Protein misfolding diseases methods and protocols - Gomes, Cláudio M. 1970- (Springer New York, 2019)
Biophysical and Spectroscopic Methods for Monitoring Protein Misfolding and Amyloid Aggregation – Ultrasensitive RT-QuIC Seed Amplification Assays for Disease-Associated Tau, α-Synuclein, and Prion Aggregates – Vesicle-Based Assays to Study Membrane Interactions of Amyloid Peptides – Differential Scanning Fluorimetry and Hydrogen Deuterium Exchange Mass Spectrometry to Monitor the Conformational Dynamics of NBD1 in Cystic Fibrosis – A Multipronged Method for Unveiling Subtle Structural-Functional Defects of Mutant Chaperone Molecules Causing Human Chaperonopathies – High-Throughput Microplate-Based Fluorescence Assays for Studying Stochastic Aggregation of Superoxide Dismutase-1 – Methods for Structural Analysis of Amyloid Fibrils in Misfolding Diseases – Assays for Light Chain Amyloidosis Formation and Cytotoxicity – Monitoring Aggregate Clearance and Formation in Cell-Based Assays – Monitoring Proteome Stress in Live Cells Using HaloTag-Based Fluorogenic Sensor –