@article {716,
	title = {Evidence for the existence of a secondary pathway for fibril growth during the aggregation of tau.},
	journal = {J Mol Biol},
	volume = {421},
	year = {2012},
	month = {2012 Aug 10},
	pages = {296-314},
	abstract = {<p>The mechanism of amyloid fibril formation by proteins has been classically described by the nucleation-dependent polymerization (NDP) model, which makes certain predictions regarding the kinetics of fibrillation. All proteins whose aggregation conforms to the NDP model display a t(2) time dependence for their initial reaction profile. However, there are proteins whose aggregation reactions have kinetic signatures of a flat lag phase followed by an exponential rise in fibril mass, which does not conform to the NDP model. Amyloid fibril formation by tau, a microtubule-associated protein whose aggregation to form neurofibrillary tangles is implicated in Alzheimer{\textquoteright}s disease and other tauopathies, in the presence of inducers such as heparin and fatty acid micelles, has always been traditionally described by a ligand-induced NDP model. In this study, the existence of a secondary pathway for fibril growth during the aggregation of the functional, repeat domain of tau in the presence of heparin has been established. Both kinetic and accessory evidence are provided for the existence of this pathway, which is shown to augment the primary homogeneous nucleation pathway. From the kinetic data, the main secondary pathway that is operative appears to be fibril fragmentation but other pathways such as branching or secondary nucleation may also be operative.</p>
},
	keywords = {Amyloid, Kinetics, Micelles, Microscopy, Atomic Force, Models, Chemical, tau Proteins},
	issn = {1089-8638},
	doi = {10.1016/j.jmb.2012.01.007},
	author = {Ramachandran, Gayathri and Udgaonkar, Jayant B}
}
