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电荷密度作为无序蛋白聚合物纳米结构化的分子调节剂。

Charge Density as a Molecular Modulator of Nanostructuration in Intrinsically Disordered Protein Polymers.

机构信息

Bioforge Lab, CIBER-BBN, University of Valladolid, Paseo Belén 19, 47011, Valladolid, Spain.

出版信息

Biomacromolecules. 2021 Jan 11;22(1):158-170. doi: 10.1021/acs.biomac.0c00934. Epub 2020 Sep 8.

Abstract

Intrinsically disordered protein polymers (IDPPs) have attracted a lot of attention in the development of bioengineered devices and for use as study models in molecular biology because of their biomechanical properties and stimuli-responsiveness. The present study aims to understand the effect of charge density on the self-assembly of IDPPs. To that end, a library of recombinant IDPPs based on an amphiphilic diblock design with different charge densities was bioproduced, and their supramolecular assembly was characterized on the nano-, meso-, and microscale. Although the phase transition was driven by the collapse of hydrophobic moieties, the hydrophilic block composition strongly affected hierarchical assembly and, therefore, enabled the production of new molecular architectures, thus leading to new dynamics that govern the liquid-gel transition. These results highlight the importance of electrostatic repulsion for the hierarchical assembly of IDPPs and provide insights into the manufacture of supramolecular protein-based materials.

摘要

无规蛋白聚合物 (IDPPs) 因其生物力学特性和对刺激的响应性,在生物工程器件的开发和作为分子生物学研究模型方面引起了广泛关注。本研究旨在了解电荷密度对 IDPPs 自组装的影响。为此,构建了一个基于两亲性嵌段设计的具有不同电荷密度的重组 IDPP 文库,并在纳米、介观和微观尺度上对其超分子组装进行了表征。尽管相转变是由疏水性部分的塌陷驱动的,但亲水性嵌段组成强烈影响了分层组装,从而能够生产新的分子结构,从而导致控制液-凝胶转变的新动力学。这些结果强调了静电排斥对 IDPPs 分层组装的重要性,并为基于蛋白质的超分子材料的制造提供了新的见解。

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