Gengenbach Benjamin Bruno, Opdensteinen Patrick, Buyel Johannes Felix
Fraunhofer Institute for Molecular Biology and Applied Ecology IME, Aachen, Germany.
Institute for Molecular Biotechnology, RWTH Aachen University, Aachen, Germany.
Front Bioeng Biotechnol. 2020 May 5;8:393. doi: 10.3389/fbioe.2020.00393. eCollection 2020.
The high-throughput screening of recombinant protein expression is advantageous during early process development because it allows the identification of optimal expression constructs and process conditions. Simple screening platforms based on microtiter plates are available for microbes and animal cells, but this was not possible for plants until the development of plant cell packs (PCPs), also known as "cookies," which provide a versatile and scalable screening tool for recombinant protein production. PCPs are prepared from plant cell suspension cultures by removing the medium and molding the biomass. PCPs can be cast into 96-well plates for high-throughput screening, but the manual handling effort currently limits the throughput to ∼500 samples per day. We have therefore integrated the PCP method with a fully automated laboratory liquid-handling station. The "robot cookies" can be prepared and infiltrated with by centrifugation, minimizing operator handling and reducing the likelihood of errors during repeated runs, such as those required in a design of experiments approach. The accumulation of fluorescent protein in the cytosol, apoplast, endoplasmic reticulum or plastids is easily detected using an integrated plate reader, reducing the inter-experimental variation to <5%. We also developed a detergent-based chemical lysis method for protein extraction in a 96-well format, which was adapted for automated downstream processing using miniaturized columns allowing subsequent protein analysis. The new automated method reduces the costs of the platform to <0.5 € per PCP infiltration (a saving of >50%) and facilitates a five-fold increase in throughput to >2500 samples per day.
重组蛋白表达的高通量筛选在早期工艺开发过程中具有优势,因为它能够识别最佳表达构建体和工艺条件。基于微孔板的简单筛选平台可用于微生物和动物细胞,但在植物细胞包(PCP),即所谓的“曲奇”开发出来之前,植物无法使用这种平台。植物细胞包为重组蛋白生产提供了一种通用且可扩展的筛选工具。植物细胞包是通过去除植物细胞悬浮培养物中的培养基并将生物质成型而制备的。植物细胞包可以浇铸到96孔板中进行高通量筛选,但目前的人工操作限制了每天的通量约为500个样本。因此,我们将植物细胞包方法与全自动实验室液体处理工作站集成在一起。“机器人曲奇”可以通过离心制备并接种,最大限度地减少操作人员的操作,并降低重复运行(如实验设计方法所需的运行)过程中出错的可能性。使用集成酶标仪可以轻松检测荧光蛋白在细胞质、质外体、内质网或质体中的积累,将实验间的变异降低到<5%。我们还开发了一种基于去污剂的化学裂解方法,用于96孔板形式的蛋白质提取,该方法适用于使用小型化柱的自动化下游处理,以便随后进行蛋白质分析。这种新的自动化方法将该平台的成本降低到每个植物细胞包接种<0.5欧元(节省>50%),并使通量提高了五倍,达到每天>2500个样本。