Department of Chemistry and Bindley Bioscience Center, Purdue University, West Lafayette, Indiana 47907, United States.
Acc Chem Res. 2023 Sep 19;56(18):2526-2536. doi: 10.1021/acs.accounts.3c00382. Epub 2023 Sep 6.
Mass spectrometry (MS) is one of the most widely used technologies in the chemical sciences. With applications spanning the monitoring of reaction products, the identification of disease biomarkers, and the measurement of thermodynamic parameters and aspects of structural biology, MS is well established as a universal analytical tool applicable to small compounds as well as large molecular complexes. Regardless of the application, the generation of gas-phase ions from neutral compounds is a key step in any MS experiment. However, this ionization step was for many years limited to high-energy approaches that required gas-phase analytes and thus it was restricted to volatile samples. Over the last few decades, new methodologies have been developed to address this limitation and facilitate ionization of biological molecules. Electrospray ionization (ESI) is the most broadly used of these methods, as it facilitates the ionization of intact polar compounds from solution. Twenty years ago, our group reported a new ionization method that uses a charged solvent spray to impact a surface, generating ions from rather than just and doing so directly in the ambient environment with no vacuum requirements and little to no sample preparation. This method was termed desorption electrospray ionization (DESI), and it initiated a new field that would come to be known as ambient mass spectrometry. The simplicity and wide applicability of the DESI technology—and the tens of ambient ionization methods developed subsequently—revolutionized the MS analysis of complex materials for their organic components, especially for applications. This Account describes the history of DESI, starting with the development of the technique from early electrosonic spray ionization (ESSI) experimental observations as well as the studies leading to the understanding of its mechanism as a “droplet pick-up” phenomenon involving sequential events (, thin film formation, solid–liquid extraction, secondary droplet generation, and ESI-like ionization from these droplets). We also overview the developments and applications of the technology that have been demonstrated by our group during the last two decades. In particular, we describe (i) the use of DESI for tissue imaging, one of its more significant applications to date, and its extension to intraoperative clinical diagnosis; (ii) the integration of the technology with portable instrumentation for analysis, especially when coupled with tandem mass spectrometry (MS/MS); (iii) the use of DESI microdroplets as microvessels to accelerate organic reactions by orders of magnitude compared to those in bulk solution; and (iv) the combination of all these capabilities for automated high-throughput experiments aimed at accelerating drug discovery.
质谱 (MS) 是化学科学中应用最广泛的技术之一。其应用涵盖了反应产物的监测、疾病生物标志物的鉴定以及热力学参数和结构生物学方面的测量,MS 已成为一种通用的分析工具,适用于小分子以及大分子复合物。无论应用如何,将中性化合物转化为气相离子是任何 MS 实验的关键步骤。然而,多年来,这种离子化步骤仅限于需要气相分析物的高能方法,因此它仅限于易挥发的样品。在过去的几十年中,已经开发出了新的方法来解决这一限制,并促进生物分子的离子化。电喷雾电离 (ESI) 是最广泛使用的方法之一,因为它可以促进极性化合物从溶液中整体的离子化。二十年前,我们小组报告了一种新的离子化方法,该方法使用带电溶剂喷雾冲击表面,直接在环境中生成而不是仅从生成离子,并且无需真空要求,也无需进行大量的样品制备。该方法被称为解吸电喷雾电离 (DESI),它开创了一个新的领域,即所谓的环境质谱学。DESI 技术的简单性和广泛适用性——以及随后开发的数十种环境离子化方法——彻底改变了复杂材料中有机成分的 MS 分析,特别是在应用方面。本综述描述了 DESI 的历史,从早期的电声喷雾电离 (ESSI) 实验观察到该技术的发展开始,并介绍了导致其机制理解的研究,其机制是一种涉及连续事件的“液滴提取”现象(,薄膜形成、固-液萃取、二次液滴生成以及来自这些液滴的 ESI 样离子化)。我们还概述了过去二十年我们小组展示的该技术的发展和应用。特别是,我们描述了 (i) DESI 在组织成像中的应用,这是其迄今为止最重要的应用之一,以及它在术中临床诊断中的扩展;(ii) 将该技术与便携式仪器集成用于分析,尤其是与串联质谱 (MS/MS) 结合时;(iii) 使用 DESI 微液滴作为微容器,使有机反应的速度比在本体溶液中快几个数量级;以及 (iv) 结合所有这些功能,实现自动化高通量实验,以加速药物发现。