The Structure of Misfolded Amyloidogenic Dimers

Computational Analysis of Force Spectroscopy Data

Yuliang Zhang, Yuri L Lyubchenko

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

Progress in understanding the molecular mechanism of self-assembly of amyloidogenic proteins and peptides requires knowledge about their structure in misfolded states. Structural studies of amyloid aggregates formed during the early aggregation stage are very limited. Atomic force microscopy (AFM) spectroscopy is widely used to analyze misfolded proteins and peptides, but the structural characterization of transiently formed misfolded dimers is limited by the lack of computational approaches that allow direct comparison with AFM experiments. Steered molecular dynamics (SMD) simulation is capable of modeling force spectroscopy experiments, but the modeling requires pulling rates 107 times higher than those used in AFM experiments. In this study, we describe a computational all-atom Monte Carlo pulling (MCP) approach that enables us to model results at pulling rates comparable to those used in AFM pulling experiments. We tested the approach by modeling pulling experimental data for I91 from titin I-band (PDB ID: 1TIT) and ubiquitin (PDB ID: 1UBQ). We then used MCP to analyze AFM spectroscopy experiments that probed the interaction of the peptides [Q6C] Sup35 (6-13) and [H13C] Aβ (13-23). A comparison of experimental results with the computational data for the Sup35 dimer with out-of-register and in-register arrangements of β-sheets suggests that Sup35 monomers adopt an out-of-register arrangement in the dimer. A similar analysis performed for Aβ peptide demonstrates that the out-of-register antiparallel β-sheet arrangement of monomers also occurs in this peptide. Although the rupture of hydrogen bonds is the major contributor to dimer dissociation, the aromatic-aromatic interaction also contributes to the dimer rupture process.

Original languageEnglish (US)
Pages (from-to)2903-2910
Number of pages8
JournalBiophysical journal
Volume107
Issue number12
DOIs
StatePublished - Jan 1 2014

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Atomic Force Microscopy
Spectrum Analysis
Peptides
Rupture
Connectin
Amyloidogenic Proteins
Molecular Dynamics Simulation
Ubiquitin
Amyloid
Hydrogen
Proteins

ASJC Scopus subject areas

  • Biophysics

Cite this

The Structure of Misfolded Amyloidogenic Dimers : Computational Analysis of Force Spectroscopy Data. / Zhang, Yuliang; Lyubchenko, Yuri L.

In: Biophysical journal, Vol. 107, No. 12, 01.01.2014, p. 2903-2910.

Research output: Contribution to journalArticle

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