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Affinity surface-assisted laser desorption/ionization mass spectrometry for peptide enrichment

机译:亲和性表面辅助激光解吸/电离质谱用于富集肽

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摘要

In this paper, we report on the functionalization of silicon nanostructured(NanoSi)surface with an organic layer of nitrilotriacetic acid(NTA)and its subsequent use as an affinity surface-assisted laser desorption/ionization mass spectrometry(SALDI-MS)interface for histidine-tagged peptide enrichment and mass spectrometry analysis. The NTA terminal groups are immobilized onto the NanoSi surface via very stable Si-C covalent bonds. The NTA-modified NanoSi(NTA-NanoSi)interface was characterized by contact angle measurements, Fourier transform infrared(FTIR)spectroscopy and X-ray photoelectron spectroscopy(XPS). The NTA-NanoSi interface has shown a good selectivity toward His-tagged peptide and permits its enrichment from an artificial mixture of both tagged and untagged peptides and its subsequent mass spectrometry detection with good signaloise ratio.
机译:在本文中,我们报道了具有次氮基三乙酸(NTA)有机层的硅纳米结构(NanoSi)表面的功能化及其随后用作组氨酸的亲和表面辅助激光解吸/电离质谱(SALDI-MS)接口的用途标记的肽富集和质​​谱分析。 NTA末端基团通过非常稳定的Si-C共价键固定在NanoSi表面上。通过接触角测量,傅立叶变换红外(FTIR)光谱和X射线光电子能谱(XPS)表征了NTA改性的NanoSi(NTA-NanoSi)界面。 NTA-NanoSi界面对His标记的肽表现出良好的选择性,并允许从标记和未标记的肽的人工混合物中富集,并随后以良好的信噪比进行质谱检测。

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