From simple to supramolecular cytochrome P450 mimics

Citation
Mc. Feiters et al., From simple to supramolecular cytochrome P450 mimics, CHEM SOC RE, 29(6), 2000, pp. 375-384
Citations number
88
Categorie Soggetti
Chemistry
Journal title
CHEMICAL SOCIETY REVIEWS
ISSN journal
03060012 → ACNP
Volume
29
Issue
6
Year of publication
2000
Pages
375 - 384
Database
ISI
SICI code
0306-0012(200011)29:6<375:FSTSCP>2.0.ZU;2-B
Abstract
Cytochrome P450 is one of Nature's oxidative workhorses and is utilized in a wide variety of roles, one of the most important being the detoxification of foreign bodies within the liver. As a result of its fundamental importa nce it has been extensively investigated, modeled and mimicked over the pas t 30 years, and more recently modified and mutated. During this period the complexity, beauty and activity of the biomimetic model systems developed i n the laboratory have grown considerably. The synthetic analogues of the cy tochrome P450 system have evolved dramatically fromsimple sterically hinder ed porphyrin models through to more complex model systems combining cavitie s such as cyclodextrins and utilizing the interactions between host and gue st to generate substrate selectivity and stereoselectivity in product forma tion. More recently, researchers have tried to combine knowledge obtained f rom the developing field of supramolecular chemistry and from biochemistry to construct self-assembling systems that contain all the components of the natural system and even utilize molecular oxygen as the oxidant. These sys tems are successful in that they can achieve turnover numbers comparable to those observed for the natural system. The history of these developments a nd the current 'state-of-the-art' in construction of mimics of the natural enzyme will be presented.