4.7 Article

Influence of Cortisol on the Fibril Formation Kinetics of Aβ42 Peptide: A Multi-Technical Approach

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MDPI
DOI: 10.3390/ijms23116007

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A beta 42 peptide; fibril formation; ThT fluorescence; secondary structure; infrared spectroscopy; atomic force microscopy; molecular dynamics

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  1. Progetti di Ricerca Ateneo Sapienza

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This paper presents a detailed analysis of in vitro A beta 42 fibril formation in the presence of cortisol and investigates its influence on the process. The research demonstrates that the concentration ratio of cortisol to A beta 42 plays a crucial role in promoting or inhibiting fibril formation.
Amyloid-beta peptide (A beta) aggregates are known to be correlated with pathological neurodegenerative diseases. The fibril formation process of such peptides in solution is influenced by several factors, such as the ionic strength of the buffer, concentration, pH, and presence of other molecules, just to mention a few. In this paper, we report a detailed analysis of in vitro A beta 42 fibril formation in the presence of cortisol at different relative concentrations. The thioflavin T fluorescence assay allowed us to monitor the fibril formation kinetics, while a morphological characterization of the aggregates was obtained by atomic force microscopy. Moreover, infrared absorption spectroscopy was exploited to investigate the secondary structure changes along the fibril formation path. Molecular dynamics calculations allowed us to understand the intermolecular interactions with cortisol. The combined results demonstrated the influence of cortisol on the fibril formation process: indeed, at cortisol-A beta 42 concentration ratio (rho) close to 0.1 a faster organization of A beta 42 fragments into fibrils is promoted, while for rho = 1 the formation of fibrils is completely inhibited.

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