[环境电离质谱法在油脂鉴定中的应用进展]。

Xiao-Rong Wang, Yi-Yan Yin, Jin Ouyang, Na Na
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引用次数: 0

摘要

脂质是生物体不可缺少的组成部分,在细胞膜流动性、能量供应和神经递质传递和运输中起着关键作用。由于脂质具有指示细胞生长状态的能力,因此可以作为疾病的潜在生物标志物。例如,由于癌细胞的快速增殖和对不断变化的生物环境的适应,它们的脂质代谢过程与正常细胞不同。因此,快速检测、识别和监测脂质成分的能力对于跟踪生命相关过程至关重要,并可能提高癌症的诊断和治疗效果。质谱(MS)被认为是直接获得分子结构信息的最有效方法之一,在鉴定脂质方面具有明显的优势。近年来出现了环境质谱(AMS),它可以直接对分析物进行采样和电离,而无需进行样品预处理。这些特点赋予了AMS在识别和监测血脂方面的特殊优势。此外,软电离技术的不断发展导致AMS广泛用于检测复杂和多样的脂质分子。电喷雾电离(ESI)是一种温和的电离方法,可用于检测中至高极性化合物,并通过从液体样品中产生带电液滴的细雾来提供详细的脂质化学信息。因此,已经开发了一系列基于esi的电离方法,用于制造能够以简单的方式快速检测脂质的不同AMS系统。例如,解吸电喷雾电离(DESI)是应用最广泛的环境电离技术之一,已被用于检测各种样品,包括固体、液体和气体。DESI包括在样品表面喷洒带电溶剂,之后溶剂被解吸,分析物被电离,产生的离子通过气体羽流转移到质谱仪的检测器。DESI可以方便、精确地调节采样空间,从而为原位检测组织样品中的脂质提供了一种高效的方法。此外,单细胞脂质分析受限于细胞体积小,细胞基质复杂,分析物的绝对量最小。常用的单细胞检测方法有流式细胞术和荧光显微镜,这两种方法都需要荧光标记来检测特定的靶分子,这在一定程度上限制了检测的选择性和重复性。基于esi的单细胞质谱法由于其高灵敏度、低样品消耗、高通量和多重检测能力等优点,已成为一种更有效的细胞脂质检测方法。此外,脂质化学多样性对确定结构细节提出了重大挑战。因此,基于ams的脂质检测已经通过一系列化学处理方法得到增强,这些方法可以提供更全面的脂质结构信息。例如,不同的气相分离技术已被用于区分脂质C=C键异构体及其sn位置。在质谱检测之前,还采用了化学修饰特定目标C=C键的策略。例如,Paternò-Büchi (P-B)光化学反应将不饱和脂质的C=C键氧化形成氧烷结构,C=C键可被环氧化形成相应的杂氮嘧啶,N-H氮化反应将C=C键转化为叠氮嘧啶,1ΔO2烯反应在C=C键上加入OOH基团。在这篇综述中,我们讨论了近五年来发展的各种脂质AMS环境电离技术,重点介绍了用于分析脂质精细结构的典型化学策略。尽管基于质谱的脂质检测技术取得了显著进步,但基于质谱的高覆盖、高灵敏度脂质检测平台仍然具有挑战性,需要进一步深入研究。
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[Progress in applications of ambient ionization mass spectrometry for lipids identification].

Lipids are indispensable components of living organisms and play pivotal roles in cell-membrane fluidity, energy provision, and neurotransmitter transmission and transport. Lipids can act as potential biomarkers of diseases given their abilities to indicate cell-growth status. For example, the lipid-metabolism processes of cancer cells are distinct from those of normal cells owing to their rapid proliferation and adaptation to ever-changing biological environments. As a result, the ability to rapidly detect, identify, and monitor lipid components is critical for tracking life-related processes and may enhance cancer diagnosis and treatment efficacy. Mass spectrometry (MS) is regarded to be among the most efficient methods for directly obtaining molecular-structural information, and is distinctly advantageous for identifying lipids. Recent years have witnessed the emergence of ambient mass spectrometry (AMS), which enables direct analyte sampling and ionization without the need for sample preprocessing. These characteristics endow AMS with special advantages for identifying and monitoring lipids. Furthermore, the ongoing development of soft ionization technologies has led to the widespread use of AMS for the detection of complex and diverse lipid molecules. Electrospray ionization (ESI) is a gentle ionization method that can be used to detect medium-to-high-polarity compounds and provide detailed chemical information for lipids by producing a fine mist of charged droplets from a liquid sample. Consequently, a series of ESI-based ionization methods have been developed for fabricating different AMS systems capable of rapidly detecting lipids in a simple manner. For example, desorption electrospray ionization (DESI) is among the most extensively employed ambient ionization techniques, and has been used to detect a wide range of samples, including solids, liquids, and gases. DESI involves spraying a charged solvent onto the surface of a sample, after which the solvent is desorbed, the analyte is ionized, and the generated ions are transferred to the detector of the mass spectrometer via a gas plume. DESI can easily and precisely regulate the sampling space, thereby offering a highly effective approach for the in-situ detection of lipids from tissue samples. Additionally, single-cell lipid analysis is limited by small cell volumes, complex cellular matrices, and minimal absolute amounts of analyte. Common detection methods for single cells include flow cytometry and fluorescence microscopy, both of which require fluorescent labeling to detect specific target molecules, which limits detection selectivity and reproducibility to some extent. ESI-based single-cell mass spectrometry has emerged as a more-effective method for detecting cellular lipids owing to advantages that include high sensitivity, low sample consumption, high throughput, and multiple-detection capabilities. Moreover, lipid chemical diversity poses a significant challenge for determining structural details. Therefore, AMS-based lipid detection has been augmented with a series of chemical-treatment methods that provide more-comprehensive structural information for lipids. For example, diverse gas-phase dissociation techniques have been used to discriminate between lipid C=C-bond isomers and their sn-positions. Strategies that involve chemically modifying specific target C=C bonds prior to MS detection have also been employed. For example, the Paternò-Büchi (P-B) photochemical reaction oxidizes C=C bonds in unsaturated lipids to form oxetane structures, C=C bonds can be epoxidized to form the corresponding oxaziridines, the N-H aziridination reaction converts C=C bonds into aziridines, and the 1ΔO2 ene reaction adds an OOH group to a C=C bond. In this review, we discuss various environmental ionization techniques for lipid AMS developed over the past five years, with an emphasis on typical chemical strategies used to analyze lipid fine structures. Obtaining a high-coverage, high-sensitivity lipid-detection platform based on AMS remains challenging and requires further in-depth studies despite significant improvements in lipid MS-based detection techniques.

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