Mass spectrometry determination of endonuclear phospholipid composition and dynamics
Mass spectrometry determination of endonuclear phospholipid composition and dynamics
Mammalian cell lipid analyses using tandem electrospray ionization mass spectrometry, in conjunction with stable isotope labeling, permit unparalleled access to membrane phospholipid molecular species compositions and turnover. Lipidomic data from isolable compartments of lipid second messenger generation, such as membrane-free nuclei, can provide dynamic insights into the topology of phospholipid turnover. For example, ESI-MS/MS precursor scans of characteristic phosphocholine m/z 184+ fragments reveal a highly saturated endonuclear phosphatidylcholine pool with homeostatic maintenance properties. A spatially distinct CDPcholine pathway yields, within minutes of choline-d9 labeling, unsaturated endonuclear phosphatidylcholines progressively remodeled to more saturated species evidenced by tracking the deuteriated headgroup through precursor scans of phosphocholine-d9 (m/z 193+ fragment). Among the other endonuclear phospholipids, diacyl phosphatidylethanolamines (neutral loss of m/z 141+) are also highly saturated compared with those of whole cell whereas, phophatidylinositols (precursor scans of m/z 241? fragment) are essentially identical in nuclei and whole cells. Moreover, the pattern of myo-inositol-d6 acquisition into endonuclear phosphatidylinositol (precursor scans of m/z 247? fragment) is inconsistent with compartment-specific synthesis. Endonuclear sphingomyelins (seen in precursor scans of m/z 184+ and confirmed from precursor scans of m/z 168? fragments) are enriched but similar in composition to whole cell species whereas endonuclear phosphatidylserines (neutral loss of m/z 87?) are more saturated than their whole cell counterparts. The focus of described methodologies emphasize their value in probing the compositions and dynamics of endonuclear phospholipids, but in principle may be extended to exploration of other isolable compartments including ER or plasma membranes.
mass spectrometry, lipidomics, stable isotope, endonuclear, phosphatidylcholine, phosphatidylinositol
104-111
Hunt, Alan N.
95a3e223-da96-40e7-b47d-27dce014e305
Postle, Anthony D.
0fa17988-b4a0-4cdc-819a-9ae15c5dad66
June 2006
Hunt, Alan N.
95a3e223-da96-40e7-b47d-27dce014e305
Postle, Anthony D.
0fa17988-b4a0-4cdc-819a-9ae15c5dad66
Hunt, Alan N. and Postle, Anthony D.
(2006)
Mass spectrometry determination of endonuclear phospholipid composition and dynamics.
Methods, 39 (2), .
(doi:10.1016/j.ymeth.2006.05.005).
Abstract
Mammalian cell lipid analyses using tandem electrospray ionization mass spectrometry, in conjunction with stable isotope labeling, permit unparalleled access to membrane phospholipid molecular species compositions and turnover. Lipidomic data from isolable compartments of lipid second messenger generation, such as membrane-free nuclei, can provide dynamic insights into the topology of phospholipid turnover. For example, ESI-MS/MS precursor scans of characteristic phosphocholine m/z 184+ fragments reveal a highly saturated endonuclear phosphatidylcholine pool with homeostatic maintenance properties. A spatially distinct CDPcholine pathway yields, within minutes of choline-d9 labeling, unsaturated endonuclear phosphatidylcholines progressively remodeled to more saturated species evidenced by tracking the deuteriated headgroup through precursor scans of phosphocholine-d9 (m/z 193+ fragment). Among the other endonuclear phospholipids, diacyl phosphatidylethanolamines (neutral loss of m/z 141+) are also highly saturated compared with those of whole cell whereas, phophatidylinositols (precursor scans of m/z 241? fragment) are essentially identical in nuclei and whole cells. Moreover, the pattern of myo-inositol-d6 acquisition into endonuclear phosphatidylinositol (precursor scans of m/z 247? fragment) is inconsistent with compartment-specific synthesis. Endonuclear sphingomyelins (seen in precursor scans of m/z 184+ and confirmed from precursor scans of m/z 168? fragments) are enriched but similar in composition to whole cell species whereas endonuclear phosphatidylserines (neutral loss of m/z 87?) are more saturated than their whole cell counterparts. The focus of described methodologies emphasize their value in probing the compositions and dynamics of endonuclear phospholipids, but in principle may be extended to exploration of other isolable compartments including ER or plasma membranes.
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Published date: June 2006
Keywords:
mass spectrometry, lipidomics, stable isotope, endonuclear, phosphatidylcholine, phosphatidylinositol
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Local EPrints ID: 27173
URI: http://eprints.soton.ac.uk/id/eprint/27173
ISSN: 1046-2023
PURE UUID: bb9498aa-f7ba-4dea-a258-cbfb668ee9b3
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Date deposited: 20 Jun 2008
Last modified: 16 Mar 2024 02:48
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Author:
Alan N. Hunt
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