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紫外基质辅助激光解吸电离质谱中的基质光学吸收

Matrix Optical Absorption in UV-MALDI MS.

作者信息

Robinson Kenneth N, Steven Rory T, Bunch Josephine

机构信息

National Center of Excellence in Mass Spectrometry Imaging (NiCE-MSI), National Physical Laboratory, Teddington, UK.

Advanced Materials and Healthcare Technologies Division, University of Nottingham, Nottingham, UK.

出版信息

J Am Soc Mass Spectrom. 2018 Mar;29(3):501-511. doi: 10.1007/s13361-017-1843-4. Epub 2017 Nov 29.

Abstract

In ultraviolet matrix-assisted laser desorption/ionization mass spectrometry (UV-MALDI MS) matrix compound optical absorption governs the uptake of laser energy, which in turn has a strong influence on experimental results. Despite this, quantitative absorption measurements are lacking for most matrix compounds. Furthermore, despite the use of UV-MALDI MS to detect a vast range of compounds, investigations into the effects of laser energy have been primarily restricted to single classes of analytes. We report the absolute solid state absorption spectra of the matrix compounds α-cyano-4-hydroxycinnamic acid (CHCA), para-nitroaniline (PNA), 2-mercaptobenzothiazole (MBT), 2,5-dihydroxybenzoic acid (2,5-DHB), and 2,4,6-trihydroxyacetophenone (THAP). The desorption/ionization characteristics of these matrix compounds with respect to laser fluence was investigated using mixed systems of matrix with either angiotensin II, PC(34:1) lipid standard, or haloperidol, acting as representatives for typical classes of analyte encountered in UV-MALDI MS. The first absolute solid phase spectra for PNA, MBT, and THAP are reported; additionally, inconsistencies between previously published spectra for CHCA are resolved. In light of these findings, suggestions are made for experimental optimization with regards to matrix and laser wavelength selection. The relationship between matrix optical cross-section and wavelength-dependant threshold fluence, fluence of maximum ion yield, and R, a new descriptor for the change in ion intensity with fluence, are described. A matrix cross-section of 1.3 × 10 cm was identified as a potential minimum for desorption/ionization of analytes. Graphical Abstract ᅟ.

摘要

在紫外基质辅助激光解吸/电离质谱(UV-MALDI MS)中,基质化合物的光吸收决定了激光能量的吸收,而这又反过来对实验结果产生强烈影响。尽管如此,大多数基质化合物仍缺乏定量吸收测量。此外,尽管UV-MALDI MS可用于检测多种化合物,但对激光能量影响的研究主要局限于单一类别的分析物。我们报告了基质化合物α-氰基-4-羟基肉桂酸(CHCA)、对硝基苯胺(PNA)、2-巯基苯并噻唑(MBT)、2,5-二羟基苯甲酸(2,5-DHB)和2,4,6-三羟基苯乙酮(THAP)的绝对固态吸收光谱。使用基质与血管紧张素II、PC(34:1)脂质标准品或氟哌啶醇的混合体系,研究了这些基质化合物相对于激光能量密度的解吸/电离特性,这些混合体系分别代表了UV-MALDI MS中常见的典型分析物类别。报告了PNA、MBT和THAP的首个绝对固相光谱;此外,还解决了先前发表的CHCA光谱之间的不一致问题。鉴于这些发现,针对基质和激光波长选择的实验优化提出了建议。描述了基质光学截面与波长相关的阈值能量密度、最大离子产率能量密度以及R(一种新的离子强度随能量密度变化的描述符)之间的关系。确定了1.3×10 cm的基质截面为分析物解吸/电离的潜在最小值。图形摘要ᅟ

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