Phase II Conjugation Enzymes and Transport Systems

Author:

Language: English

Subjects for Phase II Conjugation Enzymes and Transport Systems

187.99 €

Subject to availability at the publisher.

Add to cartAdd to cart
Publication date:
736 p. · 15x22.8 cm · Hardback
This volume on conjugation enzymes and transporters serves to bring together current methods and concepts in an interesting, important and rapidly developing field of cell and systems biology. Phase II Conjugation Enzymes and Transport Systems focuses on the so-called Phase II enzymes of drug metabolism (xenobiotics), which has important ramifications for endogenous metabolism and nutrition. Also included are aspects on Phase III, transport systems. This volume of Methods in Enzymology presents current knowledge and methodology on glucuronidation, sulfation, acetylation, and transport systems in this field of research. Together with the volumes on Quinones and Quinone Enzymes (volumes 378 and 382), and on Glutathione Transferases and gamma-Glutamyl Transpeptidases (volume 401), the state of knowledge on proteomics and metabolomics of many pathways of (waste) product elimination, enzyme protein induction and gene regulation and feedback control is provided. This volume will help stimulate future investigations and speed the advance of knowledge in systems biology.
1 UDP-glucuronosyltransferases: Gene structures of the UGT1 and UGT2 families; 2
Identification and characterization of functional hepatocyte nuclear factor 1 binding sites in UDP-Glucuronosytransferase genes; 3 Substrate Specificity of Human Hepatic UDP-Glucuronosyltransferaes; 4 UDP-glucuronosytransferase (UGT) 1A6: structural, functional and regulatory aspects; 5 The Role of Ah Receptor in Induction of Human UDP-glucuronosyltransferase 1A1; 6 Regulation of the human UGT1A1 gene by nuclear receptors CAR, PXR and GR; 7 Isoform-selective probe substrates for in vitro studies of human UDP-glucuronosyltransferases; 8 Structure of UDP-glucuronosyltransferases in membranes; 9 Human SULT1A genes: Cloning and activity assays of the SULT1A promoters; 10 Vitamin D Receptor Regulation of the Steroid/Bile Acid Sulfotransferase SULT2A1; 11 Screening and characterizing human NAT2 variant; 12 Inactivation of human arylamine N-acetyltransferase 1 by hydrogen peroxide and peroxinitrite; 13 SULT and NAT in Mutagenicity Testing: Technical Aspects; 14 A comparative molecular field analysis (CoMFA) based approach to prediction of sulfotransferase catalytic specificity; 15 Glucuronidase deconjugation in inflammation; 16 Three-dimensional structures of sulfatases; 17 Estrogen sulfatase; 18 Analysis for localization of steroid sulfatase in human tissues; 19 Metabolism of Phytoestrogen Conjugates; 20 Coenzyme Q and phenolic conjugate metabolism; 21 Synthesis of bile acid CoA thioesters in the amino acid conjugation of bile acids; 22 Bile acid CoA: amino acid N-acyltransferase in the amino acid conjugation of bile acids; 23 Multidrug resistance protein 1-mediated export of glutathione and glutathione disulphide from brain astrocytes; 24 The genetics of ATP-binding cassette transporters; 25 Functional analysis of detergent-solubilized and membrane-reconstituted ABC Transporters; 26 Yeast ABC transporters – Cellular cleaning pumps; 27 High-speed screening of human ABC transporter function and genetic polymorphisms: New strategies in pharmacogenomics; 28 Coordinate transcriptional regulation of transport and metabolism; 29 Uptake and efflux transporters for anionic conjugates in human Hepatocytes; 30 Biliary canalicular transport systems: short-term regulation; 31 Inborn errors of biliary canalicular transport systems; 32 Epoxide Hydrolases – Structure, function, mechanism and assay; 33 Pregnane X receptor-mediated transcription; 34 Animal models of xenobiotic receptors in drug metabolism and diseases; 35 Cancer and molecular biomarkers of Phase 2
Biochemists, biophysicists, cell biologists, molecular biologists, geneticists, deverlopmental biologists
  • A laboratory standard for more than 40 years
  • Over 400 volumes strong
  • Also available on ScienceDirect