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本文引用的文献

1
Side-chain losses in electron capture dissociation to improve peptide identification.电子捕获解离中的侧链损失以改善肽段鉴定
Anal Chem. 2007 Mar 15;79(6):2296-302. doi: 10.1021/ac0619332. Epub 2007 Feb 3.
2
Tandem mass spectrometry of amidated peptides.酰胺化肽段的串联质谱分析
J Mass Spectrom. 2006 Nov;41(11):1470-83. doi: 10.1002/jms.1118.
3
Ion/molecule reactions of cation radicals formed from protonated polypeptides via gas-phase ion/ion electron transfer.通过气相离子/离子电子转移由质子化多肽形成的阳离子自由基的离子/分子反应。
J Am Chem Soc. 2006 Sep 13;128(36):11792-8. doi: 10.1021/ja063248i.
4
Implementation of ion/ion reactions in a quadrupole/time-of-flight tandem mass spectrometer.在四极杆/飞行时间串联质谱仪中实现离子/离子反应
Anal Chem. 2006 Jun 15;78(12):4146-54. doi: 10.1021/ac0606296.
5
Alternately pulsed nanoelectrospray ionization/atmospheric pressure chemical ionization for ion/ion reactions in an electrodynamic ion trap.用于电动离子阱中离子/离子反应的交替脉冲纳米电喷雾电离/大气压化学电离
Anal Chem. 2006 May 1;78(9):3208-12. doi: 10.1021/ac052288m.
6
Long-lived electron capture dissociation product ions experience radical migration via hydrogen abstraction.长寿命电子捕获解离产物离子通过氢提取经历自由基迁移。
J Am Soc Mass Spectrom. 2006 Apr;17(4):576-585. doi: 10.1016/j.jasms.2005.12.015. Epub 2006 Feb 28.
7
Collision-induced dissociation (CID) of peptides and proteins.肽和蛋白质的碰撞诱导解离(CID)
Methods Enzymol. 2005;402:148-85. doi: 10.1016/S0076-6879(05)02005-7.
8
Experimental and theoretical investigations of the loss of amino acid side chains in electron capture dissociation of model peptides.模型肽电子捕获解离过程中氨基酸侧链丢失的实验与理论研究
J Am Soc Mass Spectrom. 2005 Sep;16(9):1523-35. doi: 10.1016/j.jasms.2005.05.001.
9
Complementary structural information from a tryptic N-linked glycopeptide via electron transfer ion/ion reactions and collision-induced dissociation.通过电子转移离子/离子反应和碰撞诱导解离从胰蛋白酶 N 连接糖肽获得的互补结构信息。
J Proteome Res. 2005 Mar-Apr;4(2):628-32. doi: 10.1021/pr049770q.
10
Electron transfer ion/ion reactions in a three-dimensional quadrupole ion trap: reactions of doubly and triply protonated peptides with SO2*-.三维四极杆离子阱中的电子转移离子/离子反应:双质子化和三质子化肽与SO2*-的反应
Anal Chem. 2005 Mar 15;77(6):1831-9. doi: 10.1021/ac0483872.

通过气相离子/离子电子转移解离形成的c和z*离子的离子阱碰撞活化。

Ion trap collisional activation of c and z* ions formed via gas-phase ion/ion electron-transfer dissociation.

作者信息

Han Hongling, Xia Yu, McLuckey Scott A

机构信息

Department of Chemistry, Purdue University, West Lafayette, Indiana 47907-2084, USA.

出版信息

J Proteome Res. 2007 Aug;6(8):3062-9. doi: 10.1021/pr070177t. Epub 2007 Jul 3.

DOI:10.1021/pr070177t
PMID:17608403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2533743/
Abstract

A series of c- and z*-type product ions formed via gas-phase electron-transfer ion/ion reactions between protonated polypeptides with azobenzene radical anions are subjected to ion trap collision activation in a linear ion trap. Fragment ions including a-, b-, y-type and ammonia-loss ions are typically observed in collision induced dissociation (CID) of c ions, showing almost identical CID patterns as those of the C-terminal amidated peptides consisting of the same sequences. Collisional activation of z* species mainly gives rise to side-chain losses and peptide backbone cleavages resulting in a-, b-, c-, x-, y-, and z-type ions. Most of the fragmentation pathways of z* species upon ion trap CID can be accounted for by radical driven processes. The side-chain losses from z* species are different from the small losses observed from the charge-reduced peptide molecular species in electron-transfer dissociation (ETD), which indicates rearrangement of the radical species. Characteristic side-chain losses are observed for several amino acid residues, which are useful to predict their presence in peptide/protein ions. Furthermore, the unique side-chain losses from leucine and isoleucine residues allow facile distinction of these two isomeric residues.

摘要

通过质子化多肽与偶氮苯自由基阴离子之间的气相电子转移离子/离子反应形成的一系列c型和z型产物离子,在线性离子阱中进行离子阱碰撞活化。在c离子的碰撞诱导解离(CID)中通常会观察到包括a型、b型、y型和氨损失离子在内的碎片离子,其CID模式与由相同序列组成的C端酰胺化肽几乎相同。z物种的碰撞活化主要导致侧链损失和肽主链裂解,产生a型、b型、c型、x型、y型和z型离子。离子阱CID作用下z物种的大多数碎片化途径可以用自由基驱动过程来解释。z物种的侧链损失与电子转移解离(ETD)中电荷减少的肽分子物种观察到的小损失不同,这表明自由基物种发生了重排。观察到几个氨基酸残基的特征性侧链损失,这有助于预测它们在肽/蛋白质离子中的存在。此外,亮氨酸和异亮氨酸残基独特的侧链损失使得这两个异构体残基易于区分。