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由混合群体的病毒样颗粒自组装而成的多层有序蛋白质阵列。

Multilayered Ordered Protein Arrays Self-Assembled from a Mixed Population of Virus-like Particles.

作者信息

Uchida Masaki, Brunk Nicholas E, Hewagama Nathasha D, Lee Byeongdu, Prevelige Peter E, Jadhao Vikram, Douglas Trevor

机构信息

Department of Chemistry and Biochemistry, California State University, Fresno, 2555 E. San Ramon Avenue, Fresno, California 93740, United States.

Department of Chemistry, Indiana University, 800 E. Kirkwood Avenue, Bloomington, Indiana 47405, United States.

出版信息

ACS Nano. 2022 May 24;16(5):7662-7673. doi: 10.1021/acsnano.1c11272. Epub 2022 May 12.

Abstract

Biology shows many examples of spatially controlled assembly of cells and biomacromolecules into hierarchically organized structures, to which many of the complex biological functions are attributed. While such biological structures have inspired the design of synthetic materials, it is still a great challenge to control the spatial arrangement of individual building blocks when assembling multiple types of components into bulk materials. Here, we report self-assembly of multilayered, ordered protein arrays from mixed populations of virus-like particles (VLPs). We systematically tuned the magnitude of the surface charge of the VLPs via mutagenesis to prepare four different types of VLPs for mixing. A mixture of up to four types of VLPs selectively assembled into higher-order structures in the presence of oppositely charged dendrimers during a gradual lowering of the ionic strength of the solution. The assembly resulted in the formation of three-dimensional ordered VLP arrays with up to four distinct layers including a central core, with each layer comprising a single type of VLP. A coarse-grained computational model was developed and simulated using molecular dynamics to probe the formation of the multilayered, core-shell structure. Our findings establish a simple and versatile bottom-up strategy to synthesize multilayered, ordered materials by controlling the spatial arrangement of multiple types of nanoscale building blocks in a one-pot fabrication.

摘要

生物学展示了许多细胞和生物大分子在空间上受控组装成层次有序结构的例子,许多复杂的生物学功能都归因于这些结构。虽然此类生物结构启发了合成材料的设计,但在将多种类型的组件组装成块状材料时,控制单个构件的空间排列仍然是一项巨大的挑战。在此,我们报告了由混合的病毒样颗粒(VLP)群体自组装形成多层有序蛋白质阵列。我们通过诱变系统地调节了VLP表面电荷的大小,以制备四种不同类型的VLP用于混合。在溶液离子强度逐渐降低的过程中,多达四种类型的VLP混合物在带相反电荷的树枝状聚合物存在下选择性地组装成高阶结构。组装导致形成三维有序的VLP阵列,其具有多达四个不同的层,包括一个中心核,每层由单一类型的VLP组成。我们开发了一个粗粒度计算模型,并使用分子动力学进行模拟,以探究多层核壳结构的形成。我们的研究结果建立了一种简单且通用的自下而上策略,通过在一锅法制备中控制多种类型纳米级构件的空间排列来合成多层有序材料。

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