小体可溶性叶蝉蛋白的细胞外表达。

IF 3.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
ACS Synthetic Biology Pub Date : 2025-03-21 Epub Date: 2025-03-07 DOI:10.1021/acssynbio.4c00773
Caleb G Lay, Gabriel R Burks, Zheng Li, Jeffrey E Barrick, Charles M Schroeder, Ashty S Karim, Michael C Jewett
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引用次数: 0

摘要

溴小体是由叶蝉昆虫产生的具有超疏水和抗反射特性的蛋白质纳米结构。不幸的是,由于对其主要组成亚基蛋白(称为brochosomins)的了解不足,以及由于必需的二硫键对氧化还原条件的敏感性,基于brochosomins的材料的生产和研究受到限制。在这里,我们使用无细胞基因表达(CFE)来实现brochosomin蛋白的重组生产和分析。通过对氧化还原环境、反应温度和二硫键异构酶浓度的优化,可获得可溶性溴酰somin的产率高达341±30 μg/mL。动态光散射和透射电镜分析显示,不同表达的brochosomin在无细胞混合物中具有不同的聚集模式。我们预计,这里开发的CFE方法将加速改变天然和修饰的染色体的几何形状和性质的能力,以及促进其他不太了解的蛋白质复合物的表达和结构分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cell-Free Expression of Soluble Leafhopper Proteins from Brochosomes.

Brochosomes are proteinaceous nanostructures produced by leafhopper insects with superhydrophobic and antireflective properties. Unfortunately, the production and study of brochosome-based materials has been limited by poor understanding of their major constituent subunit proteins, known as brochosomins, as well as their sensitivity to redox conditions due to essential disulfide bonds. Here, we used cell-free gene expression (CFE) to achieve recombinant production and analysis of brochosomin proteins. Through the optimization of redox environment, reaction temperature, and disulfide bond isomerase concentration, we achieved soluble brochosomin yields of up to 341 ± 30 μg/mL. Analysis using dynamic light scattering and transmission electron microscopy revealed distinct aggregation patterns among cell-free mixtures with different expressed brochosomins. We anticipate that the CFE methods developed here will accelerate the ability to change the geometries and properties of natural and modified brochosomes, as well as facilitate the expression and structural analysis of other poorly understood protein complexes.

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来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
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