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General description
Amyloid precursor protein (APP) is an extensively studied transmembrane protein, and its derivative, amyloid β-protein, has been implicated as the primary cause of Alzheimer's disease. In the search for an effective treatment, APP is a unique model protein that illustrates the wide array of techniques available for characterization. This book presents a variety of biological techniques to elucidate the structure and function of this transmembrane protein. Each technique is presented with detailed protocols to achieve reproducible results and provide a framework for studying other membrane proteins. These protocols also form the core of the authors' approaches to elucidating the function of APP. This book contrasts methods to explain how the development of biological techniques affects the way molecular targets are examined.
Table of Contents
Antibodies to APP & Aβ Proteins
Biochemical Characterization of Amyloid Precursor Protein Assays for Analysis of APP Secretion and Recycling Strategies for Crystallizing the N-Terminal Growth Factor Domain of Amyloid Precursor Protein Analysis of Amyloid Precursor Protein Processing Protease β-Secretase: Tools For Memapsin 2 (β-Secretase) Inhibition Studies Assays for Amyloid Precursor Protein γ-Secretase Activity Cell-Free Reconstitution of β-Amyloid Production and Trafficking Studying Amyloid β-Protein Assembly Intracellular Accumulation of Amyloid β and Mitochondrial Dysfunction in Down Syndrome Linking Alzheimer's Disease, β-Amyloid, and Lipids: A Technical Approach Regulation of Amyloid Precursor Protein Processing by Lithium Immunocytochemical Analysis of Amyloid Precursor Protein and its Derivatives Pathological Detection of Aβ and APP in the Brain Creating APP Transgenic Lines in Mice Generation of Amyloid Precursor Protein Knockout Mice
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