Protein Misfolding Diseases : Methods and Protocols /

Detalles Bibliográficos
Autor Corporativo: SpringerLink (Online service)
Otros Autores: Gomes, Cláudio M. (Editor )
Formato: eBook
Lenguaje:English
Publicado: New York, NY : Springer New York : Imprint: Humana, 2019.
Edición:1st ed. 2019.
Colección:Methods in Molecular Biology, 1873
Materias:
Tabla de Contenidos:
  • 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
  • Quantification of Protein Aggregates Using Bimolecular Fluorescence Complementation
  • Screening Protein Aggregation in Cells Using Fluorescent Labels Coupled to Flow Cytometry
  • Induction of Cu/Zn Superoxide Dismutase (SOD1) Aggregation in Living Cells
  • A Cell Model for HSP60 Deficiencies: Modeling Different Levels of Chaperonopathies Leading to Oxidative Stress and Mitochondrial Dysfunction
  • Super-Resolution Fluorescence Imaging of Mutant Huntingtin Aggregation in Cells
  • Thermal Shift and Stability Assays of Disease-Related Misfolded Proteins Using Differential Scanning Fluorimetry
  • Methods to Screen Compounds against Mutant p53 Misfolding and Aggregation for Cancer Therapeutics
  • Early Stage Discovery and Validation of Pharmacological Chaperones for the Correction of Protein Misfolding Diseases
  • Constructing Kinetically Controlled Denaturation Isotherms of Folded Proteins Using Denaturant-Pulse Chaperonin Binding
  • In Vitro Prion Amplification Methodology for Inhibitor Screening
  • SolubiS: Optimizing Protein Solubility by Minimal Point Mutations.