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Molecular Targets in Protein Misfolding and Neurodegenerative Disease
- 1st Edition - October 7, 2014
- Author: Pierfausto Seneci
- Language: English
- Paperback ISBN:9 7 8 - 0 - 1 2 - 8 1 0 3 1 8 - 0
- Hardback ISBN:9 7 8 - 0 - 1 2 - 8 0 0 1 8 6 - 8
- eBook ISBN:9 7 8 - 0 - 1 2 - 8 0 0 4 9 9 - 9
Aimed at "drug discoverers" – i.e. any scientist who is interested in neurodegenerative diseases in general, and in finding disease-modifying treatments in particular – the fi… Read more
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Request a sales quoteAimed at "drug discoverers" – i.e. any scientist who is interested in neurodegenerative diseases in general, and in finding disease-modifying treatments in particular – the first edition of Molecular Targets in Protein Misfolding and Neurodegenerative Disease will contain both a detailed, discipline-specific coverage (paragraphs on medicinal chemistry, on clinical and preclinical characterization of compounds in development, on target identification and validation, on genetic factors influencing a pathology, etc.) and a drug discovery-oriented, overall evaluation of each target (validation, druggability, existing leads, etc.). Together these will satisfy the needs of various audiences, including in vitro biologists, pharmacologists, medicinal chemists, etc.
- Written to provide a comprehensive coverage of disease-modifying mechanisms and compounds against neurodegenerative diseases
- Provides a “drug discovery” application oriented perspective, evaluating targets and candidates for their overall therapeutic potential
- Provides discipline-specific chapters (medicinal chemistry, target validation, preclinical and clinical development
- Provides an overview on a number of molecular mechanisms (e.g. phosphorylation, chaperon refolding, ubiquitination, autophagy, microtubule transportation, protease cleavage, etc.) with relevance for any disease area
- Contains a more thorough description of the therapeutic relevance of ~10 specific molecular targets
Chapter 1: Protein Misfolding, Neurodegeneration and Tau
- Abstract
- 1.1. The neurodegeneration scenario
- 1.2. Protein folding: physiological benefits and pathological consequences
- 1.3. Tau: an intrinsically disordered, flexible, and aggregation-prone protein
- 1.4. Tauopathies: aggregation-prone tau in neurodegenerative disease (NDD)
Chapter 2: Targeting the Protein Quality Control (PQC) Machinery
- Abstract
- 2.1. Molecular chaperones, PQC, and neurodegeneration
- 2.2. Molecular targets
- 2.3. Disease-modifying compounds
Chapter 3: Proteasomal Degradation of Soluble, Misfolded Proteins
- Abstract
- 3.1. UPS-mediated degradation of misfolded proteins
- 3.2. UPS-mediated degradation of misfolded proteins in NDDs
- 3.3. UPS—targets
- 3.4. Disease-modifying compounds
Chapter 4: Unselective Disposal of Cellular Aggregates
- Abstract
- 4.1. Autophagy-mediated degradation of protein aggregates
- 4.2. Autophagy-mediated degradation of protein aggregates in NDDs
- 4.3. Macroautophagy—targets
- 4.4. Disease-modifying compounds
Chapter 5: Selective Disposal of Insoluble Protein Aggregates
- Abstract
- 5.1. Aggrephagy-mediated degradation of protein aggregates
- 5.2. Selective autophagy-mediated degradation of protein aggregates in NDDs
- 5.3. Selective autophagy—targets
- 5.4. Disease-modifying compounds
Chapter 6: Assembly and Disassembly of Protein Aggregates
- Abstract
- 6.1. Introduction
- 6.2. Disordered protein aggregates and ordered amyloid fibrils
- 6.3. Chaperone-driven disaggregation of protein aggregates
- 6.4. Disease-modifying compounds
- No. of pages: 314
- Language: English
- Edition: 1
- Published: October 7, 2014
- Imprint: Academic Press
- Paperback ISBN: 9780128103180
- Hardback ISBN: 9780128001868
- eBook ISBN: 9780128004999
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