Details

Comprehensive Analysis of Parasite Biology


Comprehensive Analysis of Parasite Biology

From Metabolism to Drug Discovery
Drug Discovery in Infectious Diseases 1. Aufl.

von: Sylke Müller, Rachel Cerdan, Ovidiu Radulescu, Paul M. Selzer

160,99 €

Verlag: Wiley-Blackwell
Format: PDF
Veröffentl.: 19.07.2016
ISBN/EAN: 9783527694099
Sprache: englisch
Anzahl Seiten: 576

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Beschreibungen

Written and edited by experts in the field, this book brings together the current state of the art in phenotypic and rational, target-based approaches to drug discovery against pathogenic protozoa. The chapters focus particularly on virtual compounds and high throughput screening, natural products, computer-assisted drug design, structure-based drug design, mechanism of action identification, and pathway modelling. Furthermore, state-of the art "omics" technologies are described and currently studied enzymatic drug targets are discussed. Mathematical, systems biology-based approaches are introduced as new methodologies for dissecting complex aspects of pathogen survival mechanisms and for target identification. In addition, recently developed anti-parasitic agents targeting particular pathways, which serve as lead compounds for further drug development, are presented.
List of Contributors IX Foreword XIX Preface XXIII Part One Identification and Validation of New Drugs and Targets 1 1 Discovery of theMechanism of Action of Novel Compounds That Target Unicellular Eukaryotic Parasites 3Daniela Begolo? and Christine Clayton 2 Antiparasitics fromAlgae 41Stefan Ringgeler and Barbara Kappes? 3 Contribution of Natural Products to Drug Discovery in Tropical Diseases 75Frederick Annang, Olga Genilloud?, and Francisca Vicente 4 Isoxazolines: A Novel Chemotype Highly Effective on Ectoparasites 105Tina Weber and Paul M. Selzer? 5 Trypanosomal Cysteine Peptidases: Target Validation and Drug Design Strategies 121Elany Barbosa da Silva, Glaécia Aparecida do Nascimento Pereira, and Rafaela Salgado Ferreira? 6 Potential of Pyrimidine Metabolism for Antitrypanosomal Drug Discovery 147María Valente, Antonio E. Vidal, and Dolores González Pacanowska? 7 Phosphatidylcholine and Phosphatidylethanolamine Biosynthesis Pathways in Plasmodium 171Ewelina Guca, Alicia Contet, Henri J. Vial, KaiWengelnik, and Rachel Cerdan? 8 Immunophilins as Possible Drug Targets in Apicomplexan Parasites 193Alessandra Bianchin?, Anthony J. Chubb, and Angus Bell 9 Targeting the Atg8 Conjugation Pathway for Novel Anti-Apicomplexan Drug Discovery 213Alexia S. Miller and Jürgen Bosch? 10 Turnover of Glycosomes in Trypanosomes – Perspectives for Drug Discovery 231Ana Brennand, Eva Rico, Melisa Gualdrón-López, and Paul A.M. Michels? 11 Glideosome of Apicomplexans as a Drug Target 255Lauren E. Boucher and Jürgen Bosch? 12 N-Myristoyltransferase as a Target for Drug Discovery in Malaria 275James A. Brannigan and Anthony J. Wilkinson? Part Two Metabolomics in Drug and Target Discovery 295 13 Methods to InvestigateMetabolic Systems in Trypanosoma 297Maria Fatarova, Florian Bellvert, Edern Cahoreau, Frédéric Bringaud, and Jean-Charles Portais? 14 The Role of Metabolomics in Antiparasitic Drug Discovery 321Carlo R. Giannangelo, Katherine M. Ellis, Anna E. Sexton, Daniel Stoessel, and Darren J. Creek? 15 The Importance of Targeting Lipid Metabolism in Parasites for Drug Discovery 343Simon A. Young, Matthew D. Roberts, and Terry K. Smith? 16 CarbonMetabolism of Plasmodium falciparum 371Marco Biddau and Sylke Müller? Part Three Gene Expression and Its Regulation – A Promising Research Area for Drug Discovery 39917 Epigenetic Gene Regulation: Key to Development and Survival of Malaria Parasites 401Sabine Anne-Kristin Fraschka and Richárd Bártfai? 18 Mechanisms Regulating Transcription in Plasmodium falciparum as Targets for Novel Antimalarial Drugs 421Evelien M. Bunnik and Karine G. Le Roch? 19 Aminoacyl t-RNA Synthetases as Antimalarial Drug Targets 441Anmol Chandele? and Amit Sharma Part Four Mathematical Approaches to Drug and Target Discovery 455 20 MathematicalModeling and Omic Data Integration to Understand Dynamic Adaptation of Apicomplexan Parasites and Identify Pharmaceutical Targets 457Partho Sen, Henri J. Vial, and Ovidiu Radulescu? 21 Understanding Protozoan Parasite Metabolism and Identifying Drug Targets through Constraint-Based Modeling 487Francis Isidore Totanes, Sanu Shameer, David R.Westhead, Fabien Jourdan, and Glenn A. McConkey? 22 Attacking Blood-Borne Parasites with Mathematics 513David D. van Niekerk, Gerald Penkler, François du Toit, Jacky L. Snoep, Barbara M. Bakker, and Jurgen R. Haanstra? Index 543
"In summary, this book illustrates why it is extremely beneficial to 1) precisely understand the biology of a host–parasite unit and 2) combine a set of powerful alternative approaches for drug developmentas well as target identification and validation. In his foreword, Graham Coombs recommends that moreexperienced scientists should be encouraging those in the early stages of their career to remember appropriate past work, read books and not to forget the basic biology when applying novel approaches.I fully agree. Read this book" Prof. Dr. Marcel Deponte, Technische Universit-t Kaiserslautern, ChemMedchem, Sept 2017
Volume Editors: Prof. Sylke Muller received her PhD in 1991 from the University of Hamburg. In 1992 she worked at the London School of Hygiene and Tropical Medicine, before returning to the Bernhard Nocht Institute for Tropical Medicine in Hamburg in 1994. In 1999 she was awarded the Habilitation and the venia legendi. From 2001 to 2012 she was funded by a Wellcome Trust Senior Fellowship at Dundee University (until 2004) and the University of Glasgow (2004 to 2012). In 2006 she was awarded a Personal Chair in Molecular and Biochemical Parasitology at the University of Glasgow. Prof. Rachel Cerdan received her PhD from the University of Paris XI in 1997. She spent three years at the Laboratory of Molecular Biology (Medical Research Council) in Cambridge, UK as a Marie Curie post-doctoral fellow. She then moved to the Centre of Structural Biochemistry in Montpellier, France. In 2003, she joined the laboratory of Dynamics of Membrane Interactions in Normal and Pathological Cells in Montpellier. Currently, she is professor in biochemistry and structural biology at the University of Montpellier, France. Her current projects focus on the biochemical and structural characterization of pharmacological targets to develop new classes of antimalarials. Prof. Ovidiu Radulescu studied physics and mathematics in Bucharest and Paris and obtained his PhD in 1994 from the University of Paris XI, France. Immediately after his PhD, he worked in theoretical condensed matter physics, first in the Institute of Theoretical Physics in Nijmegen, the Netherlands, and then in the Physics Department of the University of Leeds, UK. In 1999 he joined as a lecturer the Department of Mathematics of the University of Rennes 1, France. At that time, he was also associate member of the French Institute for Research in Computer Science and Automation, INRIA. Since 2009, he is Professor in Systems Biology and team leader at the University of Montpellier, France. His team is part of the laboratory DIMNP UMR5235, whose main focuses are in parasitology and immunology. Series Editor: Prof. Paul M. Selzer studied biology, parasitology, and biochemistry at the University of Tubingen, Germany, where he also received his PhD in biochemistry. He spent three years at the Molecular Design Institute and the Parasitology and Tropical Disease Research Laboratory at the University of California, San Francisco. During his career he has worked as a researcher and scientific manager for several pharmaceutical companies, and is currently Head of Antiparasitics R&D at Boehringer Ingelheim Animal Health, Germany. He is also a visiting professor at the Interfaculty Institute of Biochemistry of the University of Tubingen, and an honorary professor of the Department of Infection, Immunity, and Inflammation at the University of Glasgow, UK.

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