Protein Misfolding, Aggregation and Conformational Diseases, Softcover reprint of hardcover 1st ed. 2006 Part A: Protein Aggregation and Conformational Diseases Protein Reviews Series, Vol. 4

Structural and Conformational Prerequisites of Amyloidogenesis.- Structural and Conformational Prerequisites of Amyloidogenesis.- The Generic Nature of Protein Folding and Misfolding.- The Generic Nature of Protein Folding and Misfolding.- Relative Importance of Hydrophobicity, Net Charge, and Secondary Structure Propensities in Protein Aggregation.- Relative Importance of Hydrophobicity, Net Charge, and Secondary Structure Propensities in Protein Aggregation.- Cytotoxic Intermediates in the Fibrillation Pathway: A? Oligomers in Alzheimer’s Disease as a Case Study.- Cytotoxic Intermediates in the Fibrillation Pathway: A? Oligomers in Alzheimer’s Disease as a Case Study.- Glycosaminoglycans, Proteoglycans, and Conformational Disorders.- Glycosaminoglycans, Proteoglycans, and Conformational Disorders.- Apolipoproteins in Different Amyloidoses.- Apolipoproteins in Different Amyloidoses.- Oxidative Stress and Protein Deposition Diseases.- Oxidative Stress and Protein Deposition Diseases.- Chaperone and Conformational Disorders.- Chaperone Suppression of Aggregated Protein Toxicity.- Mechanisms of Active Solubilization of Stable Protein Aggregates by Molecular Chaperones.- The Aggresome: Proteasomes, Inclusion Bodies, and Protein Aggregation.- The Aggresome: Proteasomes, Inclusion Bodies, and Protein Aggregation.- Protein Aggregation, Ion Channel Formation, and Membrane Damage.- Protein Aggregation, Ion Channel Formation, and Membrane Damage.- Visualization of Protein Deposits In Vivo.- Congo Red Staining of Amyloid: Improvements and Practical Guide for a More Precise Diagnosis of Amyloid and the Different Amyloidoses.- Immunohistological Study of Experimental Murine AA Amyloidosis.- Visualization of Protein Deposits In Vitro.- Reporters of Amyloid Structure.-Three-Dimensional Structural Analysis of Amyloid Fibrils by Electron Microscopy.- Atomic Force Microscopy.- Direct Observation of Amyloid Fibril Growth Monitored by Total Internal Reflection Fluorescence Microscopy.- Animal and Cell Models of Human Neurodegenerative Disorders.- Drosophila and C. elegans Models of Human Age-Associated Neurodegenerative Diseases.- Genetically Engineered Mouse Models of Neurodegenerative Disorders.

Fills the gap of what has not been discussed in protein review and protocol books Includes supplementary material: sn.pub/extras