用于电化学生物传感应用的无金属邻苯二胺标记肽核酸

IF 2.9 Q2 ELECTROCHEMISTRY Electrochemical science advances Pub Date : 2022-02-06 DOI:10.1002/elsa.202100164
Mirko Magni, Sergio Dall'Angelo, Clara Baldoli, Emanuela Licandro, Luigi Falciola, Patrizia R. Mussini
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引用次数: 1

摘要

肽核酸(PNAs)是天然DNA和RNA生物聚合物的中性模拟物,已经引起了从事DNA/RNA链中特定核碱基序列鉴定的研究人员的注意。为此,需要开发特定的分析方案来优化PNAs的核酸识别能力,利用PNA/DNA(RNA)偶对的高内在亲和力以及与PNA主干连接或在工作介质中与其适当相互作用的合适标记。在这种情况下,本文报道了邻苯二胺和4-硝基邻苯二胺作为两种廉价的、无金属的电活性标记物,共价结合到PNA十聚体的伪肽主链上。在对标记物和PNA偶联物进行初步表征后,人们的注意力转向了水溶液中标记的PNA十聚体的可检测性的优化。利用悬垂汞滴电极上的电位溶出分析,可以达到约10 nM的令人满意的检测限,避免使用昂贵的过渡金属配合物作为标签和/或共试剂。
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Metal-free phthalimide-labeled peptide nucleic acids for electrochemical biosensing applications

Peptide nucleic acids (PNAs) are neutral mimics of natural DNA and RNA biopolymers that have caught the attention of researchers working on the identification of specific sequences of nucleobases in DNA/RNA strands. For this purpose, specific analytical protocols need to be developed to optimize the nucleic acid recognition ability of PNAs, exploiting both the high intrinsic affinity of PNA/DNA(RNA) couples as well as suitable markers, either linked to the PNA backbone or properly interacting with it in the working medium. In this context, the paper reports on phthalimide and 4-nitrophthalimide as two cheap, metal-free electroactive markers covalently bound to the pseudo-peptide backbone of a PNA decamer. After a preliminary characterization of the markers, as such and in PNA conjugates, attention has been moved toward the optimization of the detectability of the labeled PNA decamers in aqueous solutions. Exploiting the potentiometric stripping analysis on hanging mercury drop electrode it has been possible to reach satisfactory detection limits of ca. 10 nM avoiding the use of expensive transition metal complexes as labels and/or of co-reagents.

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CiteScore
3.80
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审稿时长
10 weeks
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