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Analysis of oxysterol metabolomes
Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, Volume: 1811, Issue: 11, Pages: 784 - 799
Swansea University Author: William Griffiths
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DOI (Published version): 10.1016/j.bbalip.2011.05.012
Abstract
Oxysterols are oxygenated forms of cholesterol. This definition can, however, be expanded toinclude oxygenated derivatives of plant sterols and also of cholesterol precursors. Oxysterols areformed in the first steps of cholesterol metabolism and also from cholesterol by reactive oxygenspecies. Oxyst...
Published in: | Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids |
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ISSN: | 1388-1981 |
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2011
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URI: | https://cronfa.swan.ac.uk/Record/cronfa10758 |
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2011-10-01T00:00:00.0000000 v2 10758 2012-05-21 Analysis of oxysterol metabolomes 3316b1d1b524be1831790933eed1c26e 0000-0002-4129-6616 William Griffiths William Griffiths true false 2012-05-21 MEDS Oxysterols are oxygenated forms of cholesterol. This definition can, however, be expanded toinclude oxygenated derivatives of plant sterols and also of cholesterol precursors. Oxysterols areformed in the first steps of cholesterol metabolism and also from cholesterol by reactive oxygenspecies. Oxysterols were once thought of as simple intermediates, or side-products, in the conversionof cholesterol to hormonal steroids and bile acids, however, they have subsequently been shown to bebiologically active molecules in their own right. In this article we will discuss methods of oxysterolanalysis including "classical" gas chromatography - mass spectrometry (GC-MS) methods and morerecent liquid chromatography (LC)-MS methods. Our main focus, however, will be on analyticalmethods based on "charge-tagging" and LC-tandem mass spectrometry (MS/MS or MSn) which wehave developed over the last decade in our laboratory. Examples will be given of oxysterol analysis inbrain, cerebrospinal fluid (CSF) and blood. The advantages and disadvantages of the various methodsof oxysterol analysis will be discussed. Other Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids 1811 11 784 799 1388-1981 31 12 2011 2011-12-31 10.1016/j.bbalip.2011.05.012 COLLEGE NANME Medical School COLLEGE CODE MEDS Swansea University 2011-10-01T00:00:00.0000000 2012-05-21T15:33:37.8779609 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine William Griffiths 0000-0002-4129-6616 1 Yuqin Wang 2 |
title |
Analysis of oxysterol metabolomes |
spellingShingle |
Analysis of oxysterol metabolomes William Griffiths |
title_short |
Analysis of oxysterol metabolomes |
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Analysis of oxysterol metabolomes |
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Analysis of oxysterol metabolomes |
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Analysis of oxysterol metabolomes |
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Analysis of oxysterol metabolomes |
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3316b1d1b524be1831790933eed1c26e_***_William Griffiths |
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William Griffiths |
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William Griffiths Yuqin Wang |
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Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids |
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Oxysterols are oxygenated forms of cholesterol. This definition can, however, be expanded toinclude oxygenated derivatives of plant sterols and also of cholesterol precursors. Oxysterols areformed in the first steps of cholesterol metabolism and also from cholesterol by reactive oxygenspecies. Oxysterols were once thought of as simple intermediates, or side-products, in the conversionof cholesterol to hormonal steroids and bile acids, however, they have subsequently been shown to bebiologically active molecules in their own right. In this article we will discuss methods of oxysterolanalysis including "classical" gas chromatography - mass spectrometry (GC-MS) methods and morerecent liquid chromatography (LC)-MS methods. Our main focus, however, will be on analyticalmethods based on "charge-tagging" and LC-tandem mass spectrometry (MS/MS or MSn) which wehave developed over the last decade in our laboratory. Examples will be given of oxysterol analysis inbrain, cerebrospinal fluid (CSF) and blood. The advantages and disadvantages of the various methodsof oxysterol analysis will be discussed. |
published_date |
2011-12-31T18:22:05Z |
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1821974332312649728 |
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11.048042 |