12. Neurotoxicity of Prion Peptides on Cultured Cerebellar Neurons
Giuseppe D. Ciccotosto, Metta Jana, and Roberto Cappai
PART III: Methods for Cell Free Propagation of Prions
13. Methods of Protein Misfolding Cyclic Amplification Natallia Makarava, Regina Savtchenko, and Ilia V. Baskakov
14. RT-QuIC Assays for Prion Disease Detection and Diagnostics
Christina D. Orrù, Bradley R. Groveman, Andrew G. Hughson, Matteo Manca, Lynne D. Raymond, Gregory J. Raymond, Katrina J. Campbell, Kelsie J. Anson, Allison Kraus, and Byron Caughey
15. A Quick Method to Evaluate the Effect of the Amino Acid Sequence in the Misfolding Proneness of the Prion Protein
16. Insights into Mechanisms of Transmission and Pathogenesis from Transgenic Mouse Models of Prion Diseases
Julie A. Moreno and Glenn C. Telling
17. In vivo Near Infrared Imaging of Neurodegeneration
Victoria A Lawson, Carolin Tumpach, Cathryn L Haigh, and Simon C Drew
18. Strain Typing of Prion Diseases using in vivo Mouse Models
Aileen Boyle, Kris Hogan, Jean C. Manson, and Abigail B Diack
19. Preparation and Immunostaining of the Myenteric Plexus of Prion Infected Mice
Laura J. Ellett and Victoria A. Lawson
PART V: Methods for the Detection and Treatment of Prion Diseases
20. Cell Culture Methods for Screening of Prion Therapeutics
Hilary E. McMahon
21. Real-Time Quaking Induced Conversion for Diagnosis of Prion Disease
Katsuya Satoh, Ryuichiro Atarashi, and Noriyuki Nishida
22. Methods for Molecular Diagnosis of Human Prion Disease
Jonathan D. F. Wadsworth, Gary Adamson, Susan Joiner, Lara Brock, Caroline Powell, Jacqueline M. Linehan, Jonathan A. Beck, Sebastian Brandner, Simon Mead, and John Collinge
23. Molecular sub-typing of PrPres in Human Sporadic CJD Brain Tissue
Klug, G.M., Lewis, V., and Collins, S.J.
Part VI: Methods for Investigation of Prion-like Disease
24. Intercellular Prion-like Conversion and Transmission of Cu/Zn Superoxide Dismutase (SOD1) in Cell Culture
Leslie I. Grad, Edward Pokrishevsky, and Neil R. Cashman
This volume details protocols on prion disease from multiple disciplines and highlights the contribution each discipline has made to the understanding of prion disease. Written in the highly successful Methods in Molecular Biology series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls.
Authoritative and practical, Prions: Methods and Protocols aims to ensure successful results in the further study of this vital field.