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Electrospray ionisation-cleavable tandem nucleic acid mass tag–peptide nucleic acid conjugates: synthesis and applications to quantitative genomic analysis using electrospray ionisation-MS/MS

机译:电喷雾电离可裂解的串联核酸质量标签-肽核酸共轭物:使用电喷雾电离-MS / MS的合成及其在定量基因组分析中的应用

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摘要

The synthesis and characterization of isotopomer tandem nucleic acid mass tag–peptide nucleic acid (TNT–PNA) conjugates is described along with their use as electrospray ionisation-cleavable (ESI-Cleavable) hybridization probes for the detection and quantification of target DNA sequences by electrospray ionisation tandem mass spectrometry (ESI-MS/MS). ESI-cleavable peptide TNT isotopomers were introduced into PNA oligonucleotide sequences in a total synthesis approach. These conjugates were evaluated as hybridization probes for the detection and quantification of immobilized synthetic target DNAs using ESI-MS/MS. In these experiments, the PNA portion of the conjugate acts as a hybridization probe, whereas the peptide TNT is released in a collision-based process during the ionization of the probe conjugate in the electrospray ion source. The cleaved TNT acts as a uniquely resolvable marker to identify and quantify a unique target DNA sequence. The method should be applicable to a wide variety of assays requiring highly multiplexed, quantitative DNA/RNA analysis, including gene expression monitoring, genetic profiling and the detection of pathogens.
机译:介绍了同位素异构体串联核酸质量标签-肽核酸(TNT-PNA)缀合物的合成和表征,以及它们作为电喷雾电离可裂解(ESI-Cleavable)杂交探针的用途,用于通过电喷雾检测和定量目标DNA序列电离串联质谱(ESI-MS / MS)。将ESI可裂解的肽TNT异构体以全合成方法引入PNA寡核苷酸序列中。这些缀合物被评估为杂交探针,用于使用ESI-MS / MS对固定的合成靶DNA进行检测和定量。在这些实验中,缀合物的PNA部分用作杂交探针,而在电喷雾离子源中探针缀合物的电离过程中,肽TNT在基于碰撞的过程中释放。裂解的TNT充当唯一可分辨的标记,以鉴定和定量唯一的靶DNA序列。该方法应适用于需要高度多重,定量DNA / RNA分析的多种测定,包括基因表达监测,基因谱分析和病原体检测。

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