The ubiquitous roles of cytochrome P450 proteins

Sigel, Astrid and Sigel, Helmut and Sigel, Roland K. O., eds. (2007) The ubiquitous roles of cytochrome P450 proteins. Metal ions in life sciences, Vol. 3. Chichester.

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Official URL: http://edoc.unibas.ch/dok/A4087675

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Looking across the tree of life, it is amazing to find cytochrome P450 proteins represented in all life forms. Volume 3, devoted solely to the vital and still expanding research area concerning P450s, offers in 17 stimulating chapters written by 36 internationally recognized experts an authoritative and timely account of this fascinating subject. The Ubiquitous Roles of Cytochrome P450 Proteins highlights, supported by nearly 2700 references, more than 20 tables and 190 illustrations, the function of these versatile catalysts which act as monooxygenases and insert an oxygen atom from dioxygen into a substrate molecule oxidizing it. P450s are important in the biosynthesis of hormones and signaling molecules as well as in xenobiotic metabolism and detoxification ranging from pharmaceuticals in humans to toxic substances in insects and plants. Mechanistic aspects and the design and engineering of P450 systems for biotechnological applications are also covered. MILS-3 is essential for scientists working in the wide range from bioinorganic chemistry all the way through to medicine including the clinic. This volume encompasses the breadth of research efforts focused on P450s from structure to function including an appreciation of the diversity and complexity of the biotransformations they catalyze. The introductory Chapter 1, setting the scene, explores the many different levels at which these P450 enzymes (and their respective genes) have diverged in the process of evolution to yield the plethora of enzymes that are now termed "P450 monooxygenases". This broad and unprecedented reactivity of P450 enzymes which contain a heme iron center (most commonly iron(III)protoporphyrin IX) with a deprotonated cysteine side chain providing the fifth ligand to iron, has challenged the "biomimetic community". Indeed, much has been accomplished over the past five decades, e.g., regarding the understanding of the unusual activation of paramagnetic dioxygen by reductive oxygen cleavage, as is evident from Chapter 2 which provides an in depth overview of structural and functional mimics of P450s. The structures of P450 proteins and their molecular phylogeny are detailed in Chapter 3, together with the P450 nomenclature and classification. It is made clear in this account that the P450 protein fold is unique and highly conserved independent of the organism; astonishingly, the same fold is also used by some enzymes that catalyze non-P450 redox transformations. It is worthwhile to note that some P450s function at extremes of pH and heat, as was recently discovered with archaeans. The diversity of P450s is also reflected in aquatic species as is outlined in Chapter 4 where expecially P450 activities in invertebrates are in the focus. Chapter 5 examines the ability of electrochemical techniques to unravel fundamental aspects of the electron transfer process of P450 enzymes. This process is central to P450 catalysis and thus, in Chapter 6 extensive studies are summarized which have shown that interprotein electron transfer is facilitated by proper positioning, e.g., of the flavin mononucleotide- and heme-containing domains. Clearly, generation of a truly catalytic system that utilizes non-native redox cofactors in place of the reductase proteins is a holy grail of P450 research. The next four chapters center on mechanistic considerations: At first leakage reactions are considered which occur during the P450 catalytic cycle, followed by detailed evaluations of the structural basis for substrate recognition and catalysis, including the architecture of the active site. Roles of the secondary coordination sphere, i.e., at the proximal (thiolate) and the distal side (where activation of dioxygen and substrate binding occurs) are described next, as is the coordination to the heme iron of several small-molecule inhibitors like nitrogen monoxide (nitric oxide), carbon monoxide, cyanide, and imidazole. P450-catalyzed hydroxylations and epoxidations, the biosynthesis of steroid hormones, and the catalyzed carbon-carbon bond cleavage are discussed in Chapters 11–13. The design and engineering of cytochrome P450 systems is detailed in Chapter 14 regarding the oxidation of non-natural substrates. Evidently, potential applications of altered P450s in the environmentally benign synthesis of chemical products and intermediates are expected in this research area. In the terminating three chapters of The Ubiquitous Roles of Cytochrome P450 Proteins first the biotransformation of xenobiotics is comprehensively dealt with, i.e., the "chemical defence" or response of an organism to foreign chemicals. Thereafter the metabolism of drugs by human P450 systems is described, an area of particular significance for drug development and finally also for daily life in the clinic, as is emphasized by a clinical pharmacist.
Faculties and Departments:05 Faculty of Science > Departement Chemie > Chemie
UniBasel Contributors:Sigel, Helmut and Sigel, Astrid
Item Type:Book
Book Subtype:Edited Book
Bibsysno:Link to catalogue
Publisher:John Wiley
Number of Pages:652 p.
Note:Publication type according to Uni Basel Research Database: Edited book
Last Modified:22 Mar 2012 14:29
Deposited On:22 Mar 2012 14:11

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