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使用大型簇离子源通过飞行时间二次离子质谱法进行肽片段化和表面结构分析。

Peptide Fragmentation and Surface Structural Analysis by Means of ToF-SIMS Using Large Cluster Ion Sources.

作者信息

Yokoyama Yuta, Aoyagi Satoka, Fujii Makiko, Matsuo Jiro, Fletcher John S, Lockyer Nicholas P, Vickerman John C, Passarelli Melissa K, Havelund Rasmus, Seah Martin P

机构信息

Department of Materials and Life Science, Seikei University , Tokyo 180-8633, Japan.

Quantum Science and Engineering Center, Kyoto University , Kyoto 611-0011, Japan.

出版信息

Anal Chem. 2016 Apr 5;88(7):3592-7. doi: 10.1021/acs.analchem.5b04133. Epub 2016 Mar 9.

Abstract

Peptide or protein structural analysis is crucial for the evaluation of biochips and biodevices, therefore an analytical technique with the ability to detect and identify protein and peptide species directly from surfaces with high lateral resolution is required. In this report, the efficacy of ToF-SIMS to analyze and identify proteins directly from surfaces is evaluated. Although the physics governing the SIMS bombardment process precludes the ability for researchers to detect intact protein or larger peptides of greater than a few thousand mass unit directly, it is possible to obtain information on the partial structures of peptides or proteins using low energy per atom argon cluster ion beams. Large cluster ion beams, such as Ar clusters and C60 ion beams, produce spectra similar to those generated by tandem MS. The SIMS bombardment process also produces peptide fragment ions not detected by conventional MS/MS techniques. In order to clarify appropriate measurement conditions for peptide structural analysis, peptide fragmentation dependency on the energy of a primary ion beam and ToF-SIMS specific fragment ions are evaluated. It was found that the energy range approximately 6 ≤ E/n ≤ 10 eV/atom is most effective for peptide analysis based on peptide fragments and [M + H] ions. We also observed the cleaving of side chain moieties at extremely low-energy E/n ≤ 4 eV/atom.

摘要

肽或蛋白质结构分析对于生物芯片和生物设备的评估至关重要,因此需要一种能够以高横向分辨率直接从表面检测和识别蛋白质和肽种类的分析技术。在本报告中,评估了飞行时间二次离子质谱(ToF-SIMS)直接从表面分析和识别蛋白质的功效。尽管控制二次离子质谱轰击过程的物理原理使研究人员无法直接检测完整蛋白质或大于几千质量单位的较大肽段,但使用低能量单原子氩簇离子束有可能获得有关肽或蛋白质部分结构的信息。大簇离子束,如氩簇离子束和C60离子束,产生的光谱与串联质谱产生的光谱相似。二次离子质谱轰击过程还会产生传统串联质谱/质谱技术未检测到的肽片段离子。为了阐明肽结构分析的合适测量条件,评估了肽片段化对一次离子束能量的依赖性以及飞行时间二次离子质谱特定的片段离子。结果发现,基于肽片段和[M + H]离子,能量范围约为6≤E/n≤10 eV/原子对肽分析最为有效。我们还观察到在极低能量E/n≤4 eV/原子时侧链部分的裂解。

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