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使用6 - 7微米波段中红外可调谐激光进行连续流动大气压激光解吸/电离用于生物分子质谱分析。

Continuous flow atmospheric pressure laser desorption/ionization using a 6-7-µm-band mid-infrared tunable laser for biomolecular mass spectrometry.

作者信息

Hiraguchi Ryuji, Hazama Hisanao, Senoo Kenichirou, Yahata Yukinori, Masuda Katsuyoshi, Awazu Kunio

机构信息

Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan.

JEOL Ltd., 1156 Nakagamicho, Akishima, Tokyo 196-0022, Japan.

出版信息

Int J Mol Sci. 2014 Jun 16;15(6):10821-34. doi: 10.3390/ijms150610821.

Abstract

A continuous flow atmospheric pressure laser desorption/ionization technique using a porous stainless steel probe and a 6-7-µm-band mid-infrared tunable laser was developed. This ion source is capable of direct ionization from a continuous flow with a high temporal stability. The 6-7-µm wavelength region corresponds to the characteristic absorption bands of various molecular vibration modes, including O-H, C=O, CH3 and C-N bonds. Consequently, many organic compounds and solvents, including water, have characteristic absorption peaks in this region. This ion source requires no additional matrix, and utilizes water or acetonitrile as the solvent matrix at several absorption peak wavelengths (6.05 and 7.27 µm, respectively). The distribution of multiply-charged peptide ions is extremely sensitive to the temperature of the heated capillary, which is the inlet of the mass spectrometer. This ionization technique has potential for the interface of liquid chromatography/mass spectrometry (LC/MS).

摘要

开发了一种使用多孔不锈钢探针和6-7微米波段中红外可调谐激光器的连续流动大气压激光解吸/电离技术。该离子源能够从连续流动中进行直接电离,具有很高的时间稳定性。6-7微米波长区域对应于各种分子振动模式的特征吸收带,包括O-H、C=O、CH3和C-N键。因此,许多有机化合物和溶剂,包括水,在该区域都有特征吸收峰。该离子源不需要额外的基质,而是在几个吸收峰波长(分别为6.05和7.27微米)下利用水或乙腈作为溶剂基质。多电荷肽离子的分布对作为质谱仪入口的加热毛细管的温度极为敏感。这种电离技术在液相色谱/质谱联用(LC/MS)接口方面具有潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34fc/4100183/427ce495c2f5/ijms-15-10821-g001.jpg

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