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w-Type ions formed by electron transfer dissociation of Cys-containing peptides investigated by infrared ion spectroscopy

机译:通过电子传递解离通过红外离子光谱研究的含Cys的肽的电子转移离解形成的W型离子

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摘要

In mass spectrometry-based peptide sequencing, electron transfer dissociation (ETD) and electron capture dissociation (ECD) have become well-established fragmentation methods complementary to collision-induced dissociation. The dominant fragmentation pathways during ETD and ECD primarily involve the formation of c- and z(center dot)-type ions by cleavage of the peptide backbone at the NC bond, although neutral losses from amino acid side chains have also been observed. Residue-specific neutral side chain losses provide useful information when conducting database searching and de novo sequencing. Here, we use a combination of infrared ion spectroscopy and quantum-chemical calculations to assign the structures of two ETD-generated w-type fragment ions. These ions are spontaneously formed from ETD-generated z(center dot)-type fragments by neutral loss of 33Da in peptides containing a cysteine residue. Analysis of the infrared ion spectra confirms that these z(center dot)-ions expel a thiol radical (SH center dot) and that a vinyl CC group is formed at the cleavage site. z(center dot)-type fragments containing a Cys residue but not at the cleavage site do not spontaneously expel a thiol radical, but only upon additional collisional activation after ETD.
机译:在基于质谱的肽测序中,电子转移解离(ETD)和电子捕获解离(ECD)已成为与碰撞诱导的解离的良好成熟的碎片方法。 ETD和ECD期间的显性碎片途径主要涉及通过在NC键处切割肽骨架而形成C-和Z(中心点)型离子,但也观察到来自氨基酸侧链的中性损失。在进行数据库搜索和DE Novo测序时,残留物特异性中性侧链损耗提供了有用的信息。这里,我们使用红外离子光谱和量子化学计算的组合来分配两个ETD产生的W型片段离子的结构。这些离子由ETD-生成的Z(中心点)型分段自发地由含有半胱氨酸残基的肽中的33da的中性损失形成。对红外离子光谱的分析证实这些Z(中心点) - 酮驱逐硫醇基质(SH中心点),并且在切割位点处形成乙烯基Cc基团。 Z(中心点)型含有Cys残留物但不在切割位点的型片段不会自发地驱逐硫醇自由基,而是仅在ETD之后额外的碰撞激活。

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