Department of Chemistry, University of Florida, Gainesville, Florida 32611, United States.
Anal Chem. 2021 Apr 27;93(16):6311-6322. doi: 10.1021/acs.analchem.1c00061. Epub 2021 Apr 15.
Lipids and metabolites are of interest in many clinical and research settings because it is the metabolome that is increasingly recognized as a more dynamic and sensitive molecular measure of phenotype. The enormous diversity of lipid structures and the importance of biological structure-function relationships in a wide variety of applications makes accurate identification a challenging yet crucial area of research in the lipid community. Indeed, subtle differences in the chemical structures of lipids can have important implications in cellular metabolism and many disease pathologies. The speed, sensitivity, and molecular specificity afforded by modern mass spectrometry has led to its widespread adoption in the field of lipidomics on many different instrument platforms and experimental workflows. However, unambiguous and complete structural identification of lipids by mass spectrometry remains challenging. Increasingly sophisticated tandem mass spectrometry (MS/MS) approaches are now being developed and seamlessly integrated into lipidomics workflows to meet this challenge. These approaches generally either (i) alter the type of ion that is interrogated or (ii) alter the dissociation method in order to improve the structural information obtained from the MS/MS experiment. In this Perspective, we highlight recent advances in both ion type alteration and ion dissociation methods for lipid identification by mass spectrometry. This discussion is aimed to engage investigators involved in fundamental ion chemistry and technology developments as well as practitioners of lipidomics and its many applications. The rapid rate of technology development in recent years has accelerated and strengthened the ties between these two research communities. We identify the common characteristics and practical figures of merit of these emerging approaches and discuss ways these may catalyze future directions of lipid structural elucidation research.
脂质和代谢物在许多临床和研究环境中都很重要,因为越来越多的人认为代谢组学是表型更具动态性和敏感性的分子测量指标。脂质结构的多样性以及在各种应用中生物结构-功能关系的重要性,使得准确识别成为脂质领域研究中具有挑战性但至关重要的领域。事实上,脂质化学结构的细微差异可能对细胞代谢和许多疾病病理有重要影响。现代质谱技术具有速度快、灵敏度高和分子特异性强的特点,已在许多不同的仪器平台和实验工作流程中广泛应用于脂质组学领域。然而,通过质谱对脂质进行明确和完整的结构鉴定仍然具有挑战性。越来越复杂的串联质谱(MS/MS)方法现在正在开发中,并无缝集成到脂质组学工作流程中,以应对这一挑战。这些方法通常要么(i)改变被探测的离子类型,要么(ii)改变解离方法,以提高从 MS/MS 实验中获得的结构信息。在本观点中,我们重点介绍了近年来在通过质谱进行脂质鉴定中改变离子类型和离子解离方法方面的最新进展。这一讨论旨在让从事基础离子化学和技术发展的研究人员以及脂质组学及其众多应用的从业者参与进来。近年来技术发展的快速步伐加速并加强了这两个研究社区之间的联系。我们确定了这些新兴方法的共同特点和实用基准,并讨论了这些方法如何为未来的脂质结构阐明研究方向提供催化作用。