冷冻电镜揭示两性多肽自组装过程中的关键中间纳米结构

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Yen Jea Lee, Xubo Luo, Morgan Seidler, Tianyi Yu, David Prendergast, Ronald N. Zuckermann, Nitash P. Balsara, Brooks A. Abel, Xi Jiang
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引用次数: 0

摘要

已知两亲性共聚肽类可以形成各种纳米结构(纤维、管、片等),但其组装机制和关键中间体仍未得到充分研究。本研究利用低温透射电镜(cryo-TEM)研究了二嵌段共聚物类肽自组装早期形成的中间结构。我们重点研究了两种二嵌段共聚肽,一种具有自由的n端,另一种具有带帽的n端,它们最终分别形成了有序的纳米纤维和有序的纳米片。通过对玻璃化溶液在自组装过程中不同时间点的低温透射电镜成像,研究确定了胶束和囊泡是关键的中间结构。值得注意的是,在结晶驱动的自组装中,囊泡作为中间体的形成是不寻常的,这表明多肽自组装有一种独特的途径。该研究为多肽自组装的关键中间体提供了直接的成像证据,促进了对其自组装机制的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Key Intermediate Nanostructures in the Self-Assembly of Amphiphilic Polypeptoids Revealed by Cryo-TEM

Key Intermediate Nanostructures in the Self-Assembly of Amphiphilic Polypeptoids Revealed by Cryo-TEM
Amphiphilic copolypeptoids are known to form a variety of nanostructures (fibers, tubes, sheets, etc.), but the assembly mechanisms and key intermediates remain underexplored. This study investigates the intermediate structures formed during the early stages of self-assembly in diblock copolypeptoids using cryo-transmission electron microscopy (cryo-TEM). We focused on two diblock copolypeptoids, one with a free N-terminus and the other with a capped N-terminus, which ultimately form less-ordered nanofibers and well-ordered nanosheets, respectively. Through cryo-TEM imaging of vitrified solutions at various time points during the self-assembly process, the study identified micelles and vesicles as key intermediate structures. Notably, the formation of vesicles as intermediates is unusual in crystallization-driven self-assembly and suggests a unique pathway in polypeptoid self-assembly. The study provides direct imaging evidence of key intermediates in polypeptoid self-assembly, advancing the understanding of their self-assembly mechanisms.
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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