Characterization and Optimization of Vesicle Properties in bioPISA: from Size Distribution to Post-Assembly Loading.

IF 3.2 3区 生物学 Q3 MATERIALS SCIENCE, BIOMATERIALS Advanced biology Pub Date : 2024-12-18 DOI:10.1002/adbi.202400483
Andrea Belluati, Adrian Bloch, Kaloian Koynov, Mariana Müller Nieva, Mohadeseh Bagherabadi, Annette Andrieu-Brunsen, Harald Kolmar, Nico Bruns
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引用次数: 0

Abstract

This study investigates the formation and properties of vesicles produced via biocatalytic Polymerization-Induced Self-Assembly (bioPISA) as artificial cells. Methods for achieving size uniformity, including gentle centrifugation and sucrose gradient centrifugation, are explored, and the effects of stirring speed on vesicle morphology is investigated. The internal structure of the vesicles, characterized by a polymer-rich matrix, is analyzed using fluorescence correlation spectroscopy (FCS). Additionally, the feasibility of loading macromolecules into pre-formed vesicles is demonstrated using electroporation, and a fluorescent protein as well as enzymes for a cascade reaction were sucesfully incorporated into the fully assembled polymersomes. These findings provide a foundation for developing enzyme-synthesized polymeric vesicles with controlled morphologies for various applications, e.g., in synthetic biology.

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生物 PISA 中囊泡特性的表征和优化:从粒度分布到组装后装载。
本研究研究了通过生物催化聚合诱导自组装(bioPISA)作为人工细胞产生的囊泡的形成和性质。探讨了实现粒径均匀的方法,包括温和离心和蔗糖梯度离心,并研究了搅拌速度对囊泡形态的影响。利用荧光相关光谱(FCS)分析了以富聚合物基质为特征的囊泡的内部结构。此外,利用电穿孔技术证明了将大分子装载到预先形成的囊泡中的可行性,并成功地将荧光蛋白和用于级联反应的酶结合到完全组装的聚合体中。这些发现为开发具有控制形态的酶合成聚合物囊泡的各种应用(例如在合成生物学中)提供了基础。
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来源期刊
Advanced biology
Advanced biology Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
6.60
自引率
0.00%
发文量
130
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