• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

目标物身份和碰撞能量对一些质量选择的质子化神经肽碎片化的影响。

Effects of target identity and collision energy on the fragmentation of some mass-selected protonated neuropeptides.

作者信息

Curcuruto O, Hamdan M

机构信息

Glaxo Research Laboratories, Verona, Italy.

出版信息

Rapid Commun Mass Spectrom. 1993 Nov;7(11):989-93. doi: 10.1002/rcm.1290071105.

DOI:10.1002/rcm.1290071105
PMID:7904194
Abstract

A number of protonated neuropetides formed by 10 keV Cs+ ion bombardment are mass selected and their collision-induced dissociations (CID) with helium, argon, xenon and isobutane are monitored using a collision energy of 200 eV. Data obtained by fixing the collision gas and using translational energies in the range 50-250 eV are also presented. The present data imply that optimization of the CID spectra presented can be achieved through a judicious choice of both the target gas and the translational energy of the mass-selected ion. The combined effect of the two experimental parameters on the relative abundances of the major sequence ions and on the loss of side-chain moieties is discussed.

摘要

通过10 keV Cs⁺离子轰击形成的多种质子化神经肽被进行质量选择,并使用200 eV的碰撞能量监测它们与氦气、氩气、氙气和异丁烷的碰撞诱导解离(CID)。还展示了通过固定碰撞气体并使用50 - 250 eV范围内的平动能所获得的数据。目前的数据表明,通过明智地选择目标气体和质量选择离子的平动能,可以实现所呈现的CID光谱的优化。讨论了这两个实验参数对主要序列离子的相对丰度以及侧链部分损失的综合影响。

相似文献

1
Effects of target identity and collision energy on the fragmentation of some mass-selected protonated neuropeptides.目标物身份和碰撞能量对一些质量选择的质子化神经肽碎片化的影响。
Rapid Commun Mass Spectrom. 1993 Nov;7(11):989-93. doi: 10.1002/rcm.1290071105.
2
Effect of different target gases on low-energy collision-activated dissociation of peptides.不同目标气体对肽段低能碰撞激活解离的影响。
Rapid Commun Mass Spectrom. 1990 Jul;4(7):251-5. doi: 10.1002/rcm.1290040706.
3
Ion trap versus low-energy beam-type collision-induced dissociation of protonated ubiquitin ions.离子阱与质子化泛素离子的低能束型碰撞诱导解离
Anal Chem. 2006 Feb 15;78(4):1218-27. doi: 10.1021/ac051622b.
4
Fragmentation characteristics of neuropeptides related to chromogranin B and proenkephalin B using fast atom bombardment and collision-induced dissociation.
Biol Mass Spectrom. 1994 Oct;23(10):603-11. doi: 10.1002/bms.1200231002.
5
Collision-induced dissociation of some protonated peptides with and without mass selection.有质量选择和无质量选择情况下一些质子化肽的碰撞诱导解离。
Rapid Commun Mass Spectrom. 1994 Mar;8(3):274-9. doi: 10.1002/rcm.1290080310.
6
Ion activation methods for tandem mass spectrometry.串联质谱的离子激活方法。
J Mass Spectrom. 2004 Oct;39(10):1091-112. doi: 10.1002/jms.703.
7
Fragmentation reactions of protonated peptides containing glutamine or glutamic acid.含有谷氨酰胺或谷氨酸的质子化肽的碎片化反应。
J Mass Spectrom. 2003 Feb;38(2):174-87. doi: 10.1002/jms.427.
8
Optimization of matrix-assisted laser desorption/ionization time-of-flight collision-induced dissociation using poly(ethylene glycol).使用聚乙二醇优化基质辅助激光解吸/电离飞行时间碰撞诱导解离
Rapid Commun Mass Spectrom. 2003;17(14):1671-6. doi: 10.1002/rcm.1084.
9
Multi-stage tandem mass spectrometry of metal cationized leucine enkephalin and leucine enkephalin amide.金属阳离子化亮氨酸脑啡肽和亮氨酸脑啡肽酰胺的多级串联质谱分析
Rapid Commun Mass Spectrom. 2002;16(6):566-78. doi: 10.1002/rcm.612.
10
Fragmentation of a series of cyclic dipeptides in fast-atom bombardment mass spectrometry.快速原子轰击质谱法中一系列环二肽的碎片化
Rapid Commun Mass Spectrom. 1995;9(9):800-3. doi: 10.1002/rcm.1290090917.

引用本文的文献

1
Radical difluoromethylthiolation of aromatics enabled by visible light.可见光介导的芳烃的自由基二氟甲硫基化反应
Chem Sci. 2018 Jun 1;9(26):5781-5786. doi: 10.1039/c8sc01669k. eCollection 2018 Jul 14.
2
Collision induced decomposition of peptides. Choice of collision parameters.肽的碰撞诱导分解。碰撞参数的选择。
J Am Soc Mass Spectrom. 1996 Jul;7(7):677-81. doi: 10.1016/1044-0305(96)85613-3.