Center for Bio/Molecular Science and Engineering, Code 6900, U.S. Naval Research Laboratory, Washington, District of Columbia, United States of America.
College of Science, George Mason University, Fairfax, Virginia, United States of America.
PLoS One. 2022 Mar 17;17(3):e0265274. doi: 10.1371/journal.pone.0265274. eCollection 2022.
Cell-free protein synthesis systems (CFPS) utilize cellular transcription and translation (TX-TL) machinery to synthesize proteins in vitro. These systems are useful for multiple applications including production of difficult proteins, as high-throughput tools for genetic circuit screening, and as systems for biosensor development. Though rapidly evolving, CFPS suffer from some disadvantages such as limited reaction rates due to longer diffusion times, significant cost per assay when using commercially sourced materials, and reduced reagent stability over prolonged periods. To address some of these challenges, we conducted a series of proof-of-concept experiments to demonstrate enhancement of CFPS productivity via nanoparticle assembly driven nanoaggregation of its constituent proteins. We combined a commercially available CFPS that utilizes purified polyhistidine-tagged (His-tag) TX-TL machinery with CdSe/CdS/ZnS core/shell/shell quantum dots (QDs) known to readily coordinate His-tagged proteins in an oriented fashion. We show that nanoparticle scaffolding of the CFPS cross-links the QDs into nanoaggregate structures while enhancing the production of functional recombinant super-folder green fluorescent protein and phosphotriesterase, an organophosphate hydrolase; the latter by up to 12-fold. This enhancement, which occurs by an undetermined mechanism, has the potential to improve CFPS in general and specifically CFPS-based biosensors (faster response time) while also enabling rapid detoxification/bioremediation through point-of-concern synthesis of similar catalytic enzymes. We further show that such nanoaggregates improve production in diluted CFPS reactions, which can help to save money and extend the amount of these costly reagents. The results are discussed in the context of what may contribute mechanistically to the enhancement and how this can be applied to other CFPS application scenarios.
无细胞蛋白质合成系统(CFPS)利用细胞转录和翻译(TX-TL)机制在体外合成蛋白质。这些系统有多种用途,包括生产困难的蛋白质、作为遗传电路筛选的高通量工具,以及作为生物传感器开发的系统。尽管 CFPS 发展迅速,但也存在一些缺点,例如由于扩散时间较长,反应速率有限,使用商业来源的材料进行每次测定的成本较高,以及在较长时间内试剂稳定性降低。为了解决其中的一些挑战,我们进行了一系列概念验证实验,以证明通过纳米颗粒组装驱动其组成蛋白质的纳米聚集来提高 CFPS 的生产力。我们将一种商业上可用的 CFPS 与 CdSe/CdS/ZnS 核/壳/壳量子点(QD)结合使用,后者已知以定向方式与 His 标记的蛋白质很好地配位。我们表明,CFPS 的纳米颗粒支架将 QD 交联成纳米聚集体结构,同时增强了功能重组超折叠绿色荧光蛋白和有机磷水解酶(磷酸三酯酶)的生产;后者的产量增加了 12 倍。这种增强是通过一种不确定的机制发生的,有可能普遍提高 CFPS 的性能,特别是基于 CFPS 的生物传感器(更快的响应时间),同时通过在关注点合成类似的催化酶来实现快速解毒/生物修复。我们进一步表明,这种纳米聚集体可以提高稀释 CFPS 反应中的产量,从而有助于节省成本并延长这些昂贵试剂的使用时间。结果在可能对增强有机械贡献的方面进行了讨论,以及如何将其应用于其他 CFPS 应用场景。