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Supramolecular cellular filament systems: How and why do they form?

Journal

CYTOSKELETON
Volume 69, Issue 2, Pages 71-87

Publisher

WILEY
DOI: 10.1002/cm.21006

Keywords

cellular filament systems; molecular crowding; cation counterion fluctuations; liquid crystals; supramolecular structures

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Funding

  1. Agency for Science, Technology and Research (A*STAR), Singapore
  2. Joint Council Office (JCO) [10/03/FG/06/04]
  3. ERATO, JST, Japan

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All cells, from simple bacteria to complex human tissues, rely on extensive networks of protein fibers to help maintain their proper form and function. These filament systems usually do not operate as single filaments, but form complex suprastructures, which are essential for specific cellular functions. Here, we describe the progress in determining the architectures of molecular filamentous suprastructures, the principles leading to their formation, and the mechanisms by which they may facilitate function. The complex eukaryotic cytoskeleton is tightly regulated by a large number of actin- or microtubule-associated proteins. In contrast, recently discovered bacterial actins and tubulins have few associated regulatory proteins. Hence, the quest to find basic principles that govern the formation of filamentous suprastructures is simplified in bacteria. Three common principles, which have been probed extensively during evolution, can be identified that lead to suprastructures formation: cationic counterion fluctuations; self-association into liquid crystals; and molecular crowding. The underlying physics of these processes will be discussed with respect to physiological circumstance. (c) 2012 Wiley Periodicals, Inc

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