Physical principles of filamentous protein self-assembly kinetics. (13th March 2017)
- Record Type:
- Journal Article
- Title:
- Physical principles of filamentous protein self-assembly kinetics. (13th March 2017)
- Main Title:
- Physical principles of filamentous protein self-assembly kinetics
- Authors:
- Michaels, Thomas C T
Liu, Lucie X
Meisl, Georg
Knowles, Tuomas P J - Abstract:
- Abstract: The polymerization of proteins and peptides into filamentous supramolecular structures is an elementary form of self-organization of key importance to the functioning biological systems, as in the case of actin biofilaments that compose the cellular cytoskeleton. Aberrant filamentous protein self-assembly, however, is associated with undesired effects and severe clinical disorders, such as Alzheimer's and Parkinson's diseases, which, at the molecular level, are associated with the formation of certain forms of filamentous protein aggregates known as amyloids. Moreover, due to their unique physicochemical properties, protein filaments are finding extensive applications as biomaterials for nanotechnology. With all these different factors at play, the field of filamentous protein self-assembly has experienced tremendous activity in recent years. A key question in this area has been to elucidate the microscopic mechanisms through which filamentous aggregates emerge from dispersed proteins with the goal of uncovering the underlying physical principles. With the latest developments in the mathematical modeling of protein aggregation kinetics as well as the improvement of the available experimental techniques it is now possible to tackle many of these complex systems and carry out detailed analyses of the underlying microscopic steps involved in protein filament formation. In this paper, we review some classical and modern kinetic theories of protein filament formation,Abstract: The polymerization of proteins and peptides into filamentous supramolecular structures is an elementary form of self-organization of key importance to the functioning biological systems, as in the case of actin biofilaments that compose the cellular cytoskeleton. Aberrant filamentous protein self-assembly, however, is associated with undesired effects and severe clinical disorders, such as Alzheimer's and Parkinson's diseases, which, at the molecular level, are associated with the formation of certain forms of filamentous protein aggregates known as amyloids. Moreover, due to their unique physicochemical properties, protein filaments are finding extensive applications as biomaterials for nanotechnology. With all these different factors at play, the field of filamentous protein self-assembly has experienced tremendous activity in recent years. A key question in this area has been to elucidate the microscopic mechanisms through which filamentous aggregates emerge from dispersed proteins with the goal of uncovering the underlying physical principles. With the latest developments in the mathematical modeling of protein aggregation kinetics as well as the improvement of the available experimental techniques it is now possible to tackle many of these complex systems and carry out detailed analyses of the underlying microscopic steps involved in protein filament formation. In this paper, we review some classical and modern kinetic theories of protein filament formation, highlighting their use as a general strategy for quantifying the molecular-level mechanisms and transition states involved in these processes. … (more)
- Is Part Of:
- Journal of physics. Volume 29:Number 15(2017)
- Journal:
- Journal of physics
- Issue:
- Volume 29:Number 15(2017)
- Issue Display:
- Volume 29, Issue 15 (2017)
- Year:
- 2017
- Volume:
- 29
- Issue:
- 15
- Issue Sort Value:
- 2017-0029-0015-0000
- Page Start:
- Page End:
- Publication Date:
- 2017-03-13
- Subjects:
- amyloid -- nucleation -- mechanism -- self-assembly -- kinetics
Condensed matter -- Periodicals
Matière condensée -- Périodiques
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Natuurkunde
Electronic journals
Computer network resources
530.4105 - Journal URLs:
- http://www.iop.org/Journals/cm ↗
http://iopscience.iop.org/0953-8984/ ↗
http://ioppublishing.org/ ↗ - DOI:
- 10.1088/1361-648X/aa5f10 ↗
- Languages:
- English
- ISSNs:
- 0953-8984
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - BLDSS-3PM
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- 14503.xml