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Selective ion-permeable membranes by insertion of biopores into polymersomes

机译:通过将生物孔插入聚合物囊泡中的选择性离子渗透膜

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摘要

In nature there are various specific reactions for which highly selective detection or support is required to preserve their bio-specificity or/and functionality. In this respect, mimics of cell membranes and bio-compartments are essential for developing tailored applications in therapeutic diagnostics. Being inspired by nature, we present here biomimetic nanocompartments with ion-selective membrane permeability engineered by insertion of ionomycin into polymersomes with sizes less than 250 nm. As a marker to assess the proper insertion and functionality of ionomycin inside the synthetic membrane, we used a Ca2+-sensitive dye encapsulated inside the polymersome cavity prior to inserting the biopore. The calcium sensitive dye, ionomycin, and Ca2+ did not influence the architecture and the size of polymersomes. Successful ionomycin functionality inside the synthetic membrane with a thickness of 10.7 nm was established by a combination of fluorescence spectroscopy and stopped-flow spectroscopy. Polymersomes equipped with ion selective membranes are ideal candidates for the development of medical applications, such as cellular ion nanosensors or nanoreactors in which ion exchange is required to support in situ reactions.
机译:实际上,存在各种特定的反应,需要对其进行高度选择性的检测或支持以保持其生物特异性或/和功能性。在这方面,细胞膜和生物隔室的模拟对于开发量身定制的治疗诊断学应用至关重要。受自然界的启发,我们在这里展示了通过将离子霉素插入尺寸小于250 nm的聚合物囊泡中而设计的具有离子选择性膜通透性的仿生纳米隔室。作为评估离子霉素在合成膜中正确插入和功能的标记,我们在插入生物孔之前使用了包裹在聚合物囊腔内部的Ca2 +敏感染料。钙敏感染料,离子霉素和Ca2 +不会影响多聚体的结构和大小。结合了荧光光谱和停止流光谱技术,成功建立了厚度为10.7 nm的合成膜内部成功的离子霉素功能。配备有离子选择性膜的聚合物囊泡是医疗应用开发的理想选择,例如需要离子交换以支持原位反应的细胞离子纳米传感器或纳米反应器。

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