New PDF release: Amyloid Proteins: Methods and Protocols

By Gal Bitan, David B. Teplow (auth.), Einar M. Sigurdsson (eds.)

ISBN-10: 1588293378

ISBN-13: 9781588293374

ISBN-10: 1592598749

ISBN-13: 9781592598748

A confirmed number of with no trouble reproducible concepts for learning amyloid proteins and their involvement within the etiology, pathogenesis, prognosis, and remedy of amyloid illnesses. The individuals offer tools for the practise of amyloid and its precursors (oligomers and protofibrils), in vitro assays and analytical suggestions for his or her learn, and telephone tradition types and assays for the construction of amyloid proteins. extra chapters current effortlessly reproducible recommendations for amyloid extraction from tissue, its detection in vitro and in vivo, in addition to nontransgenic equipment for constructing amyloid mouse types. The protocols stick with the profitable tools in Molecular Biology™ sequence structure, every one delivering step by step laboratory directions, an creation outlining the main in the back of the method, lists of the required gear and reagents, and pointers on troubleshooting and keeping off identified pitfalls.

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Extra info for Amyloid Proteins: Methods and Protocols

Sample text

We will focus on the preparation of Purification of Tau 41 PHFs from a 3-repeat and a 4-repeat tau repeat-domain construct under reducing or oxidizing conditions. Depending on whether tau isoforms or tau repeat domain constructs are used, the time frame for the in vitro preparation of bona fide paired helical filaments ranges from up to two weeks to hours, respectively. In either case, the PHF polymerization is induced by the cofactor heparin which greatly accelerates the rate and velocity of tau polymerization (see Note 7).

Biochemistry 42(26), 7871–7878. 6. , et al. (2002) alpha-Synuclein, especially the Parkinson’s diseaseassociated mutants, forms pore-like annular and tubular protofibrils. J. Mol. Biol. 322(5), 1089. 7. 7 Lashuel, H. , et al. (2002) Neurodegenerative disease: amyloid pores from pathogenic mutations. Nature 418(6895), 291. 8. 8 Ding, T. , et al. (2002) Annular alpha-synuclein protofibrils are produced when spherical protofibrils are incubated in solution or bound to brain-derived membranes. Biochemistry 41(32), 10209–10217.

Science 275(5300), 630–631. Castano, E. M. and Frangione, B. (1988) Biology of disease human amyloidosis, Alzheimer disease and related disorders. Lab. Invest. 58(2), 122–132. Selkoe, D. J. (2000) Toward a comprehensive theory for Alzheimer’s disease. Hypothesis: Alzheimer’s disease is caused by the cerebral accumulation and cytotoxicity of amyloid beta-protein. Ann. NY Acad. Sci. 924, 17–25. , et al. (1996) The profile of soluble amyloid beta protein in cultured cell media. Detection and quantification of amyloid beta protein and variants by immunoprecipitation-mass spectrometry.

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Amyloid Proteins: Methods and Protocols by Gal Bitan, David B. Teplow (auth.), Einar M. Sigurdsson (eds.)

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