5 years ago

Simple Model of the Effect of Solution Conditions on the Nucleation of Amyloid Fibrils

Simple Model of the Effect of Solution Conditions on the Nucleation of Amyloid Fibrils
Stefan Auer
It is well known that peptide and protein fibrillation is strongly affected by the solution conditions, but a fundamental understanding of how amyloid fibril nucleation depends on solution pH, salt concentration, and solvent is absent. Here, we use expressions from Debye–Hückel theory to describe the interactions between charged amino acids in combination with our recently developed nonstandard nucleation theory to predict the concentration dependence of the fibril nucleation rate under different solvent conditions. The general rule that emerges from these considerations is that changes in solution pH, salt concentration, and solvent that increase the bonding energy between the fibril building blocks decrease the fibril solubility and promote fibril nucleation, in line with experimental observations. The simple analytical relations among the nucleation rate, fibril solubility, and binding energies provide a tool to controlling and understanding amyloid fibril formation by changing the solution conditions.

Publisher URL: http://dx.doi.org/10.1021/acs.jpcb.7b05400

DOI: 10.1021/acs.jpcb.7b05400

You might also like
Discover & Discuss Important Research

Keeping up-to-date with research can feel impossible, with papers being published faster than you'll ever be able to read them. That's where Researcher comes in: we're simplifying discovery and making important discussions happen. With over 19,000 sources, including peer-reviewed journals, preprints, blogs, universities, podcasts and Live events across 10 research areas, you'll never miss what's important to you. It's like social media, but better. Oh, and we should mention - it's free.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.