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Role of Proteases in the Pathophysiology of Neurodegenerative Diseases (Hardcover, 2001 ed.)
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Role of Proteases in the Pathophysiology of Neurodegenerative Diseases (Hardcover, 2001 ed.)
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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.
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