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Atmospheric pressure neutral reionization mass spectrometry for structural analysis

机译:大气压中性电离质谱用于结构分析

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摘要

Ion dissociation is the usual basis for tandem MS analysis but a significant limitation is that only charged fragments from ion dissociation events are detected while neutral fragments are simply lost. This study reports our continued effort to solve this problem by developing atmospheric pressure neutral reionization mass spectrometry (APNR). In APNR, analyte ions are thermally dissociated (atmospheric pressure thermal dissociation, APTD) followed by soft reionization using electrosonic spray ionization (ESSI). Our results show that APNR is a powerful method for structural analysis of various biomolecules such as peptides, saccharides and nucleotides, as well as for elucidating unimolecular ion dissociation mechanisms. It was found that APNR provides extensive fragment ions including a series of y ions in peptides, which benefit sequencing and provide complementary information to collision induced dissociation (CID). In particular, direct cleavage of disulfide bonds of peptides occurs during APTD, facilitating peptide sequencing and disulfide bond mapping. In addition, many cross-ring cleavage fragments are detected during APNR analysis of oligosaccharides, indicating that the APTD dissociation process is energetic and potentially useful for identifying glycan linkage sites. Fragmentation patterns of oligosaccharide isomers can be used for their differentiation. Furthermore, in the cases of dissociation of nucleotides and synthetic naphthoylindole drugs, the putative neutral, phosphorylated riboses and indoles, were successfully detected using APNR, providing strong evidence to confirm previously proposed unimolecular ion dissociation mechanisms. We believe this APNR technique along with APTD should be of high value in structure determination of biomolecules.
机译:离子解离是串联质谱分析的常规基础,但是一个重要的局限性是仅检测到来自离子解离事件的带电碎片,而中性碎片则丢失了。这项研究报告了我们通过开发大气压中性电离质谱法(APNR)来解决这一问题的持续努力。在APNR中,对分析物离子进行热离解(大气压热离解,APTD),然后使用超声波喷雾电离(ESSI)进行软离化。我们的结果表明,APNR是一种强大的方法,可用于各种生物分子的结构分析,例如肽,糖和核苷酸,以及阐明单分子离子解离机理。发现APNR提供了广泛的片段离子,包括肽中的一系列y离子,这有利于测序并为碰撞诱导解离(CID)提供补充信息。特别地,在APTD期间发生了肽的二硫键的直接裂解,从而促进了肽测序和二硫键作图。另外,在寡糖的APNR分析过程中检测到许多交叉环切割片段,表明APTD的解离过程是有活力的,对于识别聚糖连接位点可能很有用。寡糖异构体的片段化模式可用于其分化。此外,在核苷酸解离和合成萘吲哚类药物解离的情况下,使用APNR成功检测到推定的中性,磷酸化核糖和吲哚,为证实先前提出的单分子离子解离机制提供了有力证据。我们认为,APNR技术与APTD技术一起在生物分子的结构确定中应具有很高的价值。

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