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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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