A lattice Monte Carlo model for amyloid fibril formation.

Authors

Hisashi Okumura, Linh Truong Hoai, Pornthep Sompornpisut, Satoru G Itoh

Published in

Biophysics and physicobiology. Volume 23. Issue 2. Pages e230015. Epub May 09, 2026.

Abstract

Proteins can aggregate to form amyloid fibrils, which are associated with a group of diseases collectively known as amyloidoses. Molecular dynamics simulations are widely used to study protein aggregation; however, it remains computationally challenging to investigate the entire aggregation process, from initial nucleation to the formation of mature amyloid fibrils, within a single simulation. In this study, we propose a Monte Carlo simulation based on a mathematical lattice model in which proteins are represented as spheres on a lattice. Motivated by the role of intramolecular β-sheet structures in accelerating aggregation, we classify protein states into three categories: monomer, intermediate possessing an intramolecular β-sheet structure, and fibril. By tuning the monomer-to-intermediate transition probability P _MI and the intermediate-to-fibril transition probability P _IF, both kinetics and morphology of amyloid fibril formation can be systematically controlled. When P _MI is low, a lag time appears in the early stage of aggregation, whereas increasing P _MI shortens the lag time. High values of both P _MI and P _IF lead to rapid aggregation and the formation of many short fibrils, while low values result in slower aggregation and fewer but longer fibrils. These results are consistent with experimental observations and indicate that amyloid fibril formation can be understood as a crystal growth process. This approach is expected to provide further insight into the universal mechanisms of amyloid fibril formation in homogeneous aqueous environments, as well as in heterogeneous and nonequilibrium systems.

PMID:
42371580
Bibliographic data and abstract were imported from PubMed on 29 Jun 2026.

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