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环境条件下用于空间分辨组织蛋白质组学的底物介导激光烧蚀

Substrate-Mediated Laser Ablation under Ambient Conditions for Spatially-Resolved Tissue Proteomics.

作者信息

Fatou Benoit, Wisztorski Maxence, Focsa Cristian, Salzet Michel, Ziskind Michael, Fournier Isabelle

机构信息

Univ. Lille, INSERM, U1192 - Laboratoire Protéomique, Réponse Inflammatoire et Spectrométrie de Masse-PRISM, F-59000 Lille, France.

Univ. Lille, CNRS, UMR 8523 - PhLAM - Physique des Lasers Atomes et Molécules, F-59000 Lille, France.

出版信息

Sci Rep. 2015 Dec 17;5:18135. doi: 10.1038/srep18135.

Abstract

Numerous applications of ambient Mass Spectrometry (MS) have been demonstrated over the past decade. They promoted the emergence of various micro-sampling techniques such as Laser Ablation/Droplet Capture (LADC). LADC consists in the ablation of analytes from a surface and their subsequent capture in a solvent droplet which can then be analyzed by MS. LADC is thus generally performed in the UV or IR range, using a wavelength at which analytes or the matrix absorb. In this work, we explore the potential of visible range LADC (532 nm) as a micro-sampling technology for large-scale proteomics analyses. We demonstrate that biomolecule analyses using 532 nm LADC are possible, despite the low absorbance of biomolecules at this wavelength. This is due to the preponderance of an indirect substrate-mediated ablation mechanism at low laser energy which contrasts with the conventional direct ablation driven by sample absorption. Using our custom LADC system and taking advantage of this substrate-mediated ablation mechanism, we were able to perform large-scale proteomic analyses of micro-sampled tissue sections and demonstrated the possible identification of proteins with relevant biological functions. Consequently, the 532 nm LADC technique offers a new tool for biological and clinical applications.

摘要

在过去十年中,常压质谱(MS)已展现出众多应用。这些应用推动了各种微采样技术的出现,如激光烧蚀/液滴捕获(LADC)。LADC包括从表面烧蚀分析物,随后将其捕获在溶剂液滴中,然后可通过质谱进行分析。因此,LADC通常在紫外或红外范围内进行,使用分析物或基质吸收的波长。在这项工作中,我们探索了可见光范围LADC(532nm)作为大规模蛋白质组学分析微采样技术的潜力。我们证明,尽管生物分子在该波长下吸光度较低,但使用532nm LADC进行生物分子分析是可行的。这是由于在低激光能量下间接底物介导的烧蚀机制占主导地位,这与由样品吸收驱动的传统直接烧蚀形成对比。使用我们定制的LADC系统并利用这种底物介导的烧蚀机制,我们能够对微采样的组织切片进行大规模蛋白质组学分析,并证明了可能鉴定出具有相关生物学功能的蛋白质。因此,532nm LADC技术为生物学和临床应用提供了一种新工具。

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