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the lipids probably play a far more active rôle than merely functioning as a passive
matrix for the protein—which may constitute more than 50% of the membrane. The
covalent attachment of a lipid molecule to a protein, typically at a terminal amino
acid, is a significant form of post-translational modification.
It is now known that the eukaryotic lipidome typically comprises many hun-
dreds of different molecules, and their global analysis requires high-throughput
techniques. An important development has been “shotgun” mass spectrometry of
the lipids extracted by solvents,20 which not only enables the different lipids to be
identified, but also quantifies their abundances. The high throughput is achieved by
considerable automation of the process and the data handling is computationally
heavy.21
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