Buch, Englisch, Band 32, 408 Seiten, Format (B × H): 157 mm x 235 mm, Gewicht: 1760 g
Methods and Protocols
Buch, Englisch, Band 32, 408 Seiten, Format (B × H): 157 mm x 235 mm, Gewicht: 1760 g
Reihe: Methods in Molecular Medicine
ISBN: 978-0-89603-737-3
Verlag: Humana Press
Alzheimer's disease is the most common cause of senile dementia. Since the discovery in 1984 of the amyloid ?-peptide (A?) as the core protein of the senile plaques present in the brains of Alzheimer's disease sufferers, an immense amount of research has gone into mapping out the molecular basis of this debilitating disease. The aim of Alzheimer's Disease: Methods and Protocols is to bring together the main biochemical, cell biological, and molecular biological techniques and approaches that are being used to investigate the molecular basis of Alzheimer's disease. This volume begins with chapters of an introductory/ review nature. Chapter 1 provides a historical introduction to Alzheimer's d- ease with particular emphasis on the central role played by A? and its re- tion to tau. Chapter 2 examines the genetics underlying this neurodegenerative disease, covering the amyloid precursor protein, apolipoprotein E, and the presenilins. Chapter 3 presents an overview of currently available therapeutic agents and prospects for drugs of the future.
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to Alzheimer's Disease.- The Genetics of Alzheimer's Disease.- Advances in Methodology and Current Prospects for Primary Drug Therapies for Alzheimer's Disease.- Production and Functional Assays of Recombinant Secreted Amyloid Precursor Protein (APP) (sAPP?).- Quantifying A?1–40 and A?1–42 Using Sandwich-ELISA.- Electrophoretic Separation and Immunoblotting of A?1–40 and A?1–42.- A?-Induced Proinflammatory Cytokine Release from Differentiated Human THP-1 Monocytes.- Effects of the ?-Amyloid Peptide on Membrane Ion Permeability.- Analysis of ?-Amyloid Peptide Degradation In Vitro.- Posttranslational Modifications of Amyloid Precursor Protein.- Posttranslational Modifications of the Amyloid Precursor Protein.- Using an Amyloid Precursor Protein (APP) Reporter to Characterize ?-Secretase.- Inhibition of ?-Secretase by Zinc Metalloproteinase Inhibitors.- Development of Neoepitope Antibodies Against the ?-Secretase Cleavage Site in the Amyloid Precursor Protein.- ?-Secretase.- Using ?-Secretase Inhibitors to Distiguish the Generation of the A? Peptides Terminating at Val-40 and Ala-42.- Designing Animal Models of Alzheimer's Disease with Amyloid Precursor Protein (APP) Transgenes.- Phosphorylation of Amyloid Precursor Protein (APP) Family Proteins.- Determining the Transmembrane Topology of the Presenilins.- Normal Proteolytic Processing of the Presenilins.- Apoptotic Proteolytic Cleavage of the Presenilins by Caspases.- The Phosphorylation of Presenilin Proteins.- Interaction of the Presenilins with the Amyloid Precursor Protein (APP).- Distribution of Presenilins and Amyloid Precursor Protein (APP) in Detergent-Insoluble Membrane Domains.- Characterization and Use of Monoclonal Antibodies to Tau and Paired Helical Filament Tau.- Tau PhosphorylationBoth In Vitro and in Cells.- Transglutaminase-Catalyzed Formation of Alzheimer-Like Insoluble Complexes from Recombinant Tau.
