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Biophys. J. BioFAST: First Published September 21, 2007. doi:10.1529/biophysj.107.117168
© 2007 by the Biophysical Society.


A more recent version of this article appeared on January 15, 2008.
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BIOPHYSICAL THEORY AND MODELING

Mechanisms of Protein Fibril Formation: Nucleated Polymerization with Competing Off-Pathway Aggregation

Evan T Powers 1* and David L Powers 2

1 The Scripps Research Institute
2 Clarkson University

* To whom correspondence should be addressed. E-mail: epowers{at}scripps.edu.

Submitted on July 10, 2007
Revised on August 14, 2007
Accepted on 7 September 2007


   Abstract
The formation of protein fibrils, and in particular amyloid fibrils, underlies many human diseases. Understanding fibril formation mechanisms is important for understanding disease pathology, but fibril formation kinetics can be complicated, making the relationship between experimental observables and specific mechanisms unclear. Here we examine one often-proposed fibril formation mechanism, nucleated polymerization with off-pathway aggregation. We use the characteristics of this mechanism to derive three tests that can be performed on experimental data to identify it. We also find that this mechanism has an especially striking feature: while increasing protein concentrations generally cause simple nucleated polymerizations to reach completion faster, they cause nucleated polymerizations with off-pathway aggregation to reach completion more slowly when the protein concentration becomes too high.

Key Words: aggregation, amyloid, kinetics, mechanism, protein fibril







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Copyright © 2007 by the Biophysical Society.