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多酶响应型聚合物制剂的级联中间相转变。

Cascade Mesophase Transitions of Multi-enzyme Responsive Polymeric Formulations.

机构信息

School of Chemistry, Faculty of Exact Sciences, Tel-Aviv University, Tel-Aviv 6997801, Israel.

The Center for Physics and Chemistry of Living Systems, Tel-Aviv University, Tel Aviv 6997801, Israel.

出版信息

Biomacromolecules. 2024 Jun 10;25(6):3607-3619. doi: 10.1021/acs.biomac.4c00221. Epub 2024 May 22.

Abstract

Studying how synthetic polymer assemblies respond to sequential enzymatic stimuli can uncover intricate interactions in biological systems. Using amidase- and esterase-responsive PEG-based diblock (DBA) and triblock amphiphiles (TBAs), we created two distinct formulations: amidase-responsive DBA with esterase-responsive TBA and vice versa. We studied their cascade responses to the two enzymes and the sequence of their introduction. These formulations underwent cascade mesophase transitions upon the addition of the DBA-degrading enzyme, transitioning from (i) coassembled micelles to (ii) triblock-based hydrogel, and ultimately to (iii) dissolved polymers when exposed to the TBA hydrolyzing enzyme. The specific pathway of the two mesophase transitions depended on the compositions of the formulations and the enzyme introduction sequence. The results highlight the potential for designing polymeric formulations with programmable multistep enzymatic responses, mimicking the complex behavior of biological macromolecules.

摘要

研究合成聚合物组装体如何响应顺序酶刺激,可以揭示生物系统中的复杂相互作用。使用酰胺酶和酯酶响应的 PEG 基二嵌段(DBA)和三嵌段两亲物(TBA),我们创建了两种不同的配方:酰胺酶响应的 DBA 和酯酶响应的 TBA,反之亦然。我们研究了它们对两种酶的级联反应以及它们引入的顺序。当加入 DBA 降解酶时,这些配方经历级联中间相转变,从(i)共组装胶束转变为(ii)基于三嵌段的水凝胶,最终在暴露于 TBA 水解酶时转变为(iii)溶解聚合物。两种中间相转变的特定途径取决于配方的组成和酶引入顺序。结果强调了设计具有可编程多步酶反应的聚合物配方的潜力,模拟生物大分子的复杂行为。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5a9/11170936/c4700f1d4845/bm4c00221_0006.jpg

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