Insights into the Assembly of Peptides Catalyzed by Polysaccharides

Nucleation is a critical step that determines the assembly pathway and the structure and functions of the peptide assemblies. However, the dynamic evolution of interactions between nucleating agents and peptides, as well as between peptides themselves during the nucleation process, remains elusive. Herein, we show that the heterogeneous nucleating agent carboxymethylcellulose (CMC) can promote the nucleation of Aβ<sub>16-20</sub> (KF) peptide. The Förster resonance energy transfer (FRET) technology was used to unveil the interaction dynamics between the CMC and KF peptide. Initially, CMC enriches KF monomers through weak nondirectional electrostatic interactions. The electrostatic screening reduces the electrostatic repulsion between KF molecules. Subsequently, KF-KF interactions become dominant, leading to the dissociation of KF from the CMC and nucleation. By adjustment of the adding time, dosage, size, and active sites of CMC, the assembly kinetics of KF can be effectively controlled. This study helps gain a deep understanding of the early heterogeneous nucleation process of peptide assembly and provides valuable guidance for the rational design of efficient nucleating agents for peptide assembly toward functional materials.

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Publication Details

Journal
The Journal of Physical Chemistry B
Published
2024-12-27
DOI
https://doi.org/10.1021/acs.jpcb.4c05751
Citations
1
Primary Topic
Supramolecular Self-Assembly in Materials
Type
article
Field-Weighted Citation Impact
0.17

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article

Insights into the Assembly of Peptides Catalyzed by Polysaccharides

Xiaoyu Cao, Yang Zhou, Zhong‐Qun Tian, Sheng He et al.
1 citations
The Journal of Physical Chemistry B
Supramolecular Self-Assembly in Materials
0.17
article

Insights into the Assembly of Peptides Catalyzed by Polysaccharides

Xiaoyu Cao, Yang Zhou, Zhong‐Qun Tian, Sheng He, Xinran Zhang, Wang Li, Liulin Yang
article en
1 citations

Abstract

Nucleation is a critical step that determines the assembly pathway and the structure and functions of the peptide assemblies. However, the dynamic evolution of interactions between nucleating agents and peptides, as well as between peptides themselves during the nucleation process, remains elusive. Herein, we show that the heterogeneous nucleating agent carboxymethylcellulose (CMC) can promote the nucleation of Aβ<sub>16-20</sub> (KF) peptide. The Förster resonance energy transfer (FRET) technology was used to unveil the interaction dynamics between the CMC and KF peptide. Initially, CMC enriches KF monomers through weak nondirectional electrostatic interactions. The electrostatic screening reduces the electrostatic repulsion between KF molecules. Subsequently, KF-KF interactions become dominant, leading to the dissociation of KF from the CMC and nucleation. By adjustment of the adding time, dosage, size, and active sites of CMC, the assembly kinetics of KF can be effectively controlled. This study helps gain a deep understanding of the early heterogeneous nucleation process of peptide assembly and provides valuable guidance for the rational design of efficient nucleating agents for peptide assembly toward functional materials.

The Journal of Physical Chemistry BVol. 129(1)
Xiamen University (CN), Collaborative Innovation Center of Chemistry for Energy Materials (CN)
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities, National Program for Support of Top-notch Young Professionals
Openalex Percentile: Top 48%
Supramolecular Self-Assembly in Materials
0.17
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Insights into the Assembly of Peptides Catalyzed by Polysaccharides — Xiaoyu Cao, Yang Zhou, et al. · The Journal of Physical Chemistry B (2024) | TGRS Research Map | TGRS