-Min Li3, Jin-Xiang Chen1.
Abstract
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.Entities:
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Year: 2017 PMID: 29215269 DOI: 10.1021/acs.inorgchem.7b02107
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165