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

机译:借助大型簇离子源的ToF-SIMS进行肽片段化和表面结构分析

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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 duster ion beams. Large cluster ion beams, such as Ar dusters and C-60 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 <= 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 <= 4 eV/atom.
机译:肽或蛋白质结构分析对于评估生物芯片和生物装置至关重要,因此需要一种能够直接从横向分辨率高的表面检测和鉴定蛋白质和肽种类的分析技术。在本报告中,评估了ToF-SIMS直接从表面分析和鉴定蛋白质的功效。尽管控制SIMS轰击过程的物理学使研究人员无法直接检测完整的蛋白质或数千个质量单位以上的较大肽,但仍可以使用低能量的每原子氩来获得有关肽或蛋白质部分结构的信息除尘离子束。大型簇离子束(例如Ar喷粉器和C-60离子束)产生的光谱类似于串联MS产生的光谱。 SIMS轰击过程还会产生常规MS / MS技术无法检测到的肽片段离子。为了阐明用于肽结构分析的适当测量条件,评估了肽片段化对一次离子束和ToF-SIMS特定片段离子的能量的依赖性。已经发现,基于肽片段和[M + H]离子,大约6 <= E / n <= 10 eV / atom的能量范围最有效。我们还观察到以极低的能量E / n <= 4 eV / atom裂解侧链部分。

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