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      Deep-lipidotyping by mass spectrometry: recent technical advances and applications

      review-article
      1 , 2 , 2 , 1 , 2 ,
      Journal of Lipid Research
      American Society for Biochemistry and Molecular Biology
      lipidomics, tandem mass spectrometry, lipid isomers, double bond location, sn-position, glycerolipids, glycerophospholipids, branched-chain fatty acids, liquid chromatography, phenotyping, BCFA, branched-chain fatty acid, CID, collision-induced dissociation, CRF, charge-remote fragmentation, EIEIO, electron impact excitation of ions from organics, FADS2, fatty acid desaturase 2, GL, glycerolipid, GPL, glycerophospholipid, IMS, ion-mobility spectrometry, MAD, metastable atom–activated dissociation, OzID, ozone-induced dissociation, PB, Paternò-Büchi, RDD, radical-directed fragmentation, SL, sphingolipid, UVPD, ultraviolet photodissociation

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          Abstract

          In-depth structural characterization of lipids is an essential component of lipidomics. There has been a rapid expansion of mass spectrometry methods that are capable of resolving lipid isomers at various structural levels over the past decade. These developments finally make deep-lipidotyping possible, which provides new means to study lipid metabolism and discover new lipid biomarkers. In this review, we discuss recent advancements in tandem mass spectrometry (MS/MS) methods for identification of complex lipids beyond the species (known headgroup information) and molecular species (known chain composition) levels. These include identification at the levels of carbon-carbon double bond (C=C) location and sn-position, as well as characterization of acyl chain modifications. We also discuss the integration of isomer-resolving MS/MS methods with different lipid analysis workflows and their applications in lipidomics. The results showcase the distinct capabilities of deep-lipidotyping in untangling the metabolism of individual isomers and sensitive phenotyping by using relative fractional quantitation of the isomers.

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          Cellular fatty acid metabolism and cancer.

          Cancer cells often have characteristic changes in metabolism. Cellular proliferation, a common feature of all cancers, requires fatty acids for synthesis of membranes and signaling molecules. Here, we provide a view of cancer cell metabolism from a lipid perspective, and we summarize evidence that limiting fatty acid availability can control cancer cell proliferation. Copyright © 2013 Elsevier Inc. All rights reserved.
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            Phospholipase A2 enzymes: physical structure, biological function, disease implication, chemical inhibition, and therapeutic intervention.

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              Update on LIPID MAPS classification, nomenclature, and shorthand notation for MS-derived lipid structures

              A comprehensive and standardized system to report lipid structures analyzed by MS is essential for the communication and storage of lipidomics data. Herein, an update on both the LIPID MAPS classification system and shorthand notation of lipid structures is presented for lipid categories Fatty Acyls (FA), Glycerolipids (GL), Glycerophospholipids (GP), Sphingolipids (SP), and Sterols (ST). With its major changes, i.e., annotation of ring double bond equivalents and number of oxygens, the updated shorthand notation facilitates reporting of newly delineated oxygenated lipid species as well. For standardized reporting in lipidomics, the hierarchical architecture of shorthand notation reflects the diverse structural resolution powers provided by mass spectrometric assays. Moreover, shorthand notation is expanded beyond mammalian phyla to lipids from plant and yeast phyla. Finally, annotation of atoms is included for the use of stable isotope-labeled compounds in metabolic labeling experiments or as internal standards. This update on lipid classification, nomenclature, and shorthand annotation for lipid mass spectra is considered a standard for lipid data presentation.
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                Author and article information

                Contributors
                Journal
                J Lipid Res
                J Lipid Res
                Journal of Lipid Research
                American Society for Biochemistry and Molecular Biology
                0022-2275
                1539-7262
                27 April 2022
                July 2022
                27 April 2022
                : 63
                : 7
                : 100219
                Affiliations
                [1 ]State Key Laboratory of Precision Measurement Technology and Instruments, Department of Precision Instruments, Tsinghua University, Beijing, P. R. China
                [2 ]MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biological, Department of Chemistry, Tsinghua University, Beijing, P. R. China
                Author notes
                []For correspondence: Yu Xia xiayu@ 123456mail.tsinghua.edu.cn
                Article
                S0022-2275(22)00052-9 100219
                10.1016/j.jlr.2022.100219
                9213770
                35489417
                d5184778-bf34-4669-a714-1d83b5358b9d
                © 2022 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 16 March 2022
                : 19 April 2022
                Categories
                Thematic Review Series

                Biochemistry
                lipidomics,tandem mass spectrometry,lipid isomers,double bond location,sn-position,glycerolipids,glycerophospholipids,branched-chain fatty acids,liquid chromatography,phenotyping,bcfa, branched-chain fatty acid,cid, collision-induced dissociation,crf, charge-remote fragmentation,eieio, electron impact excitation of ions from organics,fads2, fatty acid desaturase 2,gl, glycerolipid,gpl, glycerophospholipid,ims, ion-mobility spectrometry,mad, metastable atom–activated dissociation,ozid, ozone-induced dissociation,pb, paternò-büchi,rdd, radical-directed fragmentation,sl, sphingolipid,uvpd, ultraviolet photodissociation

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