Amyloid oligomers: A joint experimental/computational perspective on Alzheimer's disease, Parkinson's disease, type II diabetes, and amyotrophic lateral sclerosis

PH Nguyen, A Ramamoorthy, BR Sahoo… - Chemical …, 2021 - ACS Publications
Protein misfolding and aggregation is observed in many amyloidogenic diseases affecting
either the central nervous system or a variety of peripheral tissues. Structural and dynamic …

Characterization of lipid–protein interactions and lipid-mediated modulation of membrane protein function through molecular simulation

MP Muller, T Jiang, C Sun, M Lihan, S Pant… - Chemical …, 2019 - ACS Publications
The cellular membrane constitutes one of the most fundamental compartments of a living
cell, where key processes such as selective transport of material and exchange of …

Computer simulations of protein–membrane systems

J Loschwitz, OO Olubiyi, JS Hub, B Strodel… - Progress in molecular …, 2020 - Elsevier
The interactions between proteins and membranes play critical roles in signal transduction,
cell motility, and transport, and they are involved in many types of diseases. Molecular …

[HTML][HTML] Molecular mechanisms of membrane-associated amyloid aggregation: Computational perspective and challenges

O Press-Sandler, Y Miller - Biochimica et Biophysica Acta (BBA) …, 2018 - Elsevier
Amyloidogenic proteins are related to a variety of amyloid diseases, such as type 2 diabetes
(T2D), Alzheimer's disease (AD) and Parkinson's disease (PD). The amyloid proteins in …

[HTML][HTML] Recent computational studies of membrane interaction and disruption of human islet amyloid polypeptide: Monomers, oligomers and protofibrils

X Dong, Q Qiao, Z Qian, G Wei - Biochimica et Biophysica Acta (BBA) …, 2018 - Elsevier
The amyloid deposits of human islet amyloid polypeptide (hIAPP) are found in type 2
diabetes patients. hIAPP monomer is intrinsically disordered in solution, whereas it can form …

Interplay between membrane composition and structural stability of membrane-bound hIAPP

GL Dignon, GH Zerze, J Mittal - The Journal of Physical Chemistry …, 2017 - ACS Publications
Amyloid aggregates are characteristic of many serious diseases such as Alzheimer's
disease, Parkinson's, and type 2 diabetes and commonly involve intrinsically disordered …

Molecular Insights into Distinct Membrane-insertion Behaviors and Mechanisms of 20 Amino Acids: an All-atom MD Simulation Study

W Tu, X Dong, L Ou, X Zhang, B Yuan… - Chemical Research in …, 2023 - Springer
I nterfacial interactions of proteins with cell membranes play important roles in fundamental
physiological processes of cells. The binding of proteins to membranes involves interactions …

Molecular basis of the anchoring and stabilization of human islet amyloid polypeptide in lipid hydroperoxidized bilayers

YR Espinosa, DIB Valderrama, CM Carlevaro… - … et Biophysica Acta (BBA …, 2022 - Elsevier
The molecular structure of membrane lipids is formed by mono-or polyunsaturations on their
aliphatic tails that make them susceptible to oxidation, facilitating the incorporation of …

Coexisting Ordered and Disordered Membrane Phases Have Distinct Modes of Interaction with Disease-Associated Oligomers

A Gupta, S Dey, D Bhowmik, S Maiti - The Journal of Physical …, 2022 - ACS Publications
Ordered membrane domains are thought to influence the attachment and insertion of toxic
amyloid oligomers, and consequently, their toxicity. However, if and how the molecular …

Formation of α-helical and β-sheet Structures in Membrane-Bound Human IAPP Monomer and the Resulting Membrane Deformation

Q Qiao, G Wei, D Yao, Z Song - Physical Chemistry Chemical Physics, 2019 - pubs.rsc.org
The amyloid formation of human islet amyloid polypeptide (hIAPP)—an intrinsically
disordered peptide, is associated with type II diabetes. Cellular membranes, especially …