Analysis of the Growth Mechanism of Eumelanin Particles by Time-Resolved Static and Dynamic Light Scattering.

IF 5.5 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Biomacromolecules Pub Date : 2025-05-12 Epub Date: 2025-04-11 DOI:10.1021/acs.biomac.5c00158
Fabian Kollmann, Anne Büngeler, Miriam Splett, Oliver I Strube, Klaus Huber
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引用次数: 0

Abstract

Tyrosinase-catalyzed formation of eumelanin proceeds along four successive phases. The final phase is an aggregation of smaller type-A particles to larger type-B particles with a final radius of 200 nm. It is this fourth phase that is analyzed by means of time-resolved static and dynamic light scattering and UV-vis spectroscopy, providing the following significant insight into the formation mechanism of eumelanin. Growth of type-B particles requires a critical concentration of substrate l-Dopa. During an initial period of the reaction, disintegration of type-B particles is achieved with an appropriate increase of pH, demonstrating partial reversibility of the aggregation. Correlation of the size and mass of the growing type-B particles at variable pH levels and l-Dopa concentrations reveals that depending on the pH, the mechanism shifts from nucleation, followed by monomer addition, with type-A particles acting as the monomers, to a step growth process, where any two aggregates combine to form a corresponding larger aggregate.

真黑素颗粒生长机制的时间分辨静态和动态光散射分析。
酪氨酸酶催化的真黑素的形成沿着四个连续的阶段进行。最终阶段是由较小的a型颗粒向较大的b型颗粒聚集,最终半径为200nm。通过时间分辨静态和动态光散射以及紫外-可见光谱对这第四阶段进行了分析,为真黑色素的形成机制提供了以下重要见解。b型颗粒的生长需要一个临界浓度的底物左旋多巴。在反应的初始阶段,随着pH值的适当增加,b型颗粒实现了解体,表明聚集的部分可逆性。在不同的pH和l-Dopa浓度下,b型颗粒生长的大小和质量的相关性表明,随着pH的变化,机制从以a型颗粒为单体的成核后的单体加入转变为一个阶梯生长过程,其中任意两个聚集体结合形成相应的更大的聚集体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biomacromolecules
Biomacromolecules 化学-高分子科学
CiteScore
10.60
自引率
4.80%
发文量
417
审稿时长
1.6 months
期刊介绍: Biomacromolecules is a leading forum for the dissemination of cutting-edge research at the interface of polymer science and biology. Submissions to Biomacromolecules should contain strong elements of innovation in terms of macromolecular design, synthesis and characterization, or in the application of polymer materials to biology and medicine. Topics covered by Biomacromolecules include, but are not exclusively limited to: sustainable polymers, polymers based on natural and renewable resources, degradable polymers, polymer conjugates, polymeric drugs, polymers in biocatalysis, biomacromolecular assembly, biomimetic polymers, polymer-biomineral hybrids, biomimetic-polymer processing, polymer recycling, bioactive polymer surfaces, original polymer design for biomedical applications such as immunotherapy, drug delivery, gene delivery, antimicrobial applications, diagnostic imaging and biosensing, polymers in tissue engineering and regenerative medicine, polymeric scaffolds and hydrogels for cell culture and delivery.
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