Fabricating SilverNanoparticles with Antidiabetic d‑Pinitol to RestrictAmyloid Formation of Insulin

In this study, we synthesized silver nanoparticles functionalized with antidiabetic d-pinitol molecules and investigated their anti-amyloid effect on Insulin aggregation. Our results show that these functionalized nanoparticles effectively inhibit both spontaneous and seed-induced amyloid aggregation of Insulin in a dose-dependent manner. The d-pinitol-functionalized silver nanoparticles interact directly with the aggregation-prone regions of Insulin’s partially unfolded structures, as demonstrated by quenching and computational experiments. Analysis of docking and simulation data suggests that antiamyloid activity of d-pinitol functionalized AgNPs is due to a strong Insulin-nanoparticle interaction, facilitated via hydrogen bonds. These interactions disrupt the Insulin monomer–dimer equilibrium and prevent the formation of toxic amyloid structures. The results could lead to the development of d-pinitol-based Insulin-stabilizing nanoformulations with potential antidiabetic properties.

Publication Details

Journal
Figshare
Published
2025-02-10
DOI
https://doi.org/10.1021/acsabm.4c01224.s001
Primary Topic
Genetic and Environmental Crop Studies
Type
article
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article

Fabricating SilverNanoparticles with Antidiabetic d‑Pinitol to RestrictAmyloid Formation of Insulin

Figshare
Genetic and Environmental Crop Studies
article

Fabricating SilverNanoparticles with Antidiabetic d‑Pinitol to RestrictAmyloid Formation of Insulin

article en

Abstract

In this study, we synthesized silver nanoparticles functionalized with antidiabetic d-pinitol molecules and investigated their anti-amyloid effect on Insulin aggregation. Our results show that these functionalized nanoparticles effectively inhibit both spontaneous and seed-induced amyloid aggregation of Insulin in a dose-dependent manner. The d-pinitol-functionalized silver nanoparticles interact directly with the aggregation-prone regions of Insulin’s partially unfolded structures, as demonstrated by quenching and computational experiments. Analysis of docking and simulation data suggests that antiamyloid activity of d-pinitol functionalized AgNPs is due to a strong Insulin-nanoparticle interaction, facilitated via hydrogen bonds. These interactions disrupt the Insulin monomer–dimer equilibrium and prevent the formation of toxic amyloid structures. The results could lead to the development of d-pinitol-based Insulin-stabilizing nanoformulations with potential antidiabetic properties.

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Openalex Percentile: Top 40%
Genetic and Environmental Crop Studies
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