Vincent Delorme, Brigitt Raux, Rémy Puppo, Julien Leclaire, Jean-François Cavalier, Sylvain Marc, Pavan-Kumar Kamarajugadda, Gérard Buono, Frédéric Fotiadu, Stéphane Canaan, Frédéric Carrière
文献索引：Biochimie 107 Pt A , 124-34, (2014)
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A synthetic phosphonate inhibitor designed for lipase inhibition but displaying a broader range of activity was covalently immobilized on a solid support to generate a function-directed tool targeting serine hydrolases. To achieve this goal, straightforward and reliable analytical techniques were developed, allowing the monitoring of the solid support's chemical functionalization, enzyme capture processes and physisorption artifacts. This grafted inhibitor was tested on pure lipases and serine proteases from various origins, and assayed for the selective capture of lipases from several complex biological extracts. The direct identification of captured enzymes by mass spectrometry brought the proof of concept on the efficiency of this supported covalent inhibitor. The features and limitations of this "enzyme-fishing" proteomic tool provide new insight on solid-liquid inhibition process. Copyright © 2014. Published by Elsevier B.V.
