Literature DB >> 14967245

Effects of inert volume-excluding macromolecules on protein fiber formation. II. Kinetic models for nucleated fiber growth.

Damien Hall1, Allen P Minton.   

Abstract

A sequential model for nucleated protein fiber formation is proposed that is similar in broad outline to models proposed previously (Thermodynamics of the Polymerization of Protein, Academic Press, New York, (1975); Biophys. J. 50 (1986) 583) but generalized to allow for thermodynamic nonideality resulting from a high degree of volume occupancy by inert macromolecular cosolutes (macromolecular crowding). The effect of volume occupancy on the rate of fiber formation is studied in the transition-state rate-limited regime through systematic variation of rate-limiting step (prenuclear oligomer formation, nucleus formation or fiber growth), shape of prenuclear oligomer, size of nucleus, extent of reversibility, nature of inert cosolute (hard globular particle or random coil polymer) and size of inert cosolute relative to that of fiber-forming protein. It is found that crowding can accelerate the rate of fiber formation by as much as several orders of magnitude. The extent of acceleration for a given degree of volume occupancy depends upon several factors, the most conspicuous of which is the stoichiometry of the nucleus. In contrast, the rate of redistribution of fiber length, which occurs on a much slower time scale than polymer formation, is found to be insensitive to the extent of crowding.

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Year:  2004        PMID: 14967245     DOI: 10.1016/j.bpc.2003.09.016

Source DB:  PubMed          Journal:  Biophys Chem        ISSN: 0301-4622            Impact factor:   2.352


  9 in total

1.  Protein self-association in the cell: a mechanism for fine tuning the level of macromolecular crowding?

Authors:  Damien Hall
Journal:  Eur Biophys J       Date:  2005-10-11       Impact factor: 1.733

2.  Coarse-grained strategy for modeling protein stability in concentrated solutions.

Authors:  Jason K Cheung; Thomas M Truskett
Journal:  Biophys J       Date:  2005-07-22       Impact factor: 4.033

3.  Entropy-driven genome organization.

Authors:  Davide Marenduzzo; Cristian Micheletti; Peter R Cook
Journal:  Biophys J       Date:  2006-02-24       Impact factor: 4.033

4.  Energetics and geometry of FtsZ polymers: nucleated self-assembly of single protofilaments.

Authors:  Sonia Huecas; Oscar Llorca; Jasminka Boskovic; Jaime Martín-Benito; José María Valpuesta; José Manuel Andreu
Journal:  Biophys J       Date:  2007-11-16       Impact factor: 4.033

5.  A multi-pathway perspective on protein aggregation: implications for control of the rate and extent of amyloid formation.

Authors:  Damien Hall; József Kardos; Herman Edskes; John A Carver; Yuji Goto
Journal:  FEBS Lett       Date:  2015-01-31       Impact factor: 4.124

6.  Parameter effects on binding chemistry in crowded media using a two-dimensional stochastic off-lattice model.

Authors:  Byoungkoo Lee; Philip R LeDuc; Russell Schwartz
Journal:  Phys Rev E Stat Nonlin Soft Matter Phys       Date:  2009-10-14

7.  Computational modeling of the relationship between amyloid and disease.

Authors:  Damien Hall; Herman Edskes
Journal:  Biophys Rev       Date:  2012-09

8.  On the nature of the optimal form of the holdase-type chaperone stress response.

Authors:  Damien Hall
Journal:  FEBS Lett       Date:  2019-09-21       Impact factor: 3.864

Review 9.  Measurement of amyloid formation by turbidity assay-seeing through the cloud.

Authors:  Ran Zhao; Masatomo So; Hendrik Maat; Nicholas J Ray; Fumio Arisaka; Yuji Goto; John A Carver; Damien Hall
Journal:  Biophys Rev       Date:  2016-11-23
  9 in total

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