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Improved Photocontrol of α-Chymotrypsin Activity: Peptidomimetic Trifluoromethylketone Photoswitch Enzyme Inhibitors

✍ Scribed by David Pearson; Nathan Alexander; Andrew D. Abell


Book ID
101832704
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
310 KB
Volume
14
Category
Article
ISSN
0947-6539

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✦ Synopsis


Abstract

A series of peptidomimetic trifluoromethylketones containing the photoisomerisable azobenzene group have been synthesised, photoisomerised and assayed against the serine protease α‐chymotrypsin. All are inhibitors of the enzyme and exhibit up to a fivefold increase in activity on UV irradiation. Visible irradiation returns activity to close to that of the original sample. These results suggest the trifluoromethylketone group to be the best electrophilic enzyme binding group for use in photoswitch inhibitors of α‐chymotrypsin.


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