Issue 21, 2023

An amphiphilic material arginine–arginine–bile acid promotes α-synuclein amyloid formation

Abstract

Amyloid generation plays essential roles in various human diseases, biological functions, and nanotechnology. However, developing efficient chemical and biological candidates for regulating amyloid fibrillation remains difficult because information on the molecular actions of modulators is insufficient. Thus, studies are needed to understand how the intermolecular physicochemical properties of the synthesised molecules and amyloid precursors influence amyloidogenesis. In this study, we synthesised a novel amphiphilic sub-nanosized material, arginine–arginine (RR)–bile acid (BA), by conjugating positively charged RR to hydrophobic BA. The effects of RR–BA on amyloid formation were investigated on α-synuclein (αSN) in Parkinson's disease and on K18 and amyloid-β (1–42) (Aβ42) in Alzheimer's disease. RR–BA showed no appreciable effect on the kinetics of K18 and Aβ42 amyloid fibrillation because of their weak and non-specific interactions. However, RR–BA specifically bound to αSN with moderate binding affinity through electrostatic interactions between the positively charged RR and the negatively charged cluster in the C-terminus of αSN. In addition, hydrophobic BA in the αSN–RR–BA complex transiently condensed αSN for primary nucleation, thereby accelerating αSN amyloid fibrillation. We propose an electrostatic binding and hydrophobic condensation model of RR–BA-driven amyloid formation of αSN, which will contribute to the rational design and development of molecules for controlling amyloid aggregation in diverse fields.

Graphical abstract: An amphiphilic material arginine–arginine–bile acid promotes α-synuclein amyloid formation

Supplementary files

Article information

Article type
Paper
Submitted
29 mar. 2023
Accepted
10 apr. 2023
First published
09 maí 2023

Nanoscale, 2023,15, 9315-9328

An amphiphilic material arginine–arginine–bile acid promotes α-synuclein amyloid formation

Y. Lin, S. Park, E. Bok, Y. Heo, S. Yang, Y. Yi, J. Lee, D. Seo, E. Jo, S. Lim, Y. K. Kim, J. Kardos, K. Ryu, J. Kim, J. Park and Y. Lee, Nanoscale, 2023, 15, 9315 DOI: 10.1039/D3NR01468A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements