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低于衍射极限的红外质谱成像

Infrared mass spectrometric imaging below the diffraction limit.

作者信息

Luxembourg Stefan L, McDonnell Liam A, Mize Todd H, Heeren Ron M A

机构信息

FOM Institute for Atomic and Molecular Physics, Kruislaan 407, 1098 SJ Amsterdam, The Netherlands.

出版信息

J Proteome Res. 2005 May-Jun;4(3):671-3. doi: 10.1021/pr049762+.

Abstract

Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS)1 is an established technique for the analysis of biological macromolecules. Its relative insensitivity to pollutants makes MALDI-MS very suitable for the direct analysis of biological samples. As such, it has facilitated great advances in the field of biomolecular imaging mass spectrometry. Traditionally, MALDI-MS imaging is performed in a scanning microprobe methodology.(2-4) However, in a recent study we have demonstrated an alternative methodology; the so-called microscope mode,(5) where the requirement for a highly focused ionization beam is removed. Spatial details from within the desorption area are conserved during the flight of the ions through the mass analyzer, and a magnified ion image is projected onto a 2D-detector. In this paper, we demonstrate how imaging mass spectrometry benefits from the microscope mode approach. For the first time, high-lateral resolution ion images were recorded using infrared MALDI at 2.94 microm wavelength. The ion optical resolution achieved was well below the theoretical limit of (light-) diffraction for the setup used, which is impossible to achieve in the conventional scanning microprobe approach.

摘要

基质辅助激光解吸/电离质谱(MALDI-MS)1是一种用于分析生物大分子的成熟技术。它对污染物相对不敏感,这使得MALDI-MS非常适合直接分析生物样品。因此,它推动了生物分子成像质谱领域的巨大进步。传统上,MALDI-MS成像采用扫描微探针方法进行。(2-4)然而,在最近的一项研究中,我们展示了另一种方法;即所谓的显微镜模式,(5)在这种模式下,不再需要高度聚焦的电离束。离子在通过质量分析器飞行过程中,解吸区域内的空间细节得以保留,并且放大的离子图像被投射到二维探测器上。在本文中,我们展示了成像质谱如何从显微镜模式方法中受益。首次使用波长为2.94微米的红外MALDI记录了高横向分辨率的离子图像。所实现的离子光学分辨率远低于所用装置的(光)衍射理论极限,这在传统扫描微探针方法中是无法实现的。

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