Thermodynamic description of Beta amyloid formation using physicochemical scales and fractal bioinformatic scales.

Abstract:

:Protein function depends on both protein structure and amino acid (aa) sequence. Here we show that modular features of both structure and function can be quantified economically from the aa sequences alone for the small (40,42 aa) plaque-forming (aggregative) amyloid beta fragments. Some edge and center features of the fragments are predicted. Bioinformatic scales based on β strand formation propensities and the thermodynamically second order fractal hydropathicity scale based on evolutionary optimization (self-organized criticality) are contrasted with the standard first order physicochemical scale based on complete protein (water-air) unfolding. The results are consistent with previous studies of these physicochemical factors that show that aggregative properties, even of beta fragments, are driven primarily by near-equilibrium hydropathic forces.

journal_name

ACS Chem Neurosci

authors

Phillips JC

doi

10.1021/cn5001793

subject

Has Abstract

pub_date

2015-05-20 00:00:00

pages

745-50

issue

5

issn

1948-7193

journal_volume

6

pub_type

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