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在非均匀样品的基质辅助激光解吸/电离中获取深度剖析和可重现质谱。

Acquisition of the depth profiles and reproducible mass spectra in matrix-assisted laser desorption/ionization of inhomogeneous samples.

作者信息

Ahn Sung Hee, Park Kyung Man, Moon Jeong Hee, Lee Seong Hoon, Kim Myung Soo

机构信息

Department of Chemistry, Seoul National University, Seoul, 151-747, Korea.

Medical Proteomics Research Center, KRIBB, Daejeon, 305-806, Korea.

出版信息

Rapid Commun Mass Spectrom. 2015 Apr 30;29(8):745-52. doi: 10.1002/rcm.7157.

DOI:10.1002/rcm.7157
PMID:26406489
Abstract

RATIONALE

In our previous analysis of the matrix-assisted laser desorption/ionization (MALDI) spectra of peptides, we treated their depth profiles in solid samples as homogeneous. Here, we wanted to determine if the reproducible MALDI spectra and linear calibration curves reported previously would be obtained even when the depth profiles were inhomogeneous.

METHODS

We derived a formula relating shot-number-dependent ion abundance data in temperature-controlled MALDI with the analyte depth profile in a solid sample. We prepared samples containing peptides, amino acids, and serotonin in α-cyano-4-hydroxycinnamic acid matrix by vacuum-drying and micro-spotting methods, recorded their MALDI spectra, and analyzed them with the aforementioned formula.

RESULTS

For the samples prepared by vacuum-drying, the analyte depth profiles were inhomogeneous and maximized at the sample surface. Although the MALDI spectra changed as the shot continued, their sum over the entire set of spectra acquired from a spot was reproducible. Similarly, a high-quality calibration curve could be obtained with the spectral data summed over the entire set. Depth profiles were homogeneous for samples prepared by micro-spotting.

CONCLUSIONS

A method has been developed to obtain a reproducible MALDI spectrum and a linear calibration curve for an analyte with an inhomogeneous depth profile in a solid sample.

摘要

原理

在我们之前对肽的基质辅助激光解吸/电离(MALDI)光谱的分析中,我们将其在固体样品中的深度分布视为均匀的。在此,我们想确定即使深度分布不均匀,之前报道的可重现的MALDI光谱和线性校准曲线是否仍能获得。

方法

我们推导了一个公式,将温度控制的MALDI中与发射次数相关的离子丰度数据与固体样品中分析物的深度分布联系起来。我们通过真空干燥和微斑点法制备了含有肽、氨基酸和血清素的α-氰基-4-羟基肉桂酸基质样品,记录其MALDI光谱,并用上述公式进行分析。

结果

对于通过真空干燥制备的样品,分析物深度分布不均匀且在样品表面达到最大值。尽管随着发射次数的持续,MALDI光谱会发生变化,但从一个斑点获取的整个光谱集的总和是可重现的。同样,对整个光谱集的数据求和可得到高质量的校准曲线。通过微斑点法制备的样品深度分布是均匀的。

结论

已开发出一种方法,可在固体样品中为深度分布不均匀的分析物获得可重现的MALDI光谱和线性校准曲线。

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引用本文的文献

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Investigations of Some Liquid Matrixes for Analyte Quantification by MALDI.用于基质辅助激光解吸电离(MALDI)分析物定量的一些液体基质的研究。
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