Role of Proteases in the Pathophysiology of Neurodegenerative Diseases:
Researchers seeking problems that offer more hope of success often avoid subjects that seem to be difficult to approach experimentally, or subjects for which experimental results are difficult to interpret. The breakdown part of protein turnover in vivo, particularly in nervous tissue, was such a su...
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Weitere Verfasser: | , |
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Format: | Elektronisch E-Book |
Sprache: | English |
Veröffentlicht: |
Boston, MA
Springer US
2002
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Schlagworte: | |
Online-Zugang: | DE-355 Volltext |
Zusammenfassung: | Researchers seeking problems that offer more hope of success often avoid subjects that seem to be difficult to approach experimentally, or subjects for which experimental results are difficult to interpret. The breakdown part of protein turnover in vivo, particularly in nervous tissue, was such a subject in the past – it was difficult to measure and difficult to explore the mechanisms involved. For factors that influence protein metabolism, it was thought that protein content, function, and distribution are controlled only by the synthetic mechanisms that can supply the needed specificity and response to stimuli. The role of breakdown was thought to be only a general metabolic digestion, elimination of excess polypeptides. We now know that the role of breakdown is much more complex: it has multiple functions, it is coupled to turnover, and it can affect protein composition, function, and synthesis. In addition to eliminating abnormal proteins, breakdown has many modulatory functions: it serves to activate and inactivate enzymes, modulate membrane function, alter receptor channel properties, affect transcription and cell cycle, form active peptides, and much more. The hydrolysis of peptide bonds often involves multiple steps, many enzymes, and cycles (such as ubiquination), and often requires the activity of enzyme complexes. Their activation, modification, and inactivation can thus play an important role in biological functions, with numerous families of proteases participating. The specific role of each remains to be elucidated |
Beschreibung: | 1 Online-Ressource (XIV, 302 p) |
ISBN: | 9780306468476 |
DOI: | 10.1007/b111075 |
Internformat
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Datensatz im Suchindex
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discipline | Medizin |
doi_str_mv | 10.1007/b111075 |
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isbn | 9780306468476 |
language | English |
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spelling | Role of Proteases in the Pathophysiology of Neurodegenerative Diseases edited by Abel Lajtha, Naren L. Banik Boston, MA Springer US 2002 1 Online-Ressource (XIV, 302 p) txt rdacontent c rdamedia cr rdacarrier Researchers seeking problems that offer more hope of success often avoid subjects that seem to be difficult to approach experimentally, or subjects for which experimental results are difficult to interpret. The breakdown part of protein turnover in vivo, particularly in nervous tissue, was such a subject in the past – it was difficult to measure and difficult to explore the mechanisms involved. For factors that influence protein metabolism, it was thought that protein content, function, and distribution are controlled only by the synthetic mechanisms that can supply the needed specificity and response to stimuli. The role of breakdown was thought to be only a general metabolic digestion, elimination of excess polypeptides. We now know that the role of breakdown is much more complex: it has multiple functions, it is coupled to turnover, and it can affect protein composition, function, and synthesis. In addition to eliminating abnormal proteins, breakdown has many modulatory functions: it serves to activate and inactivate enzymes, modulate membrane function, alter receptor channel properties, affect transcription and cell cycle, form active peptides, and much more. The hydrolysis of peptide bonds often involves multiple steps, many enzymes, and cycles (such as ubiquination), and often requires the activity of enzyme complexes. Their activation, modification, and inactivation can thus play an important role in biological functions, with numerous families of proteases participating. The specific role of each remains to be elucidated Neurosciences Neurology Proteasen (DE-588)4047521-9 gnd rswk-swf Pathophysiologie (DE-588)4044898-8 gnd rswk-swf Nervendegeneration (DE-588)4300182-8 gnd rswk-swf Nervendegeneration (DE-588)4300182-8 s Pathophysiologie (DE-588)4044898-8 s Proteasen (DE-588)4047521-9 s 1\p DE-604 Lajtha, Abel edt Banik, Naren L. edt Erscheint auch als Druck-Ausgabe 9781441933607 Erscheint auch als Druck-Ausgabe 9780306465796 Erscheint auch als Druck-Ausgabe 9781475786965 https://doi.org/10.1007/b111075 Verlag URL des Erstveröffentlichers Volltext 1\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk |
spellingShingle | Role of Proteases in the Pathophysiology of Neurodegenerative Diseases Neurosciences Neurology Proteasen (DE-588)4047521-9 gnd Pathophysiologie (DE-588)4044898-8 gnd Nervendegeneration (DE-588)4300182-8 gnd |
subject_GND | (DE-588)4047521-9 (DE-588)4044898-8 (DE-588)4300182-8 |
title | Role of Proteases in the Pathophysiology of Neurodegenerative Diseases |
title_auth | Role of Proteases in the Pathophysiology of Neurodegenerative Diseases |
title_exact_search | Role of Proteases in the Pathophysiology of Neurodegenerative Diseases |
title_full | Role of Proteases in the Pathophysiology of Neurodegenerative Diseases edited by Abel Lajtha, Naren L. Banik |
title_fullStr | Role of Proteases in the Pathophysiology of Neurodegenerative Diseases edited by Abel Lajtha, Naren L. Banik |
title_full_unstemmed | Role of Proteases in the Pathophysiology of Neurodegenerative Diseases edited by Abel Lajtha, Naren L. Banik |
title_short | Role of Proteases in the Pathophysiology of Neurodegenerative Diseases |
title_sort | role of proteases in the pathophysiology of neurodegenerative diseases |
topic | Neurosciences Neurology Proteasen (DE-588)4047521-9 gnd Pathophysiologie (DE-588)4044898-8 gnd Nervendegeneration (DE-588)4300182-8 gnd |
topic_facet | Neurosciences Neurology Proteasen Pathophysiologie Nervendegeneration |
url | https://doi.org/10.1007/b111075 |
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