• In silico studies of the early stages of aggregation of Aβ₄₂ peptides

    • Fulltext

       

        Click here to view fulltext PDF


      Permanent link:
      https://www.ias.ac.in/article/fulltext/jcsc/129/07/0899-0909

    • Keywords

       

      Molecular simulation; intrinsically disordered protein; amyloid β.

    • Abstract

       

      Accumulation of amyloid beta (Aβ) peptide in the brain is responsible for debilitating neurodegenerative disease, namely, Alzheimer’s disease. We have carried out atomistic molecular dynamics simulation to study the early stages of the aggregation process of five full-length Aβ₄₂ peptide monomers with varying secondary structural contents in aqueous solution. Attempts have been made to study the conformational modifications of the Aβ peptide monomers and their dynamical features during the oligomer formation. Inparticular, specific molecular interactions that drive the association process leading to the formation of the stable oligomer have been identified. The calculations revealed that the helix–helix linkage plays an important role forbringing the unstructured regions of the monomers closer for self-assembly. Importantly, it is demonstrated that the contribution originating from the nonpolar interactions between the peptides and the corresponding nonpolarsolvation more than compensates the weakening effect of unfavorable inter-peptide electrostatic interactions, thereby stabilizing the nucleated oligomer.

    • Author Affiliations

       
    • Dates

       
  • Journal of Chemical Sciences | News

    • Editorial Note on Continuous Article Publication

      Posted on July 25, 2019

      Click here for Editorial Note on CAP Mode

© 2017-2019 Indian Academy of Sciences, Bengaluru.