<p>This monograph is dedicated to one of the discoverers of poly(ADPยญ ribose), Professor Paul Mandel, from the Centre de Neurochimie in Strasbourg. We would like to congratulate him for his distinguished contributions to the field of poly(ADP-ribosyl)ation and express our gratitude for his support i
ADP-Ribosylating Toxins
โ Scribed by I. H. Madshus, H. Stenmark (auth.), Professor Dr. Dr. Klaus Aktories (eds.)
- Publisher
- Springer-Verlag Berlin Heidelberg
- Year
- 1992
- Tongue
- English
- Leaves
- 153
- Series
- Current Topics in Microbiology and Immunology 175
- Edition
- 1
- Category
- Library
No coin nor oath required. For personal study only.
โฆ Synopsis
ADP-ribosylating toxins have been the focus of intensive research for more than 30 years. Researchers from diverse fields of science have taken an interest in these bacterial toxins; they are studied, for example, by microbiologists, biochemists, cell biologists, and pharmacologists. There are two principal reasons for the broad and still growing interest in ADPยญ ribosylating toxins. First, insights into the structure and functions of the toxins might be the key to prevention and treatment of diseases caused by the toxin-producing infectious microยญ organisms. Second, the ADP-ribosylating toxins provide potent and often unique pharmacological tools for the study of the physiological functions of their target proteins. The latter is especially the case with cholera and pertussis toxins, which both modify the IX-subunits of heterotrimeric G-proteins involved in signal transduction pathways. These toxins have proved invaluable in extending our basic understanding of the regulation of hormone-controlled signal transduction. This volume provides a review and an update of recent studies on the basic properties of bacterial ADP-ribosylating tbxins and/or exoenzymes. Our current knowledge of the celยญ lular entry mechanisms of ADP-ribosylating toxins is reviewed by MADSHUS and STENMARK. WILSON and COLLIER then deal with recent insights into the enzyme mechanism and active site structure of diphtheria toxin and Pseudomonas aeruginosa exotoxin A, which modify elongation factor 2. Toxins which ADP-ribosylate heterotrimeric G-proteins involved in transยญ membrane signal transduction are the subject of the next two chapters.
โฆ Table of Contents
Front Matter....Pages I-X
Entry of ADP-Ribosylating Toxins into Cells....Pages 1-26
Diphtheria Toxin and Pseudomonas aeruginosa Exotoxin A: Active-Site Structure and Enzymic Mechanism....Pages 27-41
Enhancement of Cholera Toxin-Catalyzed ADP-Ribosylation by Guanine Nucleotide-Binding Proteins....Pages 43-67
ADP-Ribosylation of Signal-Transducing Guanine Nucleotide-Binding Proteins by Pertussis Toxin....Pages 69-96
Clostridial Actin-ADP-Ribosylating Toxins....Pages 97-113
Clostridium botulinum C3 ADP-Ribosyltransferase....Pages 115-131
Pseudomonas aeruginosa Exoenzyme S....Pages 133-143
Back Matter....Pages 145-150
โฆ Subjects
Medical Microbiology
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